ABSTRACT
We report a male, Qatari infant, born in September 2001 at Hamad Medical Corporation [Doha, Qatar] with bilateral, asymmetric cryptophthalmos. Parents presented first degree familial consanguinity, but negative for ocular abnormalities. General physical examination was unremarkable. Ocular exam showed incomplete variety in the right eye and complete on the left eye. Partially exposed right eye exhibited total corneal opacity. The left eye B Scan Ocular Ultrasound depicted anterior megalophthalmos and enlargement of globe's axial length. CT Scan revealed anterior chamber dysgenesis in the right eye, with normal posterior segment. Cryptophthalmos is a very rare inherited condition, mainly when it appears as an isolated case and not syndromic. To our knowledge, this is the first isolated non syndromic cryptopthalmos case reported in Qatar and in the Gulf countries
ABSTRACT
To evaluate the results of the treatment of Retinopathy of Prematurity [ROP] patients in Qatar a retrospective analysis was made of 43 infants treated between January 1999 and December 2002 initially with indirect laser transpupillary photocoagulation. Cryotherapy was used only on those needing re-treatment. A favorable outcome overall was obtained in 40 cases [90%] after ten received re-treatment. The statistical interpretation, complicating factors and outcomes are discussed. It is concluded that the results of threshold ROP treatment in Qatar are encouraging