Cherubism—clinical picture and treatment
Identifieur interne : 007084 ( Istex/Corpus ); précédent : 007083; suivant : 007085Cherubism—clinical picture and treatment
Auteurs : M. Kozakiewicz ; W. Perczynska-Partyka ; J. KobosSource :
- Oral Diseases [ 1354-523X ] ; 2001-03.
English descriptors
- KwdEn :
- Alkaline phosphatase, Autosomal, Autosomal recessive pattern, Blood serum, Brous, Brous displasia, Brous stroma, Case record, Central giant cell granuloma, Cherubic lesions, Cherubism, Clinical comparison, Czas stomat, Diagnostic imaging, Emotional disturbances, Facial, Giant cell tumour, Granulation tissue, Health care centre, Hitomi, Initial examination, Kozakiewicz, Laboratory tests, Lesion, Lodz, Mandible, Mandibular, Mandibular angle, Mandibular angles, Mandibular body, Maxilla, Maxillary sinuses, Maxillofacial surgery, Medical university, Multinucleated giant cells, Oral diseases, Oral diseases picture, Oral maxillofac surg, Oral pathol, Oral surg, Pathologic, Pathologic fracture, Pathologic tissue, Radiological point, Riefkohl, Right bulb displacement, Surg, Surgical intervention.
- Teeft :
- Alkaline phosphatase, Autosomal, Autosomal recessive pattern, Blood serum, Brous, Brous displasia, Brous stroma, Case record, Central giant cell granuloma, Cherubic lesions, Cherubism, Clinical comparison, Czas stomat, Diagnostic imaging, Emotional disturbances, Facial, Giant cell tumour, Granulation tissue, Health care centre, Hitomi, Initial examination, Kozakiewicz, Laboratory tests, Lesion, Lodz, Mandible, Mandibular, Mandibular angle, Mandibular angles, Mandibular body, Maxilla, Maxillary sinuses, Maxillofacial surgery, Medical university, Multinucleated giant cells, Oral diseases, Oral diseases picture, Oral maxillofac surg, Oral pathol, Oral surg, Pathologic, Pathologic fracture, Pathologic tissue, Radiological point, Riefkohl, Right bulb displacement, Surg, Surgical intervention.
Abstract
Cherubism is a rare, painless, disfigurating disease primarily affecting bones of the jaws. OBJECTIVE: To report on five patients with cherubism. The symptoms of the disease, methods of management and possible mode of inheritance are discussed and literature is reviewed. PATIENTS: The study involves five cherubs, members of one family. The diagnoses were based on history, physical examination, laboratory tests, X‐ray parameters, and clinical follow‐up. One member of the family had surgical intervention. The remaining cases were left for observation. RESULTS: Good aesthetic and long lasting effect was reached in the operated patient. CONCLUSIONS: Treatment is unnecessary unless functional or emotional disturbances develop. An autosomal recessive pattern of inheritance is suggested for these cases, although autosomal dominant transmission has been previously established.
Url:
DOI: 10.1034/j.1601-0825.2001.70211.x
Links to Exploration step
ISTEX:E306C2B92ECC07BEBB1CB3A89E48C392C526A132Le document en format XML
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Kobos</name><affiliation><mods:affiliation>Laboratory of Patomorphology, Institute of Pediatry, and Chair and Department of Patomorphology Medical University of Lodz, UI. Sporna 36/50, PL‐91738 Lodz, Poland</mods:affiliation></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">ISTEX</idno><idno type="RBID">ISTEX:E306C2B92ECC07BEBB1CB3A89E48C392C526A132</idno><date when="2001" year="2001">2001</date><idno type="doi">10.1034/j.1601-0825.2001.70211.x</idno><idno type="url">https://api.istex.fr/document/E306C2B92ECC07BEBB1CB3A89E48C392C526A132/fulltext/pdf</idno><idno type="wicri:Area/Istex/Corpus">007084</idno><idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Corpus" wicri:corpus="ISTEX">007084</idno></publicationStmt><sourceDesc><biblStruct><analytic><title level="a" type="main">Cherubism—clinical picture and treatment</title><author><name sortKey="Kozakiewicz, M" sort="Kozakiewicz, M" uniqKey="Kozakiewicz M" first="M" last="Kozakiewicz">M. Kozakiewicz</name><affiliation><mods:affiliation>Clinic of Maxillofacial Surgery, Institute of Dentistry, Medical University of Lodz, Kopcinskiego 22 PL‐90153 Lodz, Poland;</mods:affiliation></affiliation></author><author><name sortKey="Perczynska Artyka, W" sort="Perczynska Artyka, W" uniqKey="Perczynska Artyka