Craniosynostosis update 1987
Identifieur interne : 006087 ( Istex/Corpus ); précédent : 006086; suivant : 006088Craniosynostosis update 1987
Auteurs : Jay Cohen Jr. ; John M. Opitz ; James F. Reynolds ; Robert J. GorlinSource :
- American Journal of Medical Genetics [ 0148-7299 ] ; 1988.
Abstract
Information on craniosynostosis in this paper updates “Craniosynostosis: Diagnosis, Evaluation, and Management” (Cohen MM Jr: New York: Raven Press, 1986). It also discusses recent developments that were included in the book but need further explanation or emphasis. Subjects discussed are: epidemiology, etiology, sutural biology, growth and development, neurological and psychosocial aspects, surgery, cloverleaf skulls, craniosynostosis syndromes, and prenatal diagnosis. Under the subject of etiology, fetal head constraint, maternal thyroid disease, calcified cephalohematoma, teratogens, and delayed suture closure and Wormian bones are considered. An updating of 15 cloverleaf skull conditions includes four monogenic disorders, two chromosomal disorders, one disruption, one iatrogenic condition, and seven syndromes of unknown cause. Newly recognized disorders with cloverleaf skull include Beare‐Stevenson cutis gyratum syndrome and Say‐Poznanski syndrome. Craniosynostosis syndromes and associations discussed include acrocraniofacial dysostosis, Apert syndrome, Beare‐Stevenson cutis gyratum syndrome, Calabro syndrome, calvarial hyperostosis, chromosomal craniostenosis, Cole‐Carpenter type osteogenesis imperfecta, Crouzon syndrome, Curry‐Jones syndrome, Curry variant of Carpenter syndrome, cutis aplasia and cranial stenosis, Fontaine‐Farriaux syndrome, Gomex‐López‐Hernández syndrome, Hersh syndrome, hyper‐IgE syndrome and craniostenosis, hypomandibular faciocranial dysostosis, Marfanoid features and craniostenosis, Pfeiffer‐type cardiocranial syndrome, Pfeiffer‐type dolichocephalosyndactyly, and Say‐Barber syndrome.
Url:
DOI: 10.1002/ajmg.1320310514
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<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">Craniosynostosis update 1987</title><author><name sortKey="Cohen Jr, Jay" sort="Cohen Jr, Jay" uniqKey="Cohen Jr J" first="Jay" last="Cohen Jr.">Jay Cohen Jr.</name><affiliation><mods:affiliation>Department of Oral Biology, Faculty of Dentistry, and Department of Pediatrics, Faculty of Medicine, Dalhousie University, Halifax, Nova Scotia, Canada</mods:affiliation></affiliation><affiliation><mods:affiliation>Department of Oral Biology, Faculty of Dentistry, and Department of Pediatrics, Faculty of Medicine, Dalhousie University, 5981 University Avenue, Halifax, Nova Scotia, Canada B3H 3J5</mods:affiliation></affiliation></author><author><name sortKey="Opitz, John M" sort="Opitz, John M" uniqKey="Opitz J" first="John M." last="Opitz">John M. Opitz</name></author><author><name sortKey="Reynolds, James F" sort="Reynolds, James F" uniqKey="Reynolds J" first="James F." last="Reynolds">James F. Reynolds</name></author><author><name sortKey="Gorlin, Robert J" sort="Gorlin, Robert J" uniqKey="Gorlin R" first="Robert J." last="Gorlin">Robert J. Gorlin</name></author></titleStmt><publicationStmt><idno type="wicri:source">ISTEX</idno><idno type="RBID">ISTEX:CE635A8E0B1EF8873F6BE72CAEF52C92B306E128</idno><date when="1988" year="1988">1988</date><idno type="doi">10.1002/ajmg.1320310514</idno><idno type="url">https://api.istex.fr/document/CE635A8E0B1EF8873F6BE72CAEF52C92B306E128/fulltext/pdf</idno><idno type="wicri:Area/Istex/Corpus">006087</idno><idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Corpus" wicri:corpus="ISTEX">006087</idno></publicationStmt><sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">Craniosynostosis update 1987</title><author><name sortKey="Cohen Jr, Jay" sort="Cohen Jr, Jay" uniqKey="Cohen Jr J" first="Jay" last="Cohen Jr.">Jay Cohen Jr.