X‐linked olivopontocerebellar atrophy

R. Lutz, J. Bodensteiner, B. Schaffer, C. Gay

Research output: Contribution to journalArticle

21 Citations (Scopus)

Abstract

We present a kindred with a relatively pure cerebellar degeneration that demonstrates X‐linked recessive inheritance. The unique clinical picture of affected patients in our kindred is characterized by an infantile onset of ataxia; very slow rate of progression; normal strength, reflexes, and sensation; and cerebellar degeneration with involvement of the olive and pons demonstrated by neuroimaging techniques. The distinction between this and other reported olivopontocerebellar degenerations is made on the basis of the clinical features and mode of inheritance. It is not clear if the distinct clinical pattern in this kindred represents variable expression of a previously reported condition, allelic variance of previously reported kindreds, or a separate clinical entity. Molecular analysis, currently underway, may help settle the issue.

Original languageEnglish (US)
Pages (from-to)417-422
Number of pages6
JournalClinical Genetics
Volume35
Issue number6
DOIs
StatePublished - Jun 1989

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Olivopontocerebellar Atrophies
Pons
Olea
Ataxia
Neuroimaging
Reflex

Keywords

  • X‐linked inheritance
  • hypotonia
  • olivopontocerebellar atrophy
  • progressive ataxia

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

X‐linked olivopontocerebellar atrophy. / Lutz, R.; Bodensteiner, J.; Schaffer, B.; Gay, C.

In: Clinical Genetics, Vol. 35, No. 6, 06.1989, p. 417-422.

Research output: Contribution to journalArticle

Lutz, R, Bodensteiner, J, Schaffer, B & Gay, C 1989, 'X‐linked olivopontocerebellar atrophy', Clinical Genetics, vol. 35, no. 6, pp. 417-422. https://doi.org/10.1111/j.1399-0004.1989.tb02966.x
Lutz, R. ; Bodensteiner, J. ; Schaffer, B. ; Gay, C. / X‐linked olivopontocerebellar atrophy. In: Clinical Genetics. 1989 ; Vol. 35, No. 6. pp. 417-422.
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