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.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.3928/01913913-20100920-06 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!