W" first="W" last="Perczynska-Partyka">W. Perczynska-Partyka</name><affiliation><mods:affiliation>Clinic of Maxillofacial Surgery, Institute of Dentistry, Medical University of Lodz, Kopcinskiego 22 PL‐90153 Lodz, Poland;</mods:affiliation></affiliation></author><author><name sortKey="Kobos, J" sort="Kobos, J" uniqKey="Kobos J" first="J" last="Kobos">J. Kobos</name><affiliation><mods:affiliation>Laboratory of Patomorphology, Institute of Pediatry, and Chair and Department of Patomorphology Medical University of Lodz, UI. Sporna 36/50, PL‐91738 Lodz, Poland</mods:affiliation></affiliation></author></analytic><monogr></monogr><series><title level="j" type="main">Oral Diseases</title><title level="j" type="alt">ORAL DISEASES</title><idno type="ISSN">1354-523X</idno><idno type="eISSN">1601-0825</idno><imprint><biblScope unit="vol">7</biblScope><biblScope unit="issue">2</biblScope><biblScope unit="page" from="123">123</biblScope><biblScope unit="page" to="130">130</biblScope><biblScope unit="page-count">8</biblScope><publisher>Munksgaard International Publishers</publisher><pubPlace>Oxford, UK</pubPlace><date type="published" when="2001-03">2001-03</date></imprint><idno type="ISSN">1354-523X</idno></series></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">1354-523X</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Alkaline phosphatase</term><term>Autosomal</term><term>Autosomal recessive pattern</term><term>Blood serum</term><term>Brous</term><term>Brous displasia</term><term>Brous stroma</term><term>Case record</term><term>Central giant cell granuloma</term><term>Cherubic lesions</term><term>Cherubism</term><term>Clinical comparison</term><term>Czas stomat</term><term>Diagnostic imaging</term><term>Emotional disturbances</term><term>Facial</term><term>Giant cell tumour</term><term>Granulation tissue</term><term>Health care centre</term><term>Hitomi</term><term>Initial examination</term><term>Kozakiewicz</term><term>Laboratory tests</term><term>Lesion</term><term>Lodz</term><term>Mandible</term><term>Mandibular</term><term>Mandibular angle</term><term>Mandibular angles</term><term>Mandibular body</term><term>Maxilla</term><term>Maxillary sinuses</term><term>Maxillofacial surgery</term><term>Medical university</term><term>Multinucleated giant cells</term><term>Oral diseases</term><term>Oral diseases picture</term><term>Oral maxillofac surg</term><term>Oral pathol</term><term>Oral surg</term><term>Pathologic</term><term>Pathologic fracture</term><term>Pathologic tissue</term><term>Radiological point</term><term>Riefkohl</term><term>Right bulb displacement</term><term>Surg</term><term>Surgical intervention</term></keywords><keywords scheme="Teeft" xml:lang="en"><term>Alkaline phosphatase</term><term>Autosomal</term><term>Autosomal recessive pattern</term><term>Blood serum</term><term>Brous</term><term>Brous displasia</term><term>Brous stroma</term><term>Case record</term><term>Central giant cell granuloma</term><term>Cherubic lesions</term><term>Cherubism</term><term>Clinical comparison</term><term>Czas stomat</term><term>Diagnostic imaging</term><term>Emotional disturbances</term><term>Facial</term><term>Giant cell tumour</term><term>Granulation tissue</term><term>Health care centre</term><term>Hitomi</term><term>Initial examination</term><term>Kozakiewicz</term><term>Laboratory tests</term><term>Lesion</term><term>Lodz</term><term>Mandible</term><term>Mandibular</term><term>Mandibular angle</term><term>Mandibular angles</term><term>Mandibular body</term><term>Maxilla</term><term>Maxillary sinuses</term><term>Maxillofacial surgery</term><term>Medical university</term><term>Multinucleated giant cells</term><term>Oral diseases</term><term>Oral diseases picture</term><term>Oral maxillofac surg</term><term>Oral pathol</term><term>Oral surg</term><term>Pathologic</term><term>Pathologic fracture</term><term>Pathologic tissue</term><term>Radiological point</term><term>Riefkohl</term><term>Right bulb displacement</term><term>Surg</term><term>Surgical intervention</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Cherubism is a rare, painless, disfigurating disease primarily affecting bones of the jaws. OBJECTIVE: To report on five patients with cherubism. The symptoms of the disease, methods of management and possible mode of