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  • Title: [Ocular manifestation in GAPO syndrome. Report of the first tunisian case].
    Author: Touzri RA, Goucha S, Kriaa L, Beltaif O, Fazaa B, El Andolsi H, Kamoun MR, Ouertani A.
    Journal: J Fr Ophtalmol; 2003 Dec; 26(10):1067-70. PubMed ID: 14691402.
    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.
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