Article
Genetic disorders associated with postnatal microcephaly.
American journal of medical genetics. Part C, Seminars in medical genetics - 1 Jun 2014
Seltzer Laurie E, Paciorkowski Alex R
Abstract excerpt
Several genetic disorders are characterized by normal head size at birth, followed by deceleration in head growth resulting in postnatal microcephaly. Among these are classic disorders such as Angelman syndrome and MECP2-related disorder (formerly Rett syndrome), as well as more recently described clinical entities associated with mutations in CASK, CDKL5, CREBBP, and EP300 (Rubinstein-Taybi syndrome), FOXG1,...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
