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Haploinsufficiency of the Lysine Methyltransferase 2C (KMT2C) gene results in the autosomal dominant disorder, Kleefstra syndrome 2. It is an extremely rare neurodevelopmental condition, with 14 previous reports describing varied clinical manifestations including dysmorphic features, delayed psychomotor development and delayed growth.Here, we describe a female with global developmental delay, attention deficit disorder, dyspraxia, short stature
This cross-sectional study analyzed the socio-psychological need for orthodontic treatment in children and adolescents with and without Autism Spectrum Disorder (ASD) and its association with deleterious oral habits.Children/adolescents aged 6-14 years old, with and without ASD, and their respective caregivers were included. Caregivers completed a questionnaire addressing children and adolescents' deleterious oral habits. To assess
The ongoing war in Israel, driven by Iranian-backed proxy armies, highlights critical lessons in intelligence, deterrence, AI-driven warfare, and the imperative of moral clarity that America must heed to prepare for the challenges ahead.