| Literature DB >> 8205323 |
I W Lurie1, I V Naumchik, E A Wulfsberg.
Abstract
A family demonstrating the acrocallosal syndrome in a female proband whose sister had anencephaly is described. Two similar cases were found in the literature (Gelman-Kohan et al., 1991; Cataltepe and Tuncbilek, 1992). Analysis of the multiplex family data suggests that anencephaly may be an extreme manifestation of the spectrum of brain anomalies associated with the acrocallosal syndrome.Entities:
Mesh:
Year: 1994 PMID: 8205323
Source DB: PubMed Journal: Clin Dysmorphol ISSN: 0962-8827 Impact factor: 0.816