inheritance are discussed and literature is reviewed. PATIENTS: The study involves five cherubs, members of one family. The diagnoses were based on history, physical examination, laboratory tests, X‐ray parameters, and clinical follow‐up. One member of the family had surgical intervention. The remaining cases were left for observation. RESULTS: Good aesthetic and long lasting effect was reached in the operated patient. CONCLUSIONS: Treatment is unnecessary unless functional or emotional disturbances develop. An autosomal recessive pattern of inheritance is suggested for these cases, although autosomal dominant transmission has been previously established.</div></front></TEI><istex><corpusName>wiley</corpusName><keywords><teeft><json:string>cherubism</json:string><json:string>mandible</json:string><json:string>surg</json:string><json:string>mandibular</json:string><json:string>hitomi</json:string><json:string>brous</json:string><json:string>oral surg</json:string><json:string>maxilla</json:string><json:string>lodz</json:string><json:string>kozakiewicz</json:string><json:string>case record</json:string><json:string>autosomal</json:string><json:string>riefkohl</json:string><json:string>oral maxillofac surg</json:string><json:string>maxillofacial surgery</json:string><json:string>medical university</json:string><json:string>brous stroma</json:string><json:string>pathologic</json:string><json:string>mandibular angles</json:string><json:string>brous displasia</json:string><json:string>oral diseases picture</json:string><json:string>central giant cell granuloma</json:string><json:string>giant cell tumour</json:string><json:string>blood serum</json:string><json:string>multinucleated giant cells</json:string><json:string>oral pathol</json:string><json:string>lesion</json:string><json:string>granulation tissue</json:string><json:string>right bulb displacement</json:string><json:string>mandibular angle</json:string><json:string>initial examination</json:string><json:string>surgical intervention</json:string><json:string>cherubic lesions</json:string><json:string>emotional disturbances</json:string><json:string>maxillary sinuses</json:string><json:string>radiological point</json:string><json:string>clinical comparison</json:string><json:string>oral diseases</json:string><json:string>alkaline phosphatase</json:string><json:string>pathologic fracture</json:string><json:string>pathologic tissue</json:string><json:string>diagnostic imaging</json:string><json:string>autosomal recessive pattern</json:string><json:string>laboratory tests</json:string><json:string>health care centre</json:string><json:string>mandibular body</json:string><json:string>czas stomat</json:string><json:string>facial</json:string></teeft></keywords><author><json:item><name>M Kozakiewicz</name><affiliations><json:string>Clinic of Maxillofacial Surgery, Institute of Dentistry, Medical University of Lodz, Kopcinskiego 22 PL‐90153 Lodz, Poland;</json:string></affiliations></json:item><json:item><name>W Perczynska‐Partyka</name><affiliations><json:string>Clinic of Maxillofacial Surgery, Institute of Dentistry, Medical University of Lodz, Kopcinskiego 22 PL‐90153 Lodz, Poland;</json:string></affiliations></json:item><json:item><name>J Kobos</name><affiliations><json:string>Laboratory of Patomorphology, Institute of Pediatry, and Chair and Department of Patomorphology Medical University of Lodz, UI. Sporna 36/50, PL‐91738 Lodz, Poland</json:string></affiliations></json:item></author><subject><json:item><lang><json:string>eng</json:string></lang><value>cherubism</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>inheritance</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>treatment</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>literature review</value></json:item></subject><articleId><json:string>ODI0070211</json:string></articleId><arkIstex>ark:/67375/WNG-1LCFXQCQ-P</arkIstex><language><json:string>eng</json:string></language><originalGenre><json:string>caseStudy</json:string></originalGenre><abstract>Cherubism is a rare, painless, disfigurating disease primarily affecting bones of the jaws. OBJECTIVE: To report on five patients with cherubism. The symptoms of the disease, methods of management and possible mode of inheritance are discussed and literature is reviewed. PATIENTS: The study involves five cherubs, members of one family. The diagnoses were based on history, physical examination, laboratory tests, X‐ray parameters, and clinical follow‐up. One member of the family had surgical intervention. The remaining cases were left for observation. RESULTS: Good aesthetic and long lasting effect was reached in the operated patient. CONCLUSIONS: Treatment is unnecessary unless functional or emotional disturbances develop. An autosomal recessive pattern of inheritance is suggested for these cases, although autosomal dominant transmission has been previously established.