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Aim and Objective: To study different imaging findings in patients presenting with tuberous sclerosis Materials &Methods: We present neuroimaging findings in three children with tuberous sclerosis showing different brain findings on MRI and ct brain scans. Result:We report the neuroimaging findings of 3 cases, two aged 12 years and one aged 2 years who clinically presented with delayed development and epilepsy with findings of subependymal giant cell astrocytoma, calcified tubers, transmantile cerebral white matter migration lines, subependymal nodules and cerebral atrophy. Conclusion: Tuberous sclerosis also known as Bourneville pringle disease is an autosomal dominant genetic disease that is characterised by the presence of multiple hamartomas in various organs. Two separate genes have been reported that have been mutated or deleted kin patients with TSC. TSC1 gene codes for the protein hamartin and TSC2 which codes for protein tuberin. Neuroimaging plays an important role in making the diagnosis of TSC as around 95% of affected patients show abnormalities in the brain.

A Three Case Series of Neuroimaging Findings of Patients with Tuberous Sclerosis Complex