Sensory signs and symptoms in scapuloperoneal atrophy: a report of a family.

Abstract:

:A Norwegian family with asymmetrical scapuloperoneal atrophy is described. Chronic, aching shoulder pain, slight proximal and distal sensory dysfunction, and atrophy of the extensor digitorum brevis muscle occurred in some individuals. The proband had slightly impaired sensory conduction velocity, and his father exhibited impaired position sense and a vibration threshold asymmetry. EMG and muscle biopsy findings were equivocal. The syndrome is probably of neurogenic origin. It may be classified as a variant of Davidenkow's syndrome.

journal_name

Eur Neurol

journal_title

European neurology

authors

Sand T,Hestnes A

doi

10.1159/000115834

subject

Has Abstract

pub_date

1985-01-01 00:00:00

pages

405-13

issue

6

eissn

0014-3022

issn

1421-9913

journal_volume

24

pub_type

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