Format

Send to

Choose Destination
Hum Genet. 1996 Apr;97(4):540-2.

Congenital alacrima in a patient with G (Opitz Frias) syndrome.

Author information

1
Department of Medical Genetics, Erciyes University, Kayseri, Turkey.

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.

PMID:
8834259
[Indexed for MEDLINE]

Supplemental Content

Loading ...
Support Center