</name><affiliation><mods:affiliation>Department of Oral Biology, Faculty of Dentistry, and Department of Pediatrics, Faculty of Medicine, Dalhousie University, Halifax, Nova Scotia, Canada</mods:affiliation></affiliation><affiliation><mods:affiliation>Department of Oral Biology, Faculty of Dentistry, and Department of Pediatrics, Faculty of Medicine, Dalhousie University, 5981 University Avenue, Halifax, Nova Scotia, Canada B3H 3J5</mods:affiliation></affiliation></author><author><name sortKey="Opitz, John M" sort="Opitz, John M" uniqKey="Opitz J" first="John M." last="Opitz">John M. 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Gorlin</name></author></analytic><monogr></monogr><series><title level="j" type="main">American Journal of Medical Genetics</title><title level="j" type="alt">AMERICAN JOURNAL OF MEDICAL GENETICS</title><idno type="ISSN">0148-7299</idno><idno type="eISSN">1096-8628</idno><imprint><biblScope unit="vol">31</biblScope><biblScope unit="issue">S4</biblScope><biblScope unit="page" from="99">99</biblScope><biblScope unit="page" to="148">148</biblScope><biblScope unit="page-count">50</biblScope><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><pubPlace>New York</pubPlace><date type="published" when="1988">1988</date></imprint><idno type="ISSN">0148-7299</idno></series></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0148-7299</idno></seriesStmt></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Information on craniosynostosis in this paper updates “Craniosynostosis: Diagnosis, Evaluation, and Management” (Cohen MM Jr: New York: Raven Press, 1986). It also discusses recent developments that were included in the book but need further explanation or emphasis. Subjects discussed are: epidemiology, etiology, sutural biology, growth and development, neurological and psychosocial aspects, surgery, cloverleaf skulls, craniosynostosis syndromes, and prenatal diagnosis. Under the subject of etiology, fetal head constraint, maternal thyroid disease, calcified cephalohematoma, teratogens, and delayed suture closure and Wormian bones are considered. An updating of 15 cloverleaf skull conditions includes four monogenic disorders, two chromosomal disorders, one disruption, one iatrogenic condition, and seven syndromes of unknown cause. Newly recognized disorders with cloverleaf skull include Beare‐Stevenson cutis gyratum syndrome and Say‐Poznanski syndrome. Craniosynostosis syndromes and associations discussed include acrocraniofacial dysostosis, Apert syndrome, Beare‐Stevenson cutis gyratum syndrome, Calabro syndrome, calvarial hyperostosis, chromosomal craniostenosis, Cole‐Carpenter type osteogenesis imperfecta, Crouzon syndrome, Curry‐Jones syndrome, Curry variant of Carpenter syndrome, cutis aplasia and cranial stenosis, Fontaine‐Farriaux syndrome, Gomex‐López‐Hernández syndrome, Hersh syndrome, hyper‐IgE syndrome and craniostenosis, hypomandibular faciocranial dysostosis, Marfanoid features and craniostenosis, Pfeiffer‐type cardiocranial syndrome, Pfeiffer‐type dolichocephalosyndactyly, and Say‐Barber 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Opitz</name></json:item><json:item><name>James F. Reynolds</name></json:item><json:item><name>Robert J. Gorlin</name></json:item></author><subject><json:item><lang><json:string>eng</json:string></lang><value>craniosynostosis syndromes</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>cloverleaf skull</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>sutural biology</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>craniofacial biology</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>craniofacial growth and development</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>craniofacial surgery</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>cranial surgery</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>prenatal diagnosis</value></json:item></subject><articleId><json:string>AJMG1320310514</json:string></articleId><language><json:string>eng</json:string></language><originalGenre><json:string>article</json:string></originalGenre><abstract>Information on craniosynostosis in this paper updates “Craniosynostosis: Diagnosis, Evaluation, and Management” (Cohen MM Jr: New York: Raven Press, 1986). It also discusses