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J West Afr Coll Surg ; 12(4): 126-129, 2022.
Artículo en Inglés | MEDLINE | ID: mdl-36590774

RESUMEN

Alport syndrome is an inherited disease with a trio of hearing loss, ocular abnormalities, and progressive renal failure. The most severe form is commonest in males due to the X-linked mutations. We present a 25-year-old male who presented with deterioration of vision over 5 years, further questioning revealed use of hearing aid. Although he had no renal-related complaints, investigation revealed proteinuria. There is a need for proper examination of developmental cataract to avoid missing out on Alport syndrome.

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