Literature DB >> 15456557

Unilateral tuberous sclerosis complex.

Asher Ahmed Mashhood1, Muhamad Amjad.   

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.

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Year:  2004        PMID: 15456557     DOI: 10.2004/JCPSP.628630

Source DB:  PubMed          Journal:  J Coll Physicians Surg Pak        ISSN: 1022-386X            Impact factor:   0.711


  1 in total

1.  Tuberous sclerosis--a multi system disease.

Authors:  Vijinder Arora; Inderbir Singh Nijjar; Jatinderpal Singh; P S Sandhu
Journal:  Indian J Pediatr       Date:  2008-01       Impact factor: 1.967

  1 in total

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