recent developments that were included in the book but need further explanation or emphasis. Subjects discussed are: epidemiology, etiology, sutural biology, growth and development, neurological and psychosocial aspects, surgery, cloverleaf skulls, craniosynostosis syndromes, and prenatal diagnosis. Under the subject of etiology, fetal head constraint, maternal thyroid disease, calcified cephalohematoma, teratogens, and delayed suture closure and Wormian bones are considered. An updating of 15 cloverleaf skull conditions includes four monogenic disorders, two chromosomal disorders, one disruption, one iatrogenic condition, and seven syndromes of unknown cause. Newly recognized disorders with cloverleaf skull include Beare‐Stevenson cutis gyratum syndrome and Say‐Poznanski syndrome. Craniosynostosis syndromes and associations discussed include acrocraniofacial dysostosis, Apert syndrome, Beare‐Stevenson cutis gyratum syndrome, Calabro syndrome, calvarial hyperostosis, chromosomal craniostenosis, Cole‐Carpenter type osteogenesis imperfecta, Crouzon syndrome, Curry‐Jones syndrome, Curry variant of Carpenter syndrome, cutis aplasia and cranial stenosis, Fontaine‐Farriaux syndrome, Gomex‐López‐Hernández syndrome, Hersh syndrome, hyper‐IgE syndrome and craniostenosis, hypomandibular faciocranial dysostosis, Marfanoid features and craniostenosis, Pfeiffer‐type cardiocranial syndrome, Pfeiffer‐type dolichocephalosyndactyly, and Say‐Barber syndrome.</abstract><qualityIndicators><score>7.208</score><pdfVersion>1.3</pdfVersion><pdfPageSize>486 x 720 pts</pdfPageSize><refBibsNative>true</refBibsNative><abstractCharCount>1638</abstractCharCount><pdfWordCount>16211</pdfWordCount><pdfCharCount>109946</pdfCharCount><pdfPageCount>50</pdfPageCount><abstractWordCount>184</abstractWordCount></qualityIndicators><title>Craniosynostosis update 1987</title><genre><json:string>article</json:string></genre><host><title>American Journal of Medical Genetics</title><language><json:string>unknown</json:string></language><doi><json:string>10.1002/(ISSN)1096-8628</json:string></doi><issn><json:string>0148-7299</json:string></issn><eissn><json:string>1096-8628</json:string></eissn><publisherId><json:string>AJMG</json:string></publisherId><volume>31</volume><issue>S4</issue><pages><first>99</first><last>148</last><total>50</total></pages><genre><json:string>journal</json:string></genre><subject><json:item><value>Article</value></json:item></subject></host><categories><inist><json:string>sciences appliquees, technologies et medecines</json:string><json:string>sciences biologiques et medicales</json:string><json:string>sciences medicales</json:string><json:string>genetique medicale</json:string></inist></categories><publicationDate>1988</publicationDate><copyrightDate>1988</copyrightDate><doi><json:string>10.1002/ajmg.1320310514</json:string></doi><id>CE635A8E0B1EF8873F6BE72CAEF52C92B306E128</id><score>1</score><fulltext><json:item><extension>pdf</extension><original>true</original><mimetype>application/pdf</mimetype><uri>https://api.istex.fr/document/CE635A8E0B1EF8873F6BE72CAEF52C92B306E128/fulltext/pdf</uri></json:item><json:item><extension>zip</extension><original>false</original><mimetype>application/zip</mimetype><uri>https://api.istex.fr/document/CE635A8E0B1EF8873F6BE72CAEF52C92B306E128/fulltext/zip</uri></json:item><istex:fulltextTEI uri="https://api.istex.fr/document/CE635A8E0B1EF8873F6BE72CAEF52C92B306E128/fulltext/tei"><teiHeader><fileDesc><titleStmt><title level="a" type="main" xml:lang="en">Craniosynostosis update 1987</title></titleStmt><publicationStmt><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><pubPlace>New York</pubPlace><availability><licence>Copyright © 1988 Wiley‐Liss, Inc., A Wiley Company</licence></availability><date type="published" when="1988"></date></publicationStmt><notesStmt><note type="content-type" subtype="article" source="article" scheme="https://content-type.data.istex.fr/ark:/67375/XTP-6N5SZHKN-D">article</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="article"><analytic><title level="a" type="main" xml:lang="en">Craniosynostosis update 1987</title><title level="a" type="short" xml:lang="en">Craniosynostosis Update 1987</title><author xml:id="author-0000" role="corresp"><persName><addName>Dr.