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Yellow nail syndrome in infancy.

Identifieur interne : 004F53 ( PubMed/Corpus ); précédent : 004F52; suivant : 004F54

Yellow nail syndrome in infancy.

Auteurs : M. Paradisis ; P. Van Asperen

Source :

Journal of paediatrics and child health [ 1034-4810 ] ; 1997.

RBID : pubmed:9401896

English descriptors

KwdEn :
- Humans, IgG Deficiency (blood), IgG Deficiency (complications), Infant, Lymphedema (complications), Male, Nail Diseases, Pigmentation Disorders, Pleural Effusion, Syndrome.
MESH :
- blood : IgG Deficiency.
- complications : IgG Deficiency, Lymphedema.
- Humans, Infant, Male, Nail Diseases, Pigmentation Disorders, Pleural Effusion, Syndrome.

Abstract

This report describes an infant with clinical features consistent with the yellow nail syndrome (YNS), a rare autosomal dominant disorder. He presented at birth with congenital lymphoedema and was referred at 6 months of age for investigation of recurrent cough and wheeze. He had clinical and radiological evidence of bilateral pleural effusions and a pericardial effusion. Following a lung biopsy and pericardial window these were shown to be manifestations of his lymphatic abnormality. He also had persisting middle ear effusions causing conductive deafness requiring hearing aids and secondary immunodeficiency requiring regular immunoglobulin infusions.