</abstract><qualityIndicators><score>7.217</score><pdfWordCount>3753</pdfWordCount><pdfCharCount>23185</pdfCharCount><pdfVersion>1.2</pdfVersion><pdfPageCount>8</pdfPageCount><pdfPageSize>598 x 796 pts</pdfPageSize><refBibsNative>true</refBibsNative><abstractWordCount>122</abstractWordCount><abstractCharCount>881</abstractCharCount><keywordCount>4</keywordCount></qualityIndicators><title>Cherubism—clinical picture and treatment</title><pmid><json:string>11355438</json:string></pmid><genre><json:string>case-report</json:string></genre><host><title>Oral Diseases</title><language><json:string>unknown</json:string></language><doi><json:string>10.1111/(ISSN)1601-0825</json:string></doi><issn><json:string>1354-523X</json:string></issn><eissn><json:string>1601-0825</json:string></eissn><publisherId><json:string>ODI</json:string></publisherId><volume>7</volume><issue>2</issue><pages><first>123</first><last>130</last><total>8</total></pages><genre><json:string>journal</json:string></genre></host><namedEntities><unitex><date><json:string>2001</json:string><json:string>1954</json:string></date><geogName></geogName><orgName><json:string>Patomorphology Medical University</json:string><json:string>Laboratory of Patomorphology, Institute of Pediatry, and Chair and Department</json:string><json:string>Medical Genetic Institute of Medical University of Lodz</json:string><json:string>Institute of Dentistry of the Medical University of Lodz</json:string><json:string>Japan and Peru</json:string><json:string>Institute of Dentistry, Medical University of Lodz Kopcinskiego</json:string></orgName><orgName_funder></orgName_funder><orgName_provider></orgName_provider><persName><json:string>Ag</json:string><json:string>Davis</json:string><json:string>Surgery</json:string><json:string>Bogdan Kaluzewski</json:string><json:string>Sex</json:string><json:string>Marcin Kozakiewicz</json:string><json:string>Ar</json:string></persName><placeName><json:string>Poland</json:string><json:string>Lodz</json:string><json:string>America</json:string></placeName><ref_url></ref_url><ref_bibl><json:string>Hitomi et al, 1996, 1997</json:string><json:string>Levine et al, 1991</json:string><json:string>Mangion et al (1999)</json:string><json:string>McCledon et al, 1962</json:string><json:string>Hawes, 1989</json:string><json:string>Jones et al (1950)</json:string><json:string>Wackene et al, 1987</json:string><json:string>Riefkohl et al</json:string><json:string>Peters, 1979</json:string><json:string>Arnott, 1978</json:string><json:string>Wada et al, 1996</json:string><json:string>Grunebaum ¨ and Tiqva, 1973</json:string><json:string>Hamner and Ketcham (1969)</json:string><json:string>Hitomi et al, (1996)</json:string><json:string>Lagowska-Adamczyk and Wolanska-Karut, 1994</json:string><json:string>Wells and Sty, 1985</json:string><json:string>Kaugars et al, 1992</json:string><json:string>Mangion et al, 1999</json:string><json:string>Southgate et al (1998)</json:string><json:string>Grunebaum and ¨ Tiqua, 1973</json:string><json:string>Betts et al, 1993</json:string><json:string>Patel, 1987</json:string><json:string>Bianchi et al, 1987</json:string><json:string>McKusik, 1992</json:string><json:string>Marck and Kudryk, 1992</json:string><json:string>Davis et al, 1983</json:string><json:string>Hitomi et al, 1997</json:string><json:string>Suyama and Uragou, 1954</json:string><json:string>Topazian and Costich, 1965</json:string><json:string>Jones, 1933, 1965</json:string><json:string>Zachariades et al, 1985</json:string><json:string>Katz et al, 1992</json:string><json:string>Kozakiewicz et al</json:string><json:string>Morley and Stoneman, 