| Literature DB >> 22156792 |
Brahim Tabarki1, Shatha Al Shafi, Nawal Al Adwani, Saad Al Shahwan.
Abstract
A rare sex chromosome aneuploidy syndrome, 49,XXXXY syndrome is characterized by mental retardation with severe learning difficulties, craniofacial and skeletal abnormalities, hypogonadism, and congenital heart disease. The authors describe a 30-month-old boy with 49,XXXXY syndrome, global developmental delay and white matter changes in the brain magnetic resonance imaging. They reviewed the literature to delineate a specific magnetic resonance imaging pattern of 49,XXXXY syndrome.Entities:
Mesh:
Year: 2011 PMID: 22156792 DOI: 10.1177/0883073811424797
Source DB: PubMed Journal: J Child Neurol ISSN: 0883-0738 Impact factor: 1.987