1.
J Pediatr Ophthalmol Strabismus
; 45(6): 366-7, 2008.
Artigo
em Inglês
| MEDLINE
| ID: mdl-19043949
RESUMO
Hirschsprung disease, bilateral retinoblastoma, and craniofacial dysmorphism with an interstitial deletion of chromosome 13 is a rare gene deletion syndrome that has twice before been described in white children. The authors present the third report of such a case in a South African child of Indian-Asian descent.