Yellow nail syndrome in infancy.
Identifieur interne : 004F53 ( PubMed/Curation ); précédent : 004F52; suivant : 004F54Yellow nail syndrome in infancy.
Auteurs : M. Paradisis [Australie] ; P. Van AsperenSource :
- Journal of paediatrics and child health [ 1034-4810 ] ; 1997.
Descripteurs français
- KwdFr :
- MESH :
English descriptors
- KwdEn :
- 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
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pubmed:9401896Le document en format XML
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<affiliation wicri:level="1"><nlm:affiliation>Department of Respiratory Medicine, Royal Alexandra Hospital for Children, Westmead, New South Wales, Australia.</nlm:affiliation>
<country xml:lang="fr">Australie</country>
<wicri:regionArea>Department of Respiratory Medicine, Royal Alexandra Hospital for Children, Westmead, New South Wales</wicri:regionArea>
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<author><name sortKey="Paradisis, M" sort="Paradisis, M" uniqKey="Paradisis M" first="M" last="Paradisis">M. Paradisis</name>
<affiliation wicri:level="1"><nlm:affiliation>Department of Respiratory Medicine, Royal Alexandra Hospital for Children, Westmead, New South Wales, Australia.</nlm:affiliation>
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<series><title level="j">Journal of paediatrics and child health</title>
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<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>
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<keywords scheme="KwdFr" xml:lang="fr"><term>Déficit en IgG ()</term>
<term>Déficit en IgG (sang)</term>
<term>Humains</term>
<term>Lymphoedème ()</term>
<term>Mâle</term>
<term>Nourrisson</term>
<term>Onychopathies</term>
<term>Syndrome</term>
<term>Troubles de la pigmentation</term>
<term>Épanchement pleural</term>
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<keywords scheme="MESH" qualifier="blood" xml:lang="en"><term>IgG Deficiency</term>
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<keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>IgG Deficiency</term>
<term>Lymphedema</term>
</keywords>
<keywords scheme="MESH" qualifier="sang" xml:lang="fr"><term>Déficit en IgG</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>
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<keywords scheme="MESH" xml:lang="fr"><term>Déficit en IgG</term>
<term>Humains</term>
<term>Lymphoedème</term>
<term>Mâle</term>
<term>Nourrisson</term>
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<term>Troubles de la pigmentation</term>
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<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>
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<Title>Journal of paediatrics and child health</Title>
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<ArticleTitle>Yellow nail syndrome in infancy.</ArticleTitle>
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<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>
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<MeshHeading><DescriptorName UI="D008297" MajorTopicYN="N">Male</DescriptorName>
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