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.
| Original language | English (US) |
|---|---|
| Pages (from-to) | e1-3 |
| Journal | Journal of Pediatric Ophthalmology and Strabismus |
| Volume | 47 Online |
| DOIs | |
| State | Published - 2010 |
| Externally published | Yes |
ASJC Scopus subject areas
- Pediatrics, Perinatology, and Child Health
- Ophthalmology
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