The MECP2 gene, located at Xq28, encodes methyl-CpG-binding protein 2 (MeCP2), which is frequently mutated (up to 90%) in Rett syndrome (RTT). RTT is a progressive neurodevelopmental disorder,
The purpose of the “An Analysis of the Correlation Between Poor Short-term Memory and Behavior in Children and Adolescents with Prader Willi Syndrome, 1996” was to investigate whether there were any c
Introduction:La fibrose retro-peritoneale est une maladie rare, pouvant entrainer une insuffisance renale chronique. Lobjectif de notre travail etait dapporter les caracteristiques clinico-radiologiqu