1984</json:string><json:string>Pinborg et al, 1971</json:string><json:string>Jones, 1933</json:string><json:string>Hitomi et al, 1996</json:string><json:string>Rydosz, 1960</json:string><json:string>Caffey and Williams, 1951</json:string><json:string>Faircloth et al, 1991</json:string><json:string>Hart et al, 2000</json:string><json:string>Corduant and Gugny, 1989</json:string><json:string>al Gazali et al, 1993</json:string><json:string>Dubin and Jackson, 1990</json:string><json:string>Riefkohl et al (1985)</json:string><json:string>Zachariades et al (1985)</json:string><json:string>Grunebaum and ¨ Tiqva 1973; Zachariades et al, 1985</json:string><json:string>Southgate et al, 1998</json:string><json:string>Riefkohl et al, 1985</json:string><json:string>Khosla and Korobkin (1970)</json:string></ref_bibl><bibl></bibl></unitex></namedEntities><ark><json:string>ark:/67375/WNG-1LCFXQCQ-P</json:string></ark><categories><wos><json:string>1 - science</json:string><json:string>2 - dentistry, oral surgery & medicine</json:string></wos><scienceMetrix><json:string>1 - health sciences</json:string><json:string>2 - clinical medicine</json:string><json:string>3 - dentistry</json:string></scienceMetrix><scopus><json:string>1 - Health Sciences</json:string><json:string>2 - Dentistry</json:string><json:string>3 - General Dentistry</json:string><json:string>1 - Health Sciences</json:string><json:string>2 - Medicine</json:string><json:string>3 - Otorhinolaryngology</json:string></scopus><inist><json:string>1 - sciences appliquees, technologies et medecines</json:string><json:string>2 - sciences biologiques et medicales</json:string><json:string>3 - sciences medicales</json:string><json:string>4 - pathologie osteoarticulaire</json:string></inist></categories><publicationDate>2001</publicationDate><copyrightDate>2001</copyrightDate><doi><json:string>10.1034/j.1601-0825.2001.70211.x</json:string></doi><id>E306C2B92ECC07BEBB1CB3A89E48C392C526A132</id><score>1</score><fulltext><json:item><extension>pdf</extension><original>true</original><mimetype>application/pdf</mimetype><uri>https://api.istex.fr/document/E306C2B92ECC07BEBB1CB3A89E48C392C526A132/fulltext/pdf</uri></json:item><json:item><extension>zip</extension><original>false</original><mimetype>application/zip</mimetype><uri>https://api.istex.fr/document/E306C2B92ECC07BEBB1CB3A89E48C392C526A132/fulltext/zip</uri></json:item><istex:fulltextTEI uri="https://api.istex.fr/document/E306C2B92ECC07BEBB1CB3A89E48C392C526A132/fulltext/tei"><teiHeader><fileDesc><titleStmt><title level="a" type="main">Cherubism—clinical picture and treatment</title></titleStmt><publicationStmt><authority>ISTEX</authority><publisher>Munksgaard International Publishers</publisher><pubPlace>Oxford, UK</pubPlace><date type="published" when="2001-03"></date></publicationStmt><notesStmt><note type="content-type" subtype="case-report" source="caseStudy" scheme="https://content-type.data.istex.fr/ark:/67375/XTP-29919SZJ-6">case-report</note><note type="publication-type" subtype="journal" scheme="https://publication-type.data.istex.fr/ark:/67375/JMC-0GLKJH51-B">journal</note></notesStmt><sourceDesc><biblStruct type="case-report"><analytic><title level="a" type="main">Cherubism—clinical picture and treatment</title><title level="a" type="short">Cherubism—clinical picture and treatment</title><author xml:id="author-0000"><persName><forename type="first">M</forename><surname>Kozakiewicz</surname></persName><affiliation>Clinic of Maxillofacial Surgery, Institute of Dentistry, Medical University of Lodz, Kopcinskiego 22 PL‐90153 Lodz, Poland;<address><country key="PL"></country></address></affiliation></author><author xml:id="author-0001"><persName><forename type="first">W</forename><surname>Perczynska‐Partyka</surname></persName><affiliation>Clinic of Maxillofacial Surgery, Institute of Dentistry, Medical University of Lodz, Kopcinskiego 22 PL‐90153 Lodz, Poland;<address><country key="PL"></country></address></affiliation></author><author xml:id="author-0002"><persName><forename type="first">J</forename><surname>Kobos</surname></persName><affiliation>Laboratory of Patomorphology, Institute of Pediatry, and Chair and Department of Patomorphology Medical University of Lodz, UI. Sporna 36/50, PL‐91738 Lodz, Poland<address><country