Charrow J, Poznanski A K, Unger F M, Robinow M
Department of Pediatrics, Northwestern University Medical School, Chicago, Illinois.
Am J Med Genet. 1991 Dec 15;41(4):464-8. doi: 10.1002/ajmg.1320410417.
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.