Blepharophimosis Syndrome with Retinitis Pigmentosa (RP) A Rare Syndrome Complex

Journal Title: Journal of Medical Science And clinical Research - Year 2017, Vol 5, Issue 1

Abstract

telecanthus (an abnormally wide intracanthal distance with normal interpupillary distance), epicanthus inversus (skin fold arising from the lower eyelid that covers the medial canthus) and blepharophimosis (profound narrowing of the palpebral fissure). Retinitis pigmentosa (RP) are a group of inherited disorders of the retina that are characterized by progressive dysfunction involving photoreceptors leading to eventual atrophy of several retinal layers .We report a patient with RP associated with blepharophimosis. We could find only one case of such features reported earlier.

Authors and Affiliations

Sumera Zargar

Keywords

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  • EP ID EP246297
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How To Cite

Sumera Zargar (2017). Blepharophimosis Syndrome with Retinitis Pigmentosa (RP) A Rare Syndrome Complex. Journal of Medical Science And clinical Research, 5(1), 15559-15561. https://europub.co.uk/articles/-A-246297