key="PL"></country></address></affiliation></author><idno type="istex">E306C2B92ECC07BEBB1CB3A89E48C392C526A132</idno><idno type="ark">ark:/67375/WNG-1LCFXQCQ-P</idno><idno type="DOI">10.1034/j.1601-0825.2001.70211.x</idno><idno type="unit">ODI0070211</idno><idno type="supplier">odi0631</idno><idno type="toTypesetVersion">file:ODI.ODI70211.pdf</idno></analytic><monogr><title level="j" type="main">Oral Diseases</title><title level="j" type="alt">ORAL DISEASES</title><idno type="pISSN">1354-523X</idno><idno type="eISSN">1601-0825</idno><idno type="book-DOI">10.1111/(ISSN)1601-0825</idno><idno type="book-part-DOI">10.1111/odi.2001.7.issue-2</idno><idno type="product">ODI</idno><idno type="publisherDivision">ST</idno><imprint><biblScope unit="vol">7</biblScope><biblScope unit="issue">2</biblScope><biblScope unit="page" from="123">123</biblScope><biblScope unit="page" to="130">130</biblScope><biblScope unit="page-count">8</biblScope><publisher>Munksgaard International Publishers</publisher><pubPlace>Oxford, UK</pubPlace><date type="published" when="2001-03"></date></imprint></monogr></biblStruct></sourceDesc></fileDesc><profileDesc><abstract xml:lang="en" style="main"><p>Cherubism is a rare, painless, disfigurating disease primarily affecting bones of the jaws.</p><p>OBJECTIVE: To report on five patients with cherubism. The symptoms of the disease, methods of management and possible mode of inheritance are discussed and literature is reviewed.</p><p>PATIENTS: The study involves five cherubs, members of one family. The diagnoses were based on history, physical examination, laboratory tests, X‐ray parameters, and clinical follow‐up. One member of the family had surgical intervention. The remaining cases were left for observation.</p><p>RESULTS: Good aesthetic and long lasting effect was reached in the operated patient.</p><p>CONCLUSIONS: Treatment is unnecessary unless functional or emotional disturbances develop. An autosomal recessive pattern of inheritance is suggested for these cases, although autosomal dominant transmission has been previously established.</p></abstract><textClass><keywords xml:lang="en"><term xml:id="k1">cherubism</term><term xml:id="k2">inheritance</term><term xml:id="k3">treatment</term><term xml:id="k4">literature review</term></keywords><keywords rend="tocHeading1"><term>Case Reports</term></keywords></textClass><langUsage><language ident="en"></language></langUsage></profileDesc></teiHeader></istex:fulltextTEI><json:item><extension>txt</extension><original>false</original><mimetype>text/plain</mimetype><uri>https://api.istex.fr/document/E306C2B92ECC07BEBB1CB3A89E48C392C526A132/fulltext/txt</uri></json:item></fulltext><metadata><istex:metadataXml wicri:clean="Wiley, elements deleted: body"><istex:xmlDeclaration>version="1.0" encoding="UTF-8" standalone="yes"</istex:xmlDeclaration><istex:document><component version="2.0" type="serialArticle" xml:lang="en"><header><publicationMeta level="product"><publisherInfo><publisherName>Munksgaard International Publishers</publisherName><publisherLoc>Oxford, UK</publisherLoc></publisherInfo><doi origin="wiley" registered="yes">10.1111/(ISSN)1601-0825</doi><issn type="print">1354-523X</issn><issn type="electronic">1601-0825</issn><idGroup><id type="product" value="ODI"></id><id type="publisherDivision" value="ST"></id></idGroup><titleGroup><title type="main" sort="ORAL DISEASES">Oral Diseases</title></titleGroup></publicationMeta><publicationMeta level="part" position="03002"><doi origin="wiley">10.1111/odi.2001.7.issue-2</doi><numberingGroup><numbering type="journalVolume" number="7">7</numbering><numbering type="journalIssue" number="2">2</numbering></numberingGroup><coverDate startDate="2001-03">March 2001</coverDate></publicationMeta><publicationMeta level="unit" type="caseStudy" position="0012300" status="forIssue"><doi origin="wiley">10.1034/j.1601-0825.2001.70211.x</doi><idGroup><id type="unit" value="ODI0070211"></id><id type="supplier" value="odi0631"></id></idGroup><countGroup><count type="pageTotal" number="8"></count></countGroup><titleGroup><title type="tocHeading1">Case Reports</title></titleGroup><eventGroup><event type="firstOnline" date="2008-07-07"></event><event type="publishedOnlineFinalForm" date="2008-07-07"></event><event type="xmlConverted" agent="Converter:BPG_TO_WML3G