772
The journal Orvosi Hetilap has published an article about tuberous sclerosis complex. Tuberous sclerosis complex is a rare disease with high phenotypic heterogeneity, characterized by the appearance of multiplex hamartomas in the different organs. The disease is inherited by autosomal dominant manner, due to the mutations of two genes: the TSC1 or the TSC2. The full-text article you can find here.