| Literature DB >> 14691402 |
R A Touzri1, S Goucha, L Kriaa, O Beltaif, B Fazaa, H El Andolsi, M R Kamoun, A Ouertani.
Abstract
GAPO syndrome is a rare autosomal recessive disorder whose main manifestations are: growth retardation, alopecia, pseudoanodontia and optic atrophy. We report here the ophthalmological findings in a 12-year-old Tunisian boy suffering from typical GAPO syndrome.Entities:
Mesh：
Year: 2003 PMID： 14691402
Source DB: PubMed Journal: J Fr Ophtalmol ISSN： 0181-5512 Impact factor: 0.818