| Literature DB >> 9450876 |
S G Frints1, E F Schoenmakers, E Smeets, P Petit, J P Fryns.
Abstract
We report on a de novo 7q36 deletion in a 3-month-old girl with manifestations of the 7q terminal deletion syndrome. Only minimal findings of holoprosencephaly (HPE) were present since only a partial corpus callosum hypoplasia was seen on a magnetic resonance imaging scan of the brain. Extensive fluorescence in situ hybridization analysis showed that the HPE3 critical gene region, inclusive Sonic hedgehog (SHH), En2 (HOX1), and HTR5A, was deleted. A review of 33 other patients with a de novo terminal 7q deletion and the different types of HPE manifestations within these patients will be presented.Entities:
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Year: 1998 PMID: 9450876 DOI: 10.1002/(sici)1096-8628(19980113)75:2<153::aid-ajmg6>3.0.co;2-u
Source DB: PubMed Journal: Am J Med Genet ISSN: 0148-7299