Adult-onset autosomal recessive neurogenic scapuloperoneal syndrome

R. Tandan, Ashok Verma, M. Mohire

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

We report a brother and sister who showed weakness, atrophy and fasciculations starting in adulthood, predominantly affecting the muscles of the shoulder girdles and distal lower extremities. Mild ptosis and facial weakness were present in both. Electrophysiological studies and muscle histology supported a neurogenic basis for the autosomal recessive scapuloperoneal syndrome in this sibship.

Original languageEnglish
Pages (from-to)201-209
Number of pages9
JournalJournal of the Neurological Sciences
Volume94
Issue number1-3
DOIs
StatePublished - Jan 1 1989
Externally publishedYes

Fingerprint

Fasciculation
Muscles
Atrophy
Lower Extremity
Histology

Keywords

  • Adult-onset
  • Autosomal recessive
  • Neurogenic
  • Scapuloperoneal syndrome

ASJC Scopus subject areas

  • Aging
  • Clinical Neurology
  • Surgery
  • Neuroscience(all)
  • Developmental Neuroscience
  • Neurology

Cite this

Adult-onset autosomal recessive neurogenic scapuloperoneal syndrome. / Tandan, R.; Verma, Ashok; Mohire, M.

In: Journal of the Neurological Sciences, Vol. 94, No. 1-3, 01.01.1989, p. 201-209.

Research output: Contribution to journalArticle

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