</addName><genName>Jr.</genName><forename type="first">M. Michael</forename><surname>Cohen</surname></persName><affiliation>Department of Oral Biology, Faculty of Dentistry, and Department of Pediatrics, Faculty of Medicine, Dalhousie University, Halifax, Nova Scotia, Canada<address><country key="CA"></country></address></affiliation><affiliation>Department of Oral Biology, Faculty of Dentistry, and Department of Pediatrics, Faculty of Medicine, Dalhousie University, 5981 University Avenue, Halifax, Nova Scotia, Canada B3H 3J5</affiliation></author><author xml:id="author-0001"><persName><forename type="first">John M.</forename><surname>Opitz</surname></persName></author><author xml:id="author-0002"><persName><forename type="first">James F.</forename><surname>Reynolds</surname></persName></author><author xml:id="author-0003"><persName><forename type="first">Robert J.</forename><surname>Gorlin</surname></persName></author><idno type="istex">CE635A8E0B1EF8873F6BE72CAEF52C92B306E128</idno><idno type="DOI">10.1002/ajmg.1320310514</idno><idno type="unit">AJMG1320310514</idno><idno type="toTypesetVersion">file:AJMG.AJMG1320310514.pdf</idno></analytic><monogr><title level="j" type="main">American Journal of Medical Genetics</title><title level="j" type="alt">AMERICAN JOURNAL OF MEDICAL GENETICS</title><idno type="pISSN">0148-7299</idno><idno type="eISSN">1096-8628</idno><idno type="book-DOI">10.1002/(ISSN)1096-8628</idno><idno type="book-part-DOI">10.1002/ajmg.v31:4+</idno><idno type="product">AJMG</idno><imprint><biblScope unit="vol">31</biblScope><biblScope unit="issue">S4</biblScope><biblScope unit="page" from="99">99</biblScope><biblScope unit="page" to="148">148</biblScope><biblScope unit="page-count">50</biblScope><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><pubPlace>New York</pubPlace><date type="published" when="1988"></date></imprint></monogr></biblStruct></sourceDesc></fileDesc><profileDesc><abstract xml:lang="en" style="main"><head>Abstract</head><p>Information on craniosynostosis in this paper updates “Craniosynostosis: Diagnosis, Evaluation, and Management” (Cohen MM Jr: New York: Raven Press, 1986). It also discusses recent developments that were included in the book but need further explanation or emphasis. Subjects discussed are: epidemiology, etiology, sutural biology, growth and development, neurological and psychosocial aspects, surgery, cloverleaf skulls, craniosynostosis syndromes, and prenatal diagnosis. Under the subject of etiology, fetal head constraint, maternal thyroid disease, calcified cephalohematoma, teratogens, and delayed suture closure and Wormian bones are considered. An updating of 15 cloverleaf skull conditions includes four monogenic disorders, two chromosomal disorders, one disruption, one iatrogenic condition, and seven syndromes of unknown cause. Newly recognized disorders with cloverleaf skull include Beare‐Stevenson cutis gyratum syndrome and Say‐Poznanski syndrome. Craniosynostosis syndromes and associations discussed include acrocraniofacial dysostosis, Apert syndrome, Beare‐Stevenson cutis gyratum syndrome, Calabro syndrome, calvarial hyperostosis, chromosomal craniostenosis, Cole‐Carpenter type osteogenesis imperfecta, Crouzon syndrome, Curry‐Jones syndrome, Curry variant of Carpenter syndrome, cutis aplasia and cranial stenosis, Fontaine‐Farriaux syndrome, Gomex‐López‐Hernández syndrome, Hersh syndrome, hyper‐IgE syndrome and craniostenosis, hypomandibular faciocranial dysostosis, Marfanoid features and craniostenosis, Pfeiffer‐type cardiocranial syndrome, Pfeiffer‐type dolichocephalosyndactyly, and Say‐Barber syndrome.