version:2.3.2 mode:FullText source:FullText result:FullText" date="2010-03-10"></event><event type="xmlConverted" agent="Converter:WILEY_ML3G_TO_WILEY_ML3GV2 version:3.8.8" date="2014-02-06"></event><event type="xmlConverted" agent="Converter:WML3G_To_WML3G version:4.1.7 mode:FullText,remove_FC" date="2014-11-03"></event></eventGroup><numberingGroup><numbering type="pageFirst" number="123">123</numbering><numbering type="pageLast" number="130">130</numbering></numberingGroup><correspondenceTo>Marcin Kozakiewicz, D.D.S., Ph.D, Clinic of Maxillofacial Surgery, Institute of Dentistry, Medical University of Lodz Kopcinskiego 22, PL‐90153 Lodz, Poland. Fax 0048 42 656 6547</correspondenceTo><linkGroup><link type="toTypesetVersion" href="file:ODI.ODI70211.pdf"></link></linkGroup></publicationMeta><contentMeta><unparsedEditorialHistory>Received 10 May 1999; revised 24 November 1999, 22 May 2000 and 31 July 2000; accepted 9 August 2000</unparsedEditorialHistory><countGroup><count type="figureTotal" number="15"></count><count type="tableTotal" number="2"></count><count type="formulaTotal" number="0"></count><count type="referenceTotal" number="42"></count><count type="wordTotal" number="22775"></count><count type="linksPubMed" number="27"></count><count type="linksCrossRef" number="1"></count></countGroup><titleGroup><title type="main">Cherubism—clinical picture and treatment</title><title type="shortAuthors">M Kozakiewicz <i>et al</i></title><title type="short">Cherubism—clinical picture and treatment</title></titleGroup><creators><creator creatorRole="author" xml:id="cr1" affiliationRef="#a1"><personName><givenNames>M</givenNames><familyName>Kozakiewicz</familyName></personName></creator><creator creatorRole="author" xml:id="cr2" affiliationRef="#a1"><personName><givenNames>W</givenNames><familyName>Perczynska‐Partyka</familyName></personName></creator><creator creatorRole="author" xml:id="cr3" affiliationRef="#a2"><personName><givenNames>J</givenNames><familyName>Kobos</familyName></personName></creator></creators><affiliationGroup><affiliation xml:id="a1" countryCode="PL"><unparsedAffiliation>Clinic of Maxillofacial Surgery, Institute of Dentistry, Medical University of Lodz, Kopcinskiego 22 PL‐90153 Lodz, Poland;</unparsedAffiliation></affiliation><affiliation xml:id="a2" countryCode="PL"><unparsedAffiliation>Laboratory of Patomorphology, Institute of Pediatry, and Chair and Department of Patomorphology Medical University of Lodz, UI. Sporna 36/50, PL‐91738 Lodz, Poland</unparsedAffiliation></affiliation></affiliationGroup><keywordGroup xml:lang="en"><keyword xml:id="k1">cherubism</keyword><keyword xml:id="k2">inheritance</keyword><keyword xml:id="k3">treatment</keyword><keyword xml:id="k4">literature review</keyword></keywordGroup><abstractGroup><abstract type="main" xml:lang="en"><p>Cherubism is a rare, painless, disfigurating disease primarily affecting bones of the jaws.</p><p>OBJECTIVE: To report on five patients with cherubism. The symptoms of the disease, methods of management and possible mode of inheritance are discussed and literature is reviewed.</p><p>PATIENTS: The study involves five cherubs, members of one family. The diagnoses were based on history, physical examination, laboratory tests, X‐ray parameters, and clinical follow‐up. One member of the family had surgical intervention. The remaining cases were left for observation.</p><p>RESULTS: Good aesthetic and long lasting effect was reached in the operated patient.</p><p>CONCLUSIONS: Treatment is unnecessary unless functional or emotional disturbances develop. An autosomal recessive pattern of inheritance is suggested for these cases, although autosomal dominant transmission has been previously established.