Angelman Syndrome is a Rare Neurogenetic Disorder

Siniša Franjić

Independent Researcher, Europe

Abstract

Angelman syndrome is a genetic disorder that causes formative delays and neurological issues – challenges with discourse, adjust and strolling, and in some cases, epileptic seizures. It is caused by a transformation in chromosome 15 acquired from the mother. It is named after Dr. Harry Angelman, a British pediatrician who to begin with depicted the syndrome in 1965. Angelman syndrome is ordinarily not found until guardians start to take note formative delays when the child is between 6 and 12 months old.

Keywords: AS, Genes, Imbalances, Behavior, Health