| Literature DB >> 6683813 |
Abstract
There are few descriptions of major neurologic dysfunctions in either the recessive or the dominant form of chondrodysplasia punctata. In the dominant trait, often called Conradi-Hünermann disease, a normal life expectancy with normal neurologic development is the usual course for those who survive the first few weeks of life. We studied an affected infant with a severe spinal cord abnormality that was present at birth and has not been reported in either recessive or dominant chondrodysplasia punctata.Entities:
Mesh:
Year: 1983 PMID: 6683813 DOI: 10.1212/wnl.33.8.1095
Source DB: PubMed Journal: Neurology ISSN: 0028-3878 Impact factor: 9.910