"Oral Manifestations of Patients with Inherited Defect in Phagocyte Number or Function" a systematic review.
Identifieur interne : 000016 ( Main/Exploration ); précédent : 000015; suivant : 000017"Oral Manifestations of Patients with Inherited Defect in Phagocyte Number or Function" a systematic review.
Auteurs : Heliya Ziaei [Iran] ; Arghavan Tonkaboni [Iran] ; Ahmadreza Shamshiri [Iran] ; Nima Rezaei [Iran]Source :
- Clinical immunology (Orlando, Fla.) [ 1521-7035 ] ; 2021.
Descripteurs français
- KwdFr :
- Déficience en GATA2 (diagnostic), Déficience en GATA2 (génétique), Déficience en GATA2 (immunologie), Femelle (MeSH), Granulomatose septique chronique (diagnostic), Granulomatose septique chronique (génétique), Granulomatose septique chronique (immunologie), Humains (MeSH), Maladie de Papillon-Lefèvre (diagnostic), Maladie de Papillon-Lefèvre (génétique), Maladie de Papillon-Lefèvre (immunologie), Maladies de la bouche (diagnostic), Maladies de la bouche (génétique), Maladies de la bouche (immunologie), Mâle (MeSH), Neutropénie (congénital), Neutropénie (diagnostic), Neutropénie (immunologie), Phagocytes (anatomopathologie), Phagocytes (immunologie), Stimulation du métabolisme oxydatif (génétique), Stimulation du métabolisme oxydatif (immunologie).
- MESH :
- anatomopathologie : Phagocytes.
- congénital : Neutropénie.
- diagnostic : Déficience en GATA2, Granulomatose septique chronique, Maladie de Papillon-Lefèvre, Maladies de la bouche, Neutropénie.
- génétique : Déficience en GATA2, Granulomatose septique chronique, Maladie de Papillon-Lefèvre, Maladies de la bouche, Stimulation du métabolisme oxydatif.
- immunologie : Déficience en GATA2, Granulomatose septique chronique, Maladie de Papillon-Lefèvre, Maladies de la bouche, Neutropénie, Phagocytes, Stimulation du métabolisme oxydatif.
- Femelle, Humains, Mâle.
English descriptors
- KwdEn :
- Female (MeSH), GATA2 Deficiency (diagnosis), GATA2 Deficiency (genetics), GATA2 Deficiency (immunology), Granulomatous Disease, Chronic (diagnosis), Granulomatous Disease, Chronic (genetics), Granulomatous Disease, Chronic (immunology), Humans (MeSH), Male (MeSH), Mouth Diseases (diagnosis), Mouth Diseases (genetics), Mouth Diseases (immunology), Neutropenia (congenital), Neutropenia (diagnosis), Neutropenia (immunology), Papillon-Lefevre Disease (diagnosis), Papillon-Lefevre Disease (genetics), Papillon-Lefevre Disease (immunology), Phagocytes (immunology), Phagocytes (pathology), Primary Immunodeficiency Diseases (diagnosis), Primary Immunodeficiency Diseases (genetics), Primary Immunodeficiency Diseases (immunology), Respiratory Burst (genetics), Respiratory Burst (immunology).
- MESH :
- congenital : Neutropenia.
- diagnosis : GATA2 Deficiency, Granulomatous Disease, Chronic, Mouth Diseases, Neutropenia, Papillon-Lefevre Disease, Primary Immunodeficiency Diseases.
- genetics : GATA2 Deficiency, Granulomatous Disease, Chronic, Mouth Diseases, Papillon-Lefevre Disease, Primary Immunodeficiency Diseases, Respiratory Burst.
- immunology : GATA2 Deficiency, Granulomatous Disease, Chronic, Mouth Diseases, Neutropenia, Papillon-Lefevre Disease, Phagocytes, Primary Immunodeficiency Diseases, Respiratory Burst.
- pathology : Phagocytes.
- Female, Humans, Male.
Abstract
INTRODUCTION
Inherited phagocyte defects are one of the subgroups of primary immunodeficiency diseases (PIDs) with various clinical manifestations. As oral manifestations are common at the early ages, oral practitioners can have a special role in the early diagnosis.
MATERIALS AND METHODS
A comprehensive search was conducted in this systematic review study and data of included studies were categorized into four subgroups of phagocyte defects, including congenital neutropenia, defects of motility, defects of respiratory burst, and other non-lymphoid defects.
RESULTS
Among all phagocyte defects, 12 disorders had reported data for oral manifestations in published articles. A total of 987 cases were included in this study. Periodontitis is one of the most common oral manifestations.
CONCLUSION
There is a need to organize better collaboration between medical doctors and dentists to diagnose and treat patients with phagocyte defects. Regular dental visits and professional oral health care are recommended from the time of the first primary teeth eruption in newborns.
