Yellow nail syndrome: not a genetic disorder? Eleven new cases and a review of the literature.
Identifieur interne : 002676 ( Ncbi/Merge ); précédent : 002675; suivant : 002677Yellow nail syndrome: not a genetic disorder? Eleven new cases and a review of the literature.
Auteurs : S R Hoque [Royaume-Uni] ; S. Mansour ; Peter Mortimer (dermatologue) [Royaume-Uni]Source :
- The British journal of dermatology [ 0007-0963 ] ; 2007.
Descripteurs français
- KwdFr :
- Adulte, Adulte d'âge moyen, Femelle, Humains, Lymphoedème (anatomopathologie), Lymphoedème (génétique), Mâle, Onychopathies (anatomopathologie), Onychopathies (génétique), Pedigree, Sujet âgé, Sujet âgé de 80 ans ou plus, Syndrome, Système lymphatique (physiopathologie), Troubles de la pigmentation (anatomopathologie), Troubles de la pigmentation (génétique), Études rétrospectives.
- MESH :
- anatomopathologie : Lymphoedème, Onychopathies, Troubles de la pigmentation.
- génétique : Lymphoedème, Onychopathies, Troubles de la pigmentation.
- physiopathologie : Système lymphatique.
- Adulte, Adulte d'âge moyen, Femelle, Humains, Mâle, Pedigree, Sujet âgé, Sujet âgé de 80 ans ou plus, Syndrome, Études rétrospectives.
English descriptors
- KwdEn :
- Adult, Aged, Aged, 80 and over, Female, Humans, Lymphatic System (physiopathology), Lymphedema (genetics), Lymphedema (pathology), Male, Middle Aged, Nail Diseases (genetics), Nail Diseases (pathology), Pedigree, Pigmentation Disorders (genetics), Pigmentation Disorders (pathology), Retrospective Studies, Syndrome.
- MESH :
- genetics : Lymphedema, Nail Diseases, Pigmentation Disorders.
- pathology : Lymphedema, Nail Diseases, Pigmentation Disorders.
- physiopathology : Lymphatic System.
- Adult, Aged, Aged, 80 and over, Female, Humans, Male, Middle Aged, Pedigree, Retrospective Studies, Syndrome.
Abstract
Yellow nail syndrome (YNS) is characterized by the triad of characteristic nail changes, chronic respiratory disorders and primary lymphoedema. Over 100 cases have been published, most of which have been sporadic. Despite this, YNS is classified as a dominantly inherited lymphoedema with variable expression. There have been only a few published reports where a positive family history (FH) has been documented in cases of YNS.
DOI: 10.1111/j.1365-2133.2007.07894.x
PubMed: 17459037
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Mansour</name></author><author><name sortKey="Mortimer, P S" sort="Mortimer, P S" uniqKey="Mortimer P" first="P S" last="Mortimer">Peter Mortimer (dermatologue)</name><affiliation><country>Royaume-Uni</country><placeName><settlement type="city">Londres</settlement><region type="country">Angleterre</region><region type="région" nuts="1">Grand Londres</region></placeName><orgName type="university">Université de Londres</orgName></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2007">2007</date><idno type="RBID">pubmed:17459037</idno><idno type="pmid">17459037</idno><idno type="doi">10.1111/j.1365-2133.2007.07894.x</idno><idno type="wicri:Area/PubMed/Corpus">003682</idno><idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">003682</idno><idno type="wicri:Area/PubMed/Curation">003682</idno><idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Curation">003682</idno><idno type="wicri:Area/PubMed/Checkpoint">003682</idno><idno type="wicri:explorRef" wicri:stream="Checkpoint" wicri:step="PubMed">003682</idno><idno type="wicri:Area/Ncbi/Merge">002676</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Yellow nail syndrome: not a genetic disorder? Eleven new cases and a review of the literature.</title><author><name sortKey="Hoque, S R" sort="Hoque, S R" uniqKey="Hoque S" first="S R" last="Hoque">S R Hoque</name><affiliation wicri:level="1"><nlm:affiliation>Department of Dermatology, St Helier Hospital, Carshalton, Surrey, UK. Shamali.Hoque@epsom-sthelier.nhs.uk</nlm:affiliation><country xml:lang="fr">Royaume-Uni</country><wicri:regionArea>Department of Dermatology, St Helier Hospital, Carshalton, Surrey</wicri:regionArea><wicri:noRegion>Surrey</wicri:noRegion></affiliation></author><author><name sortKey="Mansour, S" sort="Mansour, S" uniqKey="Mansour S" first="S" last="Mansour">S. Mansour</name></author><author><name sortKey="Mortimer, P S" sort="Mortimer, P S" uniqKey="Mortimer P" first="P S" last="Mortimer">Peter Mortimer (dermatologue)</name><affiliation><country>Royaume-Uni</country><placeName><settlement type="city">Londres</settlement><region type="country">Angleterre</region><region type="région" nuts="1">Grand