Literature DB >> 2357164

Autosomal dominant cramping disease.

K Ricker1, R T Moxley.   

Abstract

A family was studied in which four generations (16 of 41 members) suffered from painful recurrent muscle cramping. A clear pattern of autosomal dominant inheritance was noted. The cramping first developed during adolescence or early adulthood. Electromyographic analysis indicated a neurogenic origin. The cramps seemed to be due to dysfunction of the motor neurons. The mechanisms underlying this alteration are unclear and require further investigation.

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Year:  1990        PMID: 2357164     DOI: 10.1001/archneur.1990.00530070108019

Source DB:  PubMed          Journal:  Arch Neurol        ISSN: 0003-9942


  1 in total

1.  No evidence for linkage of autosomal dominant proximal spinal muscular atrophies to chromosome 5q markers.

Authors:  K Kausch; C R Müller; T Grimm; K Ricker; M Rietschel; S Rudnik-Schöneborn; K Zerres
Journal:  Hum Genet       Date:  1991-01       Impact factor: 4.132

  1 in total

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