Retinal detachment in median cleft-face syndrome.

AUTOR(ES)

Feiler-Ofry, V

RESUMO

A 7-year-old boy had an unusual association of median cleft-face syndrome, a characteristic physiognomy, unilateral retinal dysplasia, and bilateral retinal detachment. Despite surgical treatment to both eyes he became blind. The hereditary pattern operating in this complex disorder was found to be consistent with an autosomal dominant trait.

Documentos Relacionados

• Retinal detachment in Axenfeld-Rieger syndrome.
• Surgical management of retinal detachment associated with the acute retinal necrosis syndrome.
• Acute retinal necrosis syndrome.
• Median--ulnar nerve communications and carpal tunnel syndrome.
• Retinal pathology in the Kearns-Sayre syndrome.