| Literature DB >> 20807364 |
Arti Nanda1, Fahad H Al-Essa, Wael M El-Shafei, Qasem A Alsaleh.
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.Entities:
Mesh:
Year: 2010 PMID: 20807364 DOI: 10.1111/j.1525-1470.2010.01259.x
Source DB: PubMed Journal: Pediatr Dermatol ISSN: 0736-8046 Impact factor: 1.588