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Indian J Ophthalmol ; 2008 Sep-Oct; 56(5): 430-4
Article in English | IMSEAR | ID: sea-70796

ABSTRACT

We present a two-generation family with Brown syndrome. The proband was a six and a half-year-old female who presented with a history of failure of dextro-elevation of her left eye. A full ophthalmic evaluation was consistent with a left Brown syndrome. Family history revealed that her mother was operated on as a child for left Brown syndrome and examination of her four and a half-year-old sibling showed similar affection in the left eye. Autosomal dominant inheritance has been postulated in this condition. To our knowledge this is the first report of three members of a two-generation family with left-sided Brown syndrome. Genetic counseling of Brown syndrome cases is advised; nevertheless, identification of the responsible gene should shed more light on its genetics.


Subject(s)
Adult , Child , Eye Movements/physiology , Female , Follow-Up Studies , Genetic Predisposition to Disease , Humans , Infant , Male , Nuclear Family , Ocular Motility Disorders/genetics , Pedigree , Phenotype , Vision, Binocular
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