Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleA Female with Severe Developmental Delay, Aggressive Behaviour, Hyperphagia, and Obesity: An Atypical Phenotype of a MECP2 Mutation.AuthorsBierstone, Daniel; Velsher, LeaAbstractThe article presents a case study of a female presented with aggressive behaviour, obesity, and hyperphagia, then was diagnosed with rett syndrome caused by the Methyl-CpG-Binding Protein 2 (MECP2) Mutation.SubjectsRETT syndrome; AGGRESSION (Psychology); BEHAVIOR; BIOMARKERS; DEVELOPMENTAL disabilities; FILIPINOS; GENETIC polymorphisms; MOTOR ability; GENETIC mutation; OBESITY; PHYSICAL diagnosis; PHENOTYPES; HYPERPHAGIA; DIAGNOSISPublicationUniversity of Toronto Medical Journal, 2016, Vol 94, Issue 1, p22ISSN0833-2207Publication typeCase Study