Literature DB >> 6683813

Dominant chondrodysplasia punctata with neurologic symptoms.

R G Curless.   

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.

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Year:  1983        PMID: 6683813     DOI: 10.1212/wnl.33.8.1095

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  1 in total

1.  Progressive joint limitations as the first alarming signs in a boy with short - limbed dwarfism: A case report.

Authors:  Ali Al Kaissi; Klaus Klaushofer; Franz Grill
Journal:  Cases J       Date:  2008-08-19
  1 in total

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