| Literature DB >> 20886807 |
Robert M Knape1, Kunjal B Gandhi, Sanjeev Y Tuli, Nausheen Khuddus.
Abstract
Congenital hemidysplasia with ichthyosiform erythroderma and limb defects (CHILD) syndrome is a rare disorder characterized by birth defects of several organ systems, including the skin, viscera, musculoskeletal system, and central nervous system. The authors present the first report of CHILD syndrome with ocular manifestations in a patient with progressive bilateral optic nerve atrophy. Copyright 2010, SLACK Incorporated.Entities:
Mesh:
Year: 2010 PMID: 20886807 DOI: 10.3928/01913913-20100920-06
Source DB: PubMed Journal: J Pediatr Ophthalmol Strabismus ISSN: 0191-3913 Impact factor: 1.402