</p></abstract><textClass><keywords xml:lang="en"><term xml:id="kwd1">craniosynostosis syndromes</term><term xml:id="kwd2">cloverleaf skull</term><term xml:id="kwd3">sutural biology</term><term xml:id="kwd4">craniofacial biology</term><term xml:id="kwd5">craniofacial growth and development</term><term xml:id="kwd6">craniofacial surgery</term><term xml:id="kwd7">cranial surgery</term><term xml:id="kwd8">prenatal diagnosis</term></keywords><classCode scheme="articleCategory">Article</classCode><classCode scheme="tocHeading1">Articles</classCode></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/CE635A8E0B1EF8873F6BE72CAEF52C92B306E128/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>Wiley Subscription Services, Inc., A Wiley Company</publisherName><publisherLoc>New York</publisherLoc></publisherInfo><doi registered="yes">10.1002/(ISSN)1096-8628</doi><issn type="print">0148-7299</issn><issn type="electronic">1096-8628</issn><idGroup><id type="product" value="AJMG"></id></idGroup><titleGroup><title type="main" xml:lang="en" sort="AMERICAN JOURNAL OF MEDICAL GENETICS">American Journal of Medical Genetics</title><title type="short">Am. J. Med. Genet.</title></titleGroup></publicationMeta><publicationMeta level="part" position="50"><doi origin="wiley" registered="yes">10.1002/ajmg.v31:4+</doi><titleGroup><title type="supplementTitle">Proceedings of the March of Dimes Clinical Genetics Conference Neural Crest and Craniofacial Disorders</title></titleGroup><numberingGroup><numbering type="journalVolume" number="31">31</numbering><numbering type="journalIssue">S4</numbering><numbering type="supplement" number="S1">S1</numbering></numberingGroup><coverDate startDate="1988">1988</coverDate></publicationMeta><publicationMeta level="unit" type="article" position="14" status="forIssue"><doi origin="wiley" registered="yes">10.1002/ajmg.1320310514</doi><idGroup><id type="unit" value="AJMG1320310514"></id></idGroup><countGroup><count type="pageTotal" number="50"></count></countGroup><titleGroup><title type="articleCategory">Article</title><title type="tocHeading1">Articles</title></titleGroup><copyright ownership="publisher">Copyright © 1988 Wiley‐Liss, Inc., A Wiley Company</copyright><eventGroup><event type="manuscriptReceived" date="1987-06-17"></event><event type="manuscriptRevised" date="1987-08-19"></event><event type="firstOnline" date="2005-06-03"></event><event type="publishedOnlineFinalForm" date="2005-06-03"></event><event type="xmlConverted" agent="Converter:JWSART34_TO_WML3G version:2.3.9 mode:FullText" date="2010-06-24"></event><event type="xmlConverted" agent="Converter:WILEY_ML3G_TO_WILEY_ML3GV2 version:3.8.8" date="2014-01-02"></event><event type="xmlConverted" agent="Converter:WML3G_To_WML3G version:4.1.7 mode:FullText,remove_FC" date="2014-10-14"></event></eventGroup><numberingGroup><numbering type="pageFirst">99</numbering><numbering type="pageLast">148</numbering></numberingGroup><correspondenceTo>Department of Oral Biology, Faculty of Dentistry, and Department of Pediatrics, Faculty of Medicine, Dalhousie University, 5981 University Avenue, Halifax, Nova Scotia, Canada B3H 3J5</correspondenceTo><linkGroup><link type="toTypesetVersion" href="file:AJMG.AJMG1320310514.pdf"></link></linkGroup></publicationMeta><contentMeta><countGroup><count type="figureTotal" number="62"></count><count type="tableTotal" number="7"></count><count type="referenceTotal" number="195"></count></countGroup><titleGroup><title type="main" xml:lang="en">Craniosynostosis update 1987</title><title type="short" xml:lang="en">Craniosynostosis Update 1987</title></titleGroup><creators><creator xml:id="au1" creatorRole="author" affiliationRef="#af1" corresponding="yes"><personName><honorifics>Dr.</honorifics><givenNames>M. Michael</givenNames><familyName>Cohen</familyName><nameSuffix>Jr.</nameSuffix></personName></creator><creator xml:id="au2" creatorRole="author"><personName><givenNames>John M.</givenNames><familyName>Opitz</familyName></personName><jobTitle>Editor</jobTitle></creator><creator xml:id="au3" creatorRole="author"><personName><givenNames>James F.</givenNames><familyName>Reynolds</familyName></personName><jobTitle>Editor</jobTitle></creator><creator xml:id="au4" creatorRole="author"><personName><givenNames>Robert J.