Congenital yellow nail syndrome: a case report and its relationship to nonimmune fetal hydrops.
Identifieur interne : 002942 ( PubMed/Curation ); précédent : 002941; suivant : 002943Congenital yellow nail syndrome: a case report and its relationship to nonimmune fetal hydrops.
Auteurs : Arti Nanda [Koweït] ; Fahad H. Al-Essa ; Wael M. El-Shafei ; Qasem A. AlsalehSource :
- Pediatric dermatology [ 1525-1470 ]
Descripteurs français
- KwdFr :
- MESH :
- anatomopathologie : Ongles, Syndrome des ongles jaunes.
- génétique : Anasarque foeto-placentaire, Syndrome des ongles jaunes.
- Enfant d'âge préscolaire, Humains, Mâle.
English descriptors
- KwdEn :
- MESH :
- genetics : Hydrops Fetalis, Yellow Nail Syndrome.
- pathology : Nails, Yellow Nail Syndrome.
- Child, Preschool, Humans, Male.
Abstract
Yellow nail syndrome (YNS) is an uncommon disorder characterized by a triad of nail dystrophy, lymphedema, and pleural effusion. It is rare in children and congenital occurrence of YNS has been very rarely described. We report a 2-year-old Arab boy having congenital yellow nail syndrome with mild facial dysmorphism and bilateral conjunctival pigmentation born to consanguineous parents. One of his older siblings had died of nonimmune fetal hydrops (NIFH). The case supports the genetic basis of yellow nail syndrome with a possible relationship to nonimmune fetal hydrops.
DOI: 10.1111/j.1525-1470.2010.01259.x
PubMed: 20807364
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It is rare in children and congenital occurrence of YNS has been very rarely described. We report a 2-year-old Arab boy having congenital yellow nail syndrome with mild facial dysmorphism and bilateral conjunctival pigmentation born to consanguineous parents. One of his older siblings had died of nonimmune fetal hydrops (NIFH). 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