Londres</region></placeName><orgName type="university">Université de Londres</orgName></affiliation></author></analytic><series><title level="j">The British journal of dermatology</title><idno type="ISSN">0007-0963</idno><imprint><date when="2007" type="published">2007</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adult</term><term>Aged</term><term>Aged, 80 and over</term><term>Female</term><term>Humans</term><term>Lymphatic System (physiopathology)</term><term>Lymphedema (genetics)</term><term>Lymphedema (pathology)</term><term>Male</term><term>Middle Aged</term><term>Nail Diseases (genetics)</term><term>Nail Diseases (pathology)</term><term>Pedigree</term><term>Pigmentation Disorders (genetics)</term><term>Pigmentation Disorders (pathology)</term><term>Retrospective Studies</term><term>Syndrome</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Adulte</term><term>Adulte d'âge moyen</term><term>Femelle</term><term>Humains</term><term>Lymphoedème (anatomopathologie)</term><term>Lymphoedème (génétique)</term><term>Mâle</term><term>Onychopathies (anatomopathologie)</term><term>Onychopathies (génétique)</term><term>Pedigree</term><term>Sujet âgé</term><term>Sujet âgé de 80 ans ou plus</term><term>Syndrome</term><term>Système lymphatique (physiopathologie)</term><term>Troubles de la pigmentation (anatomopathologie)</term><term>Troubles de la pigmentation (génétique)</term><term>Études rétrospectives</term></keywords><keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr"><term>Lymphoedème</term><term>Onychopathies</term><term>Troubles de la pigmentation</term></keywords><keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Lymphedema</term><term>Nail Diseases</term><term>Pigmentation Disorders</term></keywords><keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Lymphoedème</term><term>Onychopathies</term><term>Troubles de la pigmentation</term></keywords><keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Lymphedema</term><term>Nail Diseases</term><term>Pigmentation Disorders</term></keywords><keywords scheme="MESH" qualifier="physiopathologie" xml:lang="fr"><term>Système lymphatique</term></keywords><keywords scheme="MESH" qualifier="physiopathology" xml:lang="en"><term>Lymphatic System</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Adult</term><term>Aged</term><term>Aged, 80 and over</term><term>Female</term><term>Humans</term><term>Male</term><term>Middle Aged</term><term>Pedigree</term><term>Retrospective Studies</term><term>Syndrome</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Adulte</term><term>Adulte d'âge moyen</term><term>Femelle</term><term>Humains</term><term>Mâle</term><term>Pedigree</term><term>Sujet âgé</term><term>Sujet âgé de 80 ans ou plus</term><term>Syndrome</term><term>Études rétrospectives</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Yellow nail syndrome (YNS) is characterized by the triad of characteristic nail changes, chronic respiratory disorders and primary lymphoedema. Over 100 cases have been published, most of which have been sporadic. Despite this, YNS is classified as a dominantly inherited lymphoedema with variable expression. There have been only a few published reports where a positive family history (FH) has been documented in cases of YNS.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">17459037</PMID><DateCreated><Year>2007</Year><Month>05</Month><Day>30</Day></DateCreated><DateCompleted><Year>2007</Year><Month>09</Month><Day>06</Day></DateCompleted><DateRevised><Year>2007</Year><Month>05</Month><Day>30</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Print">0007-0963</ISSN><JournalIssue CitedMedium="Print"><Volume>156</Volume><Issue>6</Issue><PubDate><Year>2007</Year><Month>Jun</Month></PubDate></JournalIssue><Title>The British journal of dermatology</Title><ISOAbbreviation>Br. J. Dermatol.</ISOAbbreviation></Journal><ArticleTitle>Yellow nail syndrome: not a genetic disorder? Eleven new cases and a review of the literature.</ArticleTitle><Pagination><MedlinePgn>1230-4</MedlinePgn></Pagination><Abstract><AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Yellow nail syndrome (YNS) is characterized by the triad of characteristic nail changes, chronic respiratory disorders and primary lymphoedema. Over 100 cases have been published, most of which have been sporadic. Despite this, YNS is classified as a dominantly inherited lymphoedema with variable expression. There have been only a few published reports where a positive family history (FH) has been documented in cases of YNS.