Case report on Tuberous Sclerosis
Vol. 2 No. 4 (2013), Case Report
Vol. 2 No. 4 (2013)

Case report on Tuberous Sclerosis

Case Report
Published 2014-12-21
Sushma Shrestha
Department of Paediatrics Kathmandu Medical College Teaching Hospital, Kathmandu
Sabina Shrestha
Department of Paediatrics Kathmandu Medical College Teaching Hospital, Kathmandu
Anil Raj Ojha
Department of Paediatrics Kathmandu Medical College Teaching Hospital, Kathmandu
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Keywords

Adenoma sebaceum
Seizure
Shagreen patch
Tuberous sclerosis

How to Cite

Shrestha, S., Shrestha, S., & Ojha, A. R. (2014). Case report on Tuberous Sclerosis. Journal of Kathmandu Medical College, 2(4), 208–210. Retrieved from https://jkmc.com.np/ojs3/index.php/journal/article/view/703
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Abstract

Tuberous Sclerosis Complex is a rare genetic disorder inherited in autosomal dominant fashion. It is a multisystem disorder involving brain, skin, kidneys, heart, eyes and lungs which becomes apparent only in late childhood, limiting the usefulness of early diagnosis in infancy. Here, we report a case of an 11 year male child with tuberous sclerosis.

DOI: http://dx.doi.org/10.3126/jkmc.v2i4.11798

Journal of Kathmandu Medical College

Vol. 2, No. 4, Issue 6, Oct.-Dec., 2013

Page : 208-210

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