DOI: 10.1016/j.clim.2021.108796
PubMed: 34271191
Affiliations:
Links toward previous steps (curation, corpus...)
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Electronic address: Rezaei_nima@tums.ac.ir.</nlm:affiliation><country xml:lang="fr">Iran</country><wicri:regionArea>Network of Immunity in Infection, Malignancy and Autoimmunity (NIIMA), Universal Scientific Education and Research Network (USERN), Tehran, Iran; Research Center for Immunodeficiencies, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran; Department of Immunology, School of Medicine, Tehran University of Medical Sciences, Tehran</wicri:regionArea><wicri:noRegion>Tehran</wicri:noRegion></affiliation></author></analytic><series><title level="j">Clinical immunology (Orlando, Fla.)</title><idno type="eISSN">1521-7035</idno><imprint><date when="2021" type="published">2021</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Female (MeSH)</term><term>GATA2 Deficiency (diagnosis)</term><term>GATA2 Deficiency (genetics)</term><term>GATA2 Deficiency (immunology)</term><term>Granulomatous Disease, Chronic (diagnosis)</term><term>Granulomatous Disease, Chronic (genetics)</term><term>Granulomatous Disease, Chronic (immunology)</term><term>Humans (MeSH)</term><term>Male (MeSH)</term><term>Mouth Diseases (diagnosis)</term><term>Mouth Diseases (genetics)</term><term>Mouth Diseases (immunology)</term><term>Neutropenia (congenital)</term><term>Neutropenia (diagnosis)</term><term>Neutropenia (immunology)</term><term>Papillon-Lefevre Disease (diagnosis)</term><term>Papillon-Lefevre Disease (genetics)</term><term>Papillon-Lefevre Disease (immunology)</term><term>Phagocytes (immunology)</term><term>Phagocytes (pathology)</term><term>Primary Immunodeficiency Diseases (diagnosis)</term><term>Primary Immunodeficiency Diseases (genetics)</term><term>Primary Immunodeficiency Diseases (immunology)</term><term>Respiratory Burst (genetics)</term><term>Respiratory Burst (immunology)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Déficience en GATA2 (diagnostic)</term><term>Déficience en GATA2 (génétique)</term><term>Déficience en GATA2 (immunologie)</term><term>Femelle (MeSH)</term><term>Granulomatose septique chronique (diagnostic)</term><term>Granulomatose septique chronique (génétique)</term><term>Granulomatose septique chronique (immunologie)</term><term>Humains (MeSH)</term><term>Maladie de Papillon-Lefèvre (diagnostic)</term><term>Maladie de Papillon-Lefèvre (génétique)</term><term>Maladie de Papillon-Lefèvre (immunologie)</term><term>Maladies de la bouche (diagnostic)</term><term>Maladies de la bouche (génétique)</term><term>Maladies de la bouche (immunologie)</term><term>Mâle (MeSH)</term><term>Neutropénie (congénital)</term><term>Neutropénie (diagnostic)</term><term>Neutropénie (immunologie)</term><term>Phagocytes (anatomopathologie)</term><term>Phagocytes (immunologie)</term><term>Stimulation du métabolisme oxydatif (génétique)</term><term>Stimulation du métabolisme oxydatif (immunologie)</term></keywords><keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr"><term>Phagocytes</term></keywords><keywords scheme="MESH" qualifier="congenital" xml:lang="en"><term>Neutropenia</term></keywords><keywords scheme="MESH" qualifier="congénital" xml:lang="fr"><term>Neutropénie</term></keywords><keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>GATA2 Deficiency</term><term>Granulomatous Disease, Chronic</term><term>Mouth Diseases</term><term>Neutropenia</term><term>Papillon-Lefevre Disease</term><term>Primary Immunodeficiency Diseases</term></keywords><keywords scheme="MESH" qualifier="diagnostic" xml:lang="fr"><term>Déficience en GATA2</term><term>Granulomatose septique chronique</term><term>Maladie de Papillon-Lefèvre</term><term>Maladies de la bouche</term><term>Neutropénie</term></keywords><keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>GATA2 Deficiency</term><term>Granulomatous Disease, Chronic</term><term>Mouth Diseases</term><term>Papillon-Lefevre Disease</term><term>Primary Immunodeficiency Diseases</term><term>Respiratory Burst</term></keywords><keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Déficience en GATA2</term><term>Granulomatose septique chronique</term><term>Maladie de Papillon-Lefèvre</term><term>Maladies de la bouche</term><term>Stimulation du métabolisme oxydatif</term></keywords><keywords scheme="MESH" qualifier="immunologie" xml:lang="fr"><term>Déficience en GATA2</term><term>Granulomatose septique chronique</term><term>Maladie de Papillon-Lefèvre</term><term>Maladies de la bouche</term><term>Neutropénie</term><term>Phagocytes</term><term>Stimulation du métabolisme oxydatif</term></keywords><keywords scheme="MESH" qualifier="immunology" xml:lang="en"><term>GATA2 Deficiency</term><term>Granulomatous Disease, Chronic</term><term>Mouth Diseases</term><term>Neutropenia</term><term>Papillon-Lefevre Disease</term><term>Phagocytes</term><term>Primary Immunodeficiency Diseases</term><term>Respiratory Burst</term></keywords><keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Phagocytes</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Female</term><term>Humans</term><term>Male</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Femelle</term><term>Humains</term><term>Mâle</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p><b>INTRODUCTION</b></p><p>Inherited phagocyte defects are one of the subgroups of primary immunodeficiency diseases (PIDs) with various clinical manifestations. As oral manifestations are common at the early ages, oral practitioners can have a special role in the early diagnosis.