</p></abstract></abstractGroup></contentMeta></header></component></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Cherubism—clinical picture and treatment</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>Cherubism—clinical picture and treatment</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Cherubism—clinical picture and treatment</title></titleInfo><name type="personal"><namePart type="given">M</namePart><namePart type="family">Kozakiewicz</namePart><affiliation>Clinic of Maxillofacial Surgery, Institute of Dentistry, Medical University of Lodz, Kopcinskiego 22 PL‐90153 Lodz, Poland;</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">W</namePart><namePart type="family">Perczynska‐Partyka</namePart><affiliation>Clinic of Maxillofacial Surgery, Institute of Dentistry, Medical University of Lodz, Kopcinskiego 22 PL‐90153 Lodz, Poland;</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">J</namePart><namePart type="family">Kobos</namePart><affiliation>Laboratory of Patomorphology, Institute of Pediatry, and Chair and Department of Patomorphology Medical University of Lodz, UI. Sporna 36/50, PL‐91738 Lodz, Poland</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="case-report" displayLabel="caseStudy" authority="ISTEX" authorityURI="https://content-type.data.istex.fr" valueURI="https://content-type.data.istex.fr/ark:/67375/XTP-29919SZJ-6">case-report</genre><originInfo><publisher>Munksgaard International Publishers</publisher><place><placeTerm type="text">Oxford, UK</placeTerm></place><dateIssued encoding="w3cdtf">2001-03</dateIssued><edition>Received 10 May 1999; revised 24 November 1999, 22 May 2000 and 31 July 2000; accepted 9 August 2000</edition><copyrightDate encoding="w3cdtf">2001</copyrightDate></originInfo><language><languageTerm type="code" authority="rfc3066">en</languageTerm><languageTerm type="code" authority="iso639-2b">eng</languageTerm></language><physicalDescription><extent unit="figures">15</extent><extent unit="tables">2</extent><extent unit="formulas">0</extent><extent unit="references">42</extent><extent unit="linksCrossRef">1</extent><extent unit="words">22775</extent></physicalDescription><abstract lang="en">Cherubism is a rare, painless, disfigurating disease primarily affecting bones of the jaws. OBJECTIVE: To report on five patients with cherubism. The symptoms of the disease, methods of management and possible mode of inheritance are discussed and literature is reviewed. PATIENTS: The study involves five cherubs, members of one family. The diagnoses were based on history, physical examination, laboratory tests, X‐ray parameters, and clinical follow‐up. One member of the family had surgical intervention. The remaining cases were left for observation. RESULTS: Good aesthetic and long lasting effect was reached in the operated patient. CONCLUSIONS: Treatment is unnecessary unless functional or emotional disturbances develop. An autosomal recessive pattern of inheritance is suggested for these cases, although autosomal dominant transmission has been previously established.</abstract><subject lang="en"><genre>keywords</genre><topic>cherubism</topic><topic>inheritance</topic><topic>treatment</topic><topic>literature review</topic></subject><relatedItem type="host"><titleInfo><title>Oral Diseases</title></titleInfo><genre type="journal" authority="ISTEX" authorityURI="https://publication-type.data.istex.fr" valueURI="https://publication-type.data.istex.fr/ark:/67375/JMC-0GLKJH51-B">journal</genre><identifier type="ISSN">1354-523X</identifier><identifier type="eISSN">1601-0825</identifier><identifier type="DOI">10.1111/(ISSN)1601-0825</identifier><identifier type="PublisherID">ODI</identifier><part><date>2001</date><detail type="volume"><caption>vol.</caption><number>7</number></detail><detail type="issue"><caption>no.</caption><number>2</number></detail><extent unit="pages"><start>123</start><end>130</end><total>8</total></extent></part></relatedItem><identifier type="istex">E306C2B92ECC07BEBB1CB3A89E48C392C526A132</identifier><identifier type="ark">ark:/67375/WNG-1LCFXQCQ-P</identifier><identifier type="DOI">10.1034/j.1601-0825.2001.70211.x</identifier><identifier type="ArticleID">ODI0070211</identifier><recordInfo><recordContentSource authority="ISTEX" authorityURI="https://loaded-corpus.data.istex.fr" valueURI="https://loaded-corpus.data.istex.fr/ark:/67375/XBH-L0C46X92-X">wiley</recordContentSource><recordOrigin>Munksgaard International Publishers</recordOrigin></recordInfo></mods><json:item><extension>json</extension><original>false</original><mimetype>application/json</mimetype><uri>https://api.istex.fr/document/E306C2B92ECC07BEBB1CB3A89E48C392C526A132/metadata/json</uri></json:item></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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