| Literature DB >> 1776639 |
J Charrow1, A K Poznanski, F M Unger, M Robinow.
Abstract
We describe a brother and sister and an unrelated boy with congenital cerebellar hypoplasia and endosteal sclerosis. All 3 children presented with ataxia and developmental delay, and were found to have microcephaly, short stature, oligodontia, strabismus, nystagmus, and congenital hip dislocation. A previously published case is reviewed. The disorder appears to represent a newly recognized autosomal recessive syndrome.Entities:
Mesh:
Year: 1991 PMID: 1776639 DOI: 10.1002/ajmg.1320410417
Source DB: PubMed Journal: Am J Med Genet ISSN: 0148-7299