Case Report on Tuberous sclerosis

Abstract

Tuberous sclerosis is a rare genetic disorder inherited in a autosomal dominant fashion. It is a multisystem disoder involving brain, skin, kidneys, heart, eyes, and lungs which become apparent only in late childhood, limiting the usefulness of early diagnosis in infancy.[1] It is characterised by cutaneous changes , neurologic condition, and formation of hamartomas in multiple organs leading to morbidity and mortality. Here we present a case report of a 21 year old male patient presenting with seizure diagnosed as a case of tuberous sclerosis.