Authors : Amjad Ali, Dipankar Das, Harsha Bhattacharjee, Damaris Magdalene, Divakant Misra
DOI : 10.18231/2395-1451.2018.0065
Volume : 4
Issue : 3
Year : 0
Page No : 290-293
Tuberous Sclerosis Complex is a rare genetic disorder of autosomal dominant inheritance. It is a neurocutaneous syndrome exhibiting multiple hamartomatous proliferations involving multiple organ system such as brain, kidney, heart, lungs, eyes and skin. Here, we present a case report of a 7year old male patient with characteristic clinical and radiological features of Tuberosis Sclerosis Complex.
Keywords: Genetic disorder, Multiple hamartomas, Neurocutaneous syndrome, Tuberous sclerosis complex.