Article
CHD7 mutations and CHARGE syndrome: the clinical implications of an expanding phenotype.
Journal of medical genetics - 1 May 2011
Bergman J E H, Janssen N, Hoefsloot L H, Jongmans M C J, Hofstra R M W, van Ravenswaaij-Arts C M A
Abstract excerpt
BACKGROUND: CHARGE syndrome is a highly variable, multiple congenital anomaly syndrome, of which the complete phenotypic spectrum was only revealed after identification of the causative gene in 2004. CHARGE is an acronym for ocular coloboma, congenital heart defects, choanal atresia, retardation of growth and development, genital hypoplasia, and ear anomalies associated with deafness. This typical combination of...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
