| Literature DB >> 24862881 |
Judith M A Verhagen1, Wilma Oostdijk2, Cecilia E J Terwisscha van Scheltinga3, Nicoline E Schalij-Delfos4, Yolande van Bever5.
Abstract
Kabuki syndrome is a rare genetic disorder characterized by intellectual disability and multiple congenital anomalies, including short stature, peculiar facial appearance, skeletal anomalies, a variety of visceral malformations and abnormal dermatoglyphic patterns. We describe a case of Kabuki syndrome presenting with atypical features, consisting of bilateral microphthalmia, coloboma, anal atresia and panhypopituitarism, showing considerable phenotypic overlap with CHARGE syndrome. This report demonstrates that clinical follow-up and molecular genetic testing can be useful for establishing the correct diagnosis.Entities:
Keywords: Anal atresia; Coloboma; Kabuki syndrome; Microphthalmia; Panhypopituitarism
Mesh:
Year: 2014 PMID: 24862881 DOI: 10.1016/j.ejmg.2014.05.005
Source DB: PubMed Journal: Eur J Med Genet ISSN: 1769-7212 Impact factor: 2.708