</givenNames><familyName>Gorlin</familyName></personName><jobTitle>Editor</jobTitle></creator></creators><affiliationGroup><affiliation xml:id="af1" countryCode="CA" type="organization"><unparsedAffiliation>Department of Oral Biology, Faculty of Dentistry, and Department of Pediatrics, Faculty of Medicine, Dalhousie University, Halifax, Nova Scotia, Canada</unparsedAffiliation></affiliation></affiliationGroup><keywordGroup xml:lang="en" type="author"><keyword xml:id="kwd1">craniosynostosis syndromes</keyword><keyword xml:id="kwd2">cloverleaf skull</keyword><keyword xml:id="kwd3">sutural biology</keyword><keyword xml:id="kwd4">craniofacial biology</keyword><keyword xml:id="kwd5">craniofacial growth and development</keyword><keyword xml:id="kwd6">craniofacial surgery</keyword><keyword xml:id="kwd7">cranial surgery</keyword><keyword xml:id="kwd8">prenatal diagnosis</keyword></keywordGroup><abstractGroup><abstract type="main" xml:lang="en"><title type="main">Abstract</title><p>Information on craniosynostosis in this paper updates “Craniosynostosis: Diagnosis, Evaluation, and Management” (Cohen MM Jr: New York: Raven Press, 1986). It also discusses recent developments that were included in the book but need further explanation or emphasis. Subjects discussed are: epidemiology, etiology, sutural biology, growth and development, neurological and psychosocial aspects, surgery, cloverleaf skulls, craniosynostosis syndromes, and prenatal diagnosis. Under the subject of etiology, fetal head constraint, maternal thyroid disease, calcified cephalohematoma, teratogens, and delayed suture closure and Wormian bones are considered. An updating of 15 cloverleaf skull conditions includes four monogenic disorders, two chromosomal disorders, one disruption, one iatrogenic condition, and seven syndromes of unknown cause. Newly recognized disorders with cloverleaf skull include Beare‐Stevenson cutis gyratum syndrome and Say‐Poznanski syndrome. Craniosynostosis syndromes and associations discussed include acrocraniofacial dysostosis, Apert syndrome, Beare‐Stevenson cutis gyratum syndrome, Calabro syndrome, calvarial hyperostosis, chromosomal craniostenosis, Cole‐Carpenter type osteogenesis imperfecta, Crouzon syndrome, Curry‐Jones syndrome, Curry variant of Carpenter syndrome, cutis aplasia and cranial stenosis, Fontaine‐Farriaux syndrome, Gomex‐López‐Hernández syndrome, Hersh syndrome, hyper‐IgE syndrome and craniostenosis, hypomandibular faciocranial dysostosis, Marfanoid features and craniostenosis, Pfeiffer‐type cardiocranial syndrome, Pfeiffer‐type dolichocephalosyndactyly, and Say‐Barber syndrome.</p></abstract></abstractGroup></contentMeta></header></component></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Craniosynostosis update 1987</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>Craniosynostosis Update 1987</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Craniosynostosis update 1987</title></titleInfo><name type="personal"><namePart type="termsOfAddress">Dr.</namePart><namePart type="family">Cohen Jr.</namePart><affiliation>Department of Oral Biology, Faculty of Dentistry, and Department of Pediatrics, Faculty of Medicine, Dalhousie University, Halifax, Nova Scotia, Canada</affiliation><affiliation>Department of Oral Biology, Faculty of Dentistry, and Department of Pediatrics, Faculty of Medicine, Dalhousie University, 5981 University Avenue, Halifax, Nova Scotia, Canada B3H 3J5</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">John M.</namePart><namePart type="family">Opitz</namePart><role><roleTerm type="text">author</roleTerm></role><description>Editor</description></name><name type="personal"><namePart type="given">James F.</namePart><namePart type="family">Reynolds</namePart><role><roleTerm type="text">author</roleTerm></role><description>Editor</description></name><name type="personal"><namePart type="given">Robert J.