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Review Case Reports
[Ocular manifestation in GAPO syndrome. Report of the first tunisian case].
- R A Touzri, S Goucha, L Kriaa, O Beltaif, B Fazaa, H El Andolsi, M R Kamoun, and A Ouertani.
- Service d'Ophtalmologie, Hôpital Universitaire de Charles Nicolle, Tunis, Tunisie. fr.touzri@gnet.tn
- J Fr Ophtalmol. 2003 Dec 1; 26 (10): 1067-70.
AbstractGAPO 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.
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