| Literature DB >> 8074149 |
A G Krishna1, E M Scrimgeour, T H Zawawi.
Abstract
We studied a 28-year-old Yemeni woman with typical Seckel syndrome. Two deceased sibs, a twin sister and a brother, had also been affected. The father of these individuals was married to his cousin's daughter: the pedigree suggests autosomal recessive inheritance. Classical Seckel syndrome has not been reported previously in Arabs, and this appears to be the first report from the Middle East.Entities:
Mesh:
Year: 1994 PMID: 8074149 DOI: 10.1002/ajmg.1320510310
Source DB: PubMed Journal: Am J Med Genet ISSN: 0148-7299