</p></div><div type="abstract" xml:lang="en"><p><b>MATERIALS AND METHODS</b></p><p>A comprehensive search was conducted in this systematic review study and data of included studies were categorized into four subgroups of phagocyte defects, including congenital neutropenia, defects of motility, defects of respiratory burst, and other non-lymphoid defects.</p></div><div type="abstract" xml:lang="en"><p><b>RESULTS</b></p><p>Among all phagocyte defects, 12 disorders had reported data for oral manifestations in published articles. A total of 987 cases were included in this study. Periodontitis is one of the most common oral manifestations.</p></div><div type="abstract" xml:lang="en"><p><b>CONCLUSION</b></p><p>There is a need to organize better collaboration between medical doctors and dentists to diagnose and treat patients with phagocyte defects. Regular dental visits and professional oral health care are recommended from the time of the first primary teeth eruption in newborns.</p></div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">34271191</PMID><DateCompleted><Year>2021</Year><Month>09</Month><Day>16</Day></DateCompleted><DateRevised><Year>2021</Year><Month>09</Month><Day>16</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1521-7035</ISSN><JournalIssue CitedMedium="Internet"><Volume>229</Volume><PubDate><Year>2021</Year><Month>08</Month></PubDate></JournalIssue><Title>Clinical immunology (Orlando, Fla.)</Title><ISOAbbreviation>Clin Immunol</ISOAbbreviation></Journal><ArticleTitle>"Oral Manifestations of Patients with Inherited Defect in Phagocyte Number or Function" a systematic review.</ArticleTitle><Pagination><MedlinePgn>108796</MedlinePgn></Pagination><ELocationID EIdType="pii" ValidYN="Y">S1521-6616(21)00133-9</ELocationID><ELocationID EIdType="doi" ValidYN="Y">10.1016/j.clim.2021.108796</ELocationID><Abstract><AbstractText Label="INTRODUCTION">Inherited phagocyte defects are one of the subgroups of primary immunodeficiency diseases (PIDs) with various clinical manifestations. As oral manifestations are common at the early ages, oral practitioners can have a special role in the early diagnosis.</AbstractText><AbstractText Label="MATERIALS AND METHODS">A comprehensive search was conducted in this systematic review study and data of included studies were categorized into four subgroups of phagocyte defects, including congenital neutropenia, defects of motility, defects of respiratory burst, and other non-lymphoid defects.</AbstractText><AbstractText Label="RESULTS">Among all phagocyte defects, 12 disorders had reported data for oral manifestations in published articles. A total of 987 cases were included in this study. Periodontitis is one of the most common oral manifestations.</AbstractText><AbstractText Label="CONCLUSION">There is a need to organize better collaboration between medical doctors and dentists to diagnose and treat patients with phagocyte defects. Regular dental visits and professional oral health care are recommended from the time of the first primary teeth eruption in newborns.</AbstractText><CopyrightInformation>Copyright © 2021 Elsevier Inc. All rights reserved.</CopyrightInformation></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Ziaei</LastName><ForeName>Heliya</ForeName><Initials>H</Initials><AffiliationInfo><Affiliation>Faculty of Dentistry, Tehran University of Medical Sciences, Tehran, Iran; Network of Immunity in Infection, Malignancy and Autoimmunity (NIIMA), Universal Scientific Education and Research Network (USERN), Tehran, Iran; Maxillofacial Surgery and Implantology and Biomaterial Research Foundation, Tehran, Iran.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Tonkaboni</LastName><ForeName>Arghavan</ForeName><Initials>A</Initials><AffiliationInfo><Affiliation>Oral & Maxillofacial Medicine Department, School of Dentistry, Tehran University of Medical Sciences, Tehran, Iran.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Shamshiri</LastName><ForeName>Ahmadreza</ForeName><Initials>A</Initials><AffiliationInfo><Affiliation>Research Center for Caries Prevention, Dental Research Institute, Department of Community Oral Health, School of Dentistry, Tehran University of Medical Sciences, Tehran, Iran.