Tuberous sclerosis complex: A case report and literature review

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.