</AbstractText><AbstractText Label="OBJECTIVES" NlmCategory="OBJECTIVE">To conduct a retrospective survey investigating the genetic basis of YNS.</AbstractText><AbstractText Label="METHODS" NlmCategory="METHODS">The notes of 11 patients diagnosed with YNS were examined for documentation of a positive FH, and in addition a postal questionnaire was sent to these patients.</AbstractText><AbstractText Label="RESULTS" NlmCategory="RESULTS">Only one of the 11 patients had a relevant FH. In addition, four patients had complete recovery of their nail changes.</AbstractText><AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">This is the first retrospective study of YNS to document clear remission of nail changes. The lack of a positive FH in the majority of patients in our study, the late onset of the disease and recovery of nail changes in our patients suggest that YNS may not be primarily a genetic disease as it is currently classified.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Hoque</LastName><ForeName>S R</ForeName><Initials>SR</Initials><AffiliationInfo><Affiliation>Department of Dermatology, St Helier Hospital, Carshalton, Surrey, UK. Shamali.Hoque@epsom-sthelier.nhs.uk</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Mansour</LastName><ForeName>S</ForeName><Initials>S</Initials></Author><Author ValidYN="Y"><LastName>Mortimer</LastName><ForeName>P S</ForeName><Initials>PS</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D016454">Review</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2007</Year><Month>04</Month><Day>25</Day></ArticleDate></Article><MedlineJournalInfo><Country>England</Country><MedlineTA>Br J Dermatol</MedlineTA><NlmUniqueID>0004041</NlmUniqueID><ISSNLinking>0007-0963</ISSNLinking></MedlineJournalInfo><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D000328" MajorTopicYN="N">Adult</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D000368" MajorTopicYN="N">Aged</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D000369" MajorTopicYN="N">Aged, 80 and over</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008208" MajorTopicYN="N">Lymphatic System</DescriptorName><QualifierName UI="Q000503" MajorTopicYN="N">physiopathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008209" MajorTopicYN="N">Lymphedema</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName><QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008297" MajorTopicYN="N">Male</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008875" MajorTopicYN="N">Middle Aged</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D009260" MajorTopicYN="N">Nail Diseases</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName><QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D010375" MajorTopicYN="N">Pedigree</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D010859" MajorTopicYN="N">Pigmentation Disorders</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName><QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D012189" MajorTopicYN="N">Retrospective Studies</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D013577" MajorTopicYN="N">Syndrome</DescriptorName></MeshHeading></MeshHeadingList><NumberOfReferences>24</NumberOfReferences></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>2007</Year><Month>4</Month><Day>27</Day><Hour>9</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2007</Year><Month>9</Month><Day>7</Day><Hour>9</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2007</Year><Month>4</Month><Day>27</Day><Hour>9</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">17459037</ArticleId><ArticleId IdType="pii">BJD7894</ArticleId><ArticleId IdType="doi">10.1111/j.1365-2133.2007.07894.x</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list><country><li>Royaume-Uni</li></country><region><li>Angleterre</li><li>Grand Londres</li></region><settlement><li>Londres</li></settlement><orgName><li>Université de Londres</li></orgName></list><tree><noCountry><name sortKey="Mansour, S" sort="Mansour, S" uniqKey="Mansour S" first="S" last="Mansour">S. Mansour</name></noCountry><country name="Royaume-Uni"><noRegion><name sortKey="Hoque, S R" sort="Hoque, S R" uniqKey="Hoque S" first="S R" last="Hoque">S R Hoque</name></noRegion><name sortKey="Mortimer, P S" sort="Mortimer, P S" uniqKey="Mortimer P" first="P S" last="Mortimer">Peter Mortimer (dermatologue)</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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