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Rezaei</LastName><ForeName>Nima</ForeName><Initials>N</Initials><AffiliationInfo><Affiliation>Network of Immunity in Infection, Malignancy and Autoimmunity (NIIMA), Universal Scientific Education and Research Network (USERN), Tehran, Iran; Research Center for Immunodeficiencies, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran; Department of Immunology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran. Electronic address: Rezaei_nima@tums.ac.ir.</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D000078182">Systematic Review</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2021</Year><Month>07</Month><Day>14</Day></ArticleDate></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>Clin Immunol</MedlineTA><NlmUniqueID>100883537</NlmUniqueID><ISSNLinking>1521-6616</ISSNLinking></MedlineJournalInfo><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D000077428" MajorTopicYN="N">GATA2 Deficiency</DescriptorName><QualifierName UI="Q000175" MajorTopicYN="N">diagnosis</QualifierName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000276" MajorTopicYN="N">immunology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D006105" MajorTopicYN="N">Granulomatous Disease, Chronic</DescriptorName><QualifierName UI="Q000175" MajorTopicYN="N">diagnosis</QualifierName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000276" MajorTopicYN="N">immunology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008297" MajorTopicYN="N">Male</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D009059" MajorTopicYN="N">Mouth Diseases</DescriptorName><QualifierName UI="Q000175" MajorTopicYN="N">diagnosis</QualifierName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000276" MajorTopicYN="Y">immunology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D009503" MajorTopicYN="N">Neutropenia</DescriptorName><QualifierName UI="Q000151" MajorTopicYN="N">congenital</QualifierName><QualifierName UI="Q000175" MajorTopicYN="N">diagnosis</QualifierName><QualifierName UI="Q000276" MajorTopicYN="N">immunology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D010214" MajorTopicYN="N">Papillon-Lefevre Disease</DescriptorName><QualifierName UI="Q000175" MajorTopicYN="N">diagnosis</QualifierName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000276" MajorTopicYN="N">immunology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D010586" MajorTopicYN="N">Phagocytes</DescriptorName><QualifierName UI="Q000276" MajorTopicYN="Y">immunology</QualifierName><QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D000081207" MajorTopicYN="N">Primary Immunodeficiency Diseases</DescriptorName><QualifierName UI="Q000175" MajorTopicYN="N">diagnosis</QualifierName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000276" MajorTopicYN="Y">immunology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D016897" MajorTopicYN="N">Respiratory Burst</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000276" MajorTopicYN="N">immunology</QualifierName></MeshHeading></MeshHeadingList><KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="Y">Dentists</Keyword><Keyword MajorTopicYN="Y">Oral presentation</Keyword><Keyword MajorTopicYN="Y">Periodontitis</Keyword><Keyword MajorTopicYN="Y">Phagocyte defects</Keyword><Keyword MajorTopicYN="Y">Primary immunodeficiency diseases</Keyword></KeywordList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="received"><Year>2021</Year><Month>05</Month><Day>14</Day></PubMedPubDate><PubMedPubDate PubStatus="revised"><Year>2021</Year><Month>07</Month><Day>10</Day></PubMedPubDate><PubMedPubDate PubStatus="accepted"><Year>2021</Year><Month>07</Month><Day>11</Day></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2021</Year><Month>7</Month><Day>17</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2021</Year><Month>9</Month><Day>18</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2021</Year><Month>7</Month><Day>16</Day><Hour>20</Hour><Minute>19</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">34271191</ArticleId><ArticleId IdType="pii">S1521-6616(21)00133-9</ArticleId><ArticleId IdType="doi">10.1016/j.clim.2021.108796</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list><country><li>Iran</li></country></list><tree><country name="Iran"><noRegion><name sortKey="Ziaei, Heliya" sort="Ziaei, Heliya" uniqKey="Ziaei H" first="Heliya" last="Ziaei">Heliya Ziaei</name></noRegion><name sortKey="Rezaei, Nima" sort="Rezaei, Nima" uniqKey="Rezaei N" first="Nima" last="Rezaei">Nima Rezaei</name><name sortKey="Shamshiri, Ahmadreza" sort="Shamshiri, Ahmadreza" uniqKey="Shamshiri A" first="Ahmadreza" last="Shamshiri">Ahmadreza Shamshiri</name><name sortKey="Tonkaboni, Arghavan" sort="Tonkaboni, Arghavan" uniqKey="Tonkaboni A" first="Arghavan" last="Tonkaboni">Arghavan Tonkaboni</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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|texte= "Oral Manifestations of Patients with Inherited Defect in Phagocyte Number or Function" a systematic review.
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