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J Coll Physicians Surg Pak ; 14(10): 628-30, 2004 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-15456557

RESUMO

Tuberous sclerosis is a rare genetic disease of autosomal dominant inheritance, associated with hamartomata formation in several organs and various skin findings. A case of young male is presented here with multiple fibromas on right side of his face, peri-ungual fibromas in right index and middle fingers and right second toe, a small shagreen plaque over right lower back and multiple, ill-defined hypopigmented patches over his right side of the trunk and right buttocks. Fundoscopic examination revealed retinal phacomas on right side. CT-scan brain showed right-sided paraventricular calcification.


Assuntos
Esclerose Tuberosa/diagnóstico , Adulto , Humanos , Masculino , Esclerose Tuberosa/terapia
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