
Tuberous sclerosis with oral manifestations: A rare case report
Author(s) -
Sps Sodhi,
Ramandeep Singh Dang,
Gursimrat Kaur Brar
Publication year - 2016
Publication title -
international journal of applied and basic medical research/international journal of applied and basic medical research
Language(s) - English
Resource type - Journals
eISSN - 2248-9606
pISSN - 2229-516X
DOI - 10.4103/2229-516x.174018
Subject(s) - tuberous sclerosis , incidence (geometry) , dermatology , medicine , epilepsy , pediatrics , trait , family history , pathology , psychiatry , surgery , physics , computer science , optics , programming language
Tuberous sclerosis complex (TSC) is a neurocutaneous syndrome, inherited as an autosomal dominant trait with a high incidence of sporadic cases and protean clinical expression, with a incidence of prevalence between 1 in 10,000 and 1 in 170,000. The cardinal features of TSC are skin lesions, convulsive seizures, and mental retardation. We report a sporadically occurring case of definite TSC in a young female who presented with oral and cutaneous manifestations without mental retardation or history of convulsive seizures, which to the best of our knowledge has not been reported so far.