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Unilateral tuberous sclerosis complex
Author(s):
1. Asher Ahmed Mashhood: Department of Dermatology, Combined Military Hospital, Peshawar, Pakistan.
2. Muhamad Amjad: Department of Dermatology, Combined Military Hospital, Peshawar, Pakistan.
Abstract:
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.
Page(s): 628-630
DOI: DOI not available
Published: Journal: Journal of College of Physicians and Surgeons--Pakistan : JCPSP, Volume: 14, Issue: 10, Year: 2004
Keywords:
Unilateral Tuberous sclerosis Face Extremities Shagreen plaque Hamartoma Retinal Phacoma
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