PubMed: 9401896

Links to Exploration step

pubmed:9401896

Le document en format XML

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<author><name sortKey="Paradisis, M" sort="Paradisis, M" uniqKey="Paradisis M" first="M" last="Paradisis">M. Paradisis</name>
<affiliation><nlm:affiliation>Department of Respiratory Medicine, Royal Alexandra Hospital for Children, Westmead, New South Wales, Australia.</nlm:affiliation>
</affiliation>
</author>
<author><name sortKey="Van Asperen, P" sort="Van Asperen, P" uniqKey="Van Asperen P" first="P" last="Van Asperen">P. Van Asperen</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">PubMed</idno>
<date when="1997">1997</date>
<idno type="RBID">pubmed:9401896</idno>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">Yellow nail syndrome in infancy.</title>
<author><name sortKey="Paradisis, M" sort="Paradisis, M" uniqKey="Paradisis M" first="M" last="Paradisis">M. Paradisis</name>
<affiliation><nlm:affiliation>Department of Respiratory Medicine, Royal Alexandra Hospital for Children, Westmead, New South Wales, Australia.</nlm:affiliation>
</affiliation>
</author>
<author><name sortKey="Van Asperen, P" sort="Van Asperen, P" uniqKey="Van Asperen P" first="P" last="Van Asperen">P. Van Asperen</name>
</author>
</analytic>
<series><title level="j">Journal of paediatrics and child health</title>
<idno type="ISSN">1034-4810</idno>
<imprint><date when="1997" type="published">1997</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Humans</term>
<term>IgG Deficiency (blood)</term>
<term>IgG Deficiency (complications)</term>
<term>Infant</term>
<term>Lymphedema (complications)</term>
<term>Male</term>
<term>Nail Diseases</term>
<term>Pigmentation Disorders</term>
<term>Pleural Effusion</term>
<term>Syndrome</term>
</keywords>
<keywords scheme="MESH" qualifier="blood" xml:lang="en"><term>IgG Deficiency</term>
</keywords>
<keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>IgG Deficiency</term>
<term>Lymphedema</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Humans</term>
<term>Infant</term>
<term>Male</term>
<term>Nail Diseases</term>
<term>Pigmentation Disorders</term>
<term>Pleural Effusion</term>
<term>Syndrome</term>
</keywords>
</textClass>
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</teiHeader>
<front><div type="abstract" xml:lang="en">This report describes an infant with clinical features consistent with the yellow nail syndrome (YNS), a rare autosomal dominant disorder. He presented at birth with congenital lymphoedema and was referred at 6 months of age for investigation of recurrent cough and wheeze. He had clinical and radiological evidence of bilateral pleural effusions and a pericardial effusion. Following a lung biopsy and pericardial window these were shown to be manifestations of his lymphatic abnormality. He also had persisting middle ear effusions causing conductive deafness requiring hearing aids and secondary immunodeficiency requiring regular immunoglobulin infusions.</div>
</front>
</TEI>
<pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">9401896</PMID>
<DateCreated><Year>1998</Year>
<Month>01</Month>
<Day>22</Day>
</DateCreated>
<DateCompleted><Year>1998</Year>
<Month>01</Month>
<Day>22</Day>
</DateCompleted>
<DateRevised><Year>2007</Year>
<Month>09</Month>
<Day>24</Day>
</DateRevised>
<Article PubModel="Print"><Journal><ISSN IssnType="Print">1034-4810</ISSN>
<JournalIssue CitedMedium="Print"><Volume>33</Volume>
<Issue>5</Issue>
<PubDate><Year>1997</Year>
<Month>Oct</Month>
</PubDate>
</JournalIssue>
<Title>Journal of paediatrics and child health</Title>
<ISOAbbreviation>J Paediatr Child Health</ISOAbbreviation>
</Journal>
<ArticleTitle>Yellow nail syndrome in infancy.</ArticleTitle>
<Pagination><MedlinePgn>454-7</MedlinePgn>
</Pagination>
<Abstract><AbstractText>This report describes an infant with clinical features consistent with the yellow nail syndrome (YNS), a rare autosomal dominant disorder. He presented at birth with congenital lymphoedema and was referred at 6 months of age for investigation of recurrent cough and wheeze. He had clinical and radiological evidence of bilateral pleural effusions and a pericardial effusion. Following a lung biopsy and pericardial window these were shown to be manifestations of his lymphatic abnormality. He also had persisting middle ear effusions causing conductive deafness requiring hearing aids and secondary immunodeficiency requiring regular immunoglobulin infusions.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Paradisis</LastName>
<ForeName>M</ForeName>
<Initials>M</Initials>
<AffiliationInfo><Affiliation>Department of Respiratory Medicine, Royal Alexandra Hospital for Children, Westmead, New South Wales, Australia.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Van Asperen</LastName>
<ForeName>P</ForeName>
<Initials>P</Initials>
</Author>
</AuthorList>
<Language>eng</Language>
<PublicationTypeList><PublicationType UI="D002363">Case Reports</PublicationType>
<PublicationType UI="D016428">Journal Article</PublicationType>
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</Article>
<MedlineJournalInfo><Country>Australia</Country>
<MedlineTA>J Paediatr Child Health</MedlineTA>
<NlmUniqueID>9005421</NlmUniqueID>
<ISSNLinking>1034-4810</ISSNLinking>
</MedlineJournalInfo>
<CitationSubset>IM</CitationSubset>
<MeshHeadingList><MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D017099" MajorTopicYN="N">IgG Deficiency</DescriptorName>
<QualifierName UI="Q000097" MajorTopicYN="N">blood</QualifierName>
<QualifierName UI="Q000150" MajorTopicYN="N">complications</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D007223" MajorTopicYN="N">Infant</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008209" MajorTopicYN="Y">Lymphedema</DescriptorName>
<QualifierName UI="Q000150" MajorTopicYN="N">complications</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008297" MajorTopicYN="N">Male</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D009260" MajorTopicYN="Y">Nail Diseases</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D010859" MajorTopicYN="Y">Pigmentation Disorders</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D010996" MajorTopicYN="Y">Pleural Effusion</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D013577" MajorTopicYN="N">Syndrome</DescriptorName>
</MeshHeading>
</MeshHeadingList>
</MedlineCitation>
<PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>1997</Year>
<Month>12</Month>
<Day>24</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="medline"><Year>1997</Year>
<Month>12</Month>
<Day>24</Day>
<Hour>0</Hour>
<Minute>1</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="entrez"><Year>1997</Year>
<Month>12</Month>
<Day>24</Day>
<Hour>0</Hour>
<Minute>0</Minute>
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</History>
<PublicationStatus>ppublish</PublicationStatus>
<ArticleIdList><ArticleId IdType="pubmed">9401896</ArticleId>
</ArticleIdList>
</PubmedData>
</pubmed>
</record>

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Yellow nail syndrome in infancy.

Yellow nail syndrome in infancy.

Source :

English descriptors

Abstract

Links to Exploration step

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri

Pour générer des pages wiki