1.
Hum Genet
; 97(4): 540-2, 1996 Apr.
Article
in English
| MEDLINE
| ID: mdl-8834259
ABSTRACT
Congenital alacrima is an autosomal dominant disorder showing markedly deficient lacrimation and punctate corneal epithelial erosions. The G (Opitz-Frias) syndrome is also an autosomal dominant disorder characterised by hypertelorism, hypospadias, stridor, and dysphagia. Here we report a 5-year-old boy with the G syndrome presenting congenital alacrima.