</namePart><namePart type="family">Gorlin</namePart><role><roleTerm type="text">author</roleTerm></role><description>Editor</description></name><typeOfResource>text</typeOfResource><genre type="article" displayLabel="article"></genre><originInfo><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><place><placeTerm type="text">New York</placeTerm></place><dateIssued encoding="w3cdtf">1988</dateIssued><dateCaptured encoding="w3cdtf">1987-06-17</dateCaptured><copyrightDate encoding="w3cdtf">1988</copyrightDate></originInfo><language><languageTerm type="code" authority="rfc3066">en</languageTerm><languageTerm type="code" authority="iso639-2b">eng</languageTerm></language><physicalDescription><internetMediaType>text/html</internetMediaType><extent unit="figures">62</extent><extent unit="tables">7</extent><extent unit="references">195</extent></physicalDescription><abstract lang="en">Information on craniosynostosis in this paper updates “Craniosynostosis: Diagnosis, Evaluation, and Management” (Cohen MM Jr: New York: Raven Press, 1986). It also discusses recent developments that were included in the book but need further explanation or emphasis. Subjects discussed are: epidemiology, etiology, sutural biology, growth and development, neurological and psychosocial aspects, surgery, cloverleaf skulls, craniosynostosis syndromes, and prenatal diagnosis. Under the subject of etiology, fetal head constraint, maternal thyroid disease, calcified cephalohematoma, teratogens, and delayed suture closure and Wormian bones are considered. An updating of 15 cloverleaf skull conditions includes four monogenic disorders, two chromosomal disorders, one disruption, one iatrogenic condition, and seven syndromes of unknown cause. Newly recognized disorders with cloverleaf skull include Beare‐Stevenson cutis gyratum syndrome and Say‐Poznanski syndrome. Craniosynostosis syndromes and associations discussed include acrocraniofacial dysostosis, Apert syndrome, Beare‐Stevenson cutis gyratum syndrome, Calabro syndrome, calvarial hyperostosis, chromosomal craniostenosis, Cole‐Carpenter type osteogenesis imperfecta, Crouzon syndrome, Curry‐Jones syndrome, Curry variant of Carpenter syndrome, cutis aplasia and cranial stenosis, Fontaine‐Farriaux syndrome, Gomex‐López‐Hernández syndrome, Hersh syndrome, hyper‐IgE syndrome and craniostenosis, hypomandibular faciocranial dysostosis, Marfanoid features and craniostenosis, Pfeiffer‐type cardiocranial syndrome, Pfeiffer‐type dolichocephalosyndactyly, and Say‐Barber syndrome.</abstract><subject lang="en"><genre>keywords</genre><topic>craniosynostosis syndromes</topic><topic>cloverleaf skull</topic><topic>sutural biology</topic><topic>craniofacial biology</topic><topic>craniofacial growth and development</topic><topic>craniofacial surgery</topic><topic>cranial surgery</topic><topic>prenatal diagnosis</topic></subject><relatedItem type="host"><titleInfo><title>American Journal of Medical Genetics</title></titleInfo><titleInfo type="abbreviated"><title>Am. J. Med. Genet.</title></titleInfo><genre type="journal">journal</genre><subject><genre>article-category</genre><topic>Article</topic></subject><identifier type="ISSN">0148-7299</identifier><identifier type="eISSN">1096-8628</identifier><identifier type="DOI">10.1002/(ISSN)1096-8628</identifier><identifier type="PublisherID">AJMG</identifier><part><date>1988</date><detail type="volume"><caption>vol.</caption><number>31</number></detail><detail type="issue"><caption>no.</caption><number>S4</number></detail><detail type="supplement"><caption>Suppl. no.</caption><number>S1</number></detail><extent unit="pages"><start>99</start><end>148</end><total>50</total></extent></part></relatedItem><identifier type="istex">CE635A8E0B1EF8873F6BE72CAEF52C92B306E128</identifier><identifier type="DOI">10.1002/ajmg.1320310514</identifier><identifier type="ArticleID">AJMG1320310514</identifier><accessCondition type="use and reproduction" contentType="copyright">Copyright © 1988 Wiley‐Liss, Inc., A Wiley Company</accessCondition><recordInfo><recordContentSource>WILEY</recordContentSource><recordOrigin>Wiley Subscription Services, Inc., A Wiley Company</recordOrigin></recordInfo></mods></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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