| Literature DB >> 9674901 |
B A Conrad1, R R Higgins, M E Pierpont.
Abstract
We report on a girl with duplication of 6q22.32 --> qter and microcephaly, frontal bossing, facial anomalies, and webbed neck. She has congenital heart disease, renal hypoplasia, and hearing loss along with severe developmental delay. Published reports of seven other patients are reviewed and compared. The most frequent anomalies include microcephaly, abnormal face, webbed neck, congenital heart disease, limb contractures, and developmental delay.Entities:
Mesh:
Year: 1998 PMID: 9674901 DOI: 10.1002/(sici)1096-8628(19980630)78:2<123::aid-ajmg5>3.0.co;2-p
Source DB: PubMed Journal: Am J Med Genet ISSN: 0148-7299