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. 1988 Oct;63(10):1260–1261. doi: 10.1136/adc.63.10.1260

Ataxic cerebral palsy and genetic predisposition.

G Miller 1
PMCID: PMC1779014  PMID: 3196054

Abstract

It was calculated that in the 962 family members of 36 patients with ataxic cerebral palsy there were 75 (8%) with a history of neurodevelopmental disorder and 31 (3%) with a major congenital malformation. This was not significantly greater than expected, and does not support the hypothesis of a genetic non-Mendelian role in the aetiology of ataxic cerebral palsy.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. BAX M. C. TERMINOLOGY AND CLASSIFICATION OF CEREBRAL PALSY. Dev Med Child Neurol. 1964 Jun;6:295–297. doi: 10.1111/j.1469-8749.1964.tb10791.x. [DOI] [PubMed] [Google Scholar]
  2. Hagberg G., Hagberg G., Olow I. The changing panorama of cerebral palsy in Sweden 1954-1970. II. Analysis of the various syndromes. Acta Paediatr Scand. 1975 Mar;64(2):193–200. doi: 10.1111/j.1651-2227.1975.tb03821.x. [DOI] [PubMed] [Google Scholar]
  3. Monreal F. J. Consideration of genetic factors in cerebral palsy. Dev Med Child Neurol. 1985 Jun;27(3):325–330. doi: 10.1111/j.1469-8749.1985.tb04543.x. [DOI] [PubMed] [Google Scholar]

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