Literature DB >> 180264

Hereditary motor peripheral neuropathy predominantly affecting the arms.

C M Lander, M J Eadie, J H Tyrer.   

Abstract

A kinship is described in which there was slowly progressive wasting and weakness of the muscles of the upper and occasionally of the lower limbs. Some members had hyperreflexia. There were no sensory abnormalities. Electrophysiological study suggested the presence of motor peripheral polyneuropathy. The condition appeared to be inherited as an autosomal dominant. The disorder does not appear typical of any of the known hereditary polyneuropathies and it is possible that it may represent a unique hereditary, dominantly motor, polyneuropathy. The significance of the hyperreflexia is uncertain, but raises the possibility of minor central involvement as well as peripheral neuropathy.

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Mesh:

Year:  1976        PMID: 180264     DOI: 10.1016/0022-510x(76)90032-0

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


  6 in total

1.  Distal hereditary upper limb muscular atrophy.

Authors:  D W Gross; A H Rajput; M Yeung
Journal:  J Neurol Neurosurg Psychiatry       Date:  1998-02       Impact factor: 10.154

2.  A clinical, epidemiological and genetic study of hereditary motor neuropathies in Benghazi, Libya.

Authors:  K Radhakrishnan; A K Thacker; J C Maloo
Journal:  J Neurol       Date:  1988-09       Impact factor: 4.849

Review 3.  Unraveling the genetics of distal hereditary motor neuronopathies.

Authors:  Joy Irobi; Ines Dierick; Albena Jordanova; Kristl G Claeys; Peter De Jonghe; Vincent Timmerman
Journal:  Neuromolecular Med       Date:  2006       Impact factor: 3.843

4.  The distal form of spinal muscular atrophy: an unusual case demonstrating the intermediate variety.

Authors:  D A Isenberg; P A Kahn
Journal:  Postgrad Med J       Date:  1982-09       Impact factor: 2.401

5.  Linkage of the gene for an autosomal dominant form of juvenile amyotrophic lateral sclerosis to chromosome 9q34.

Authors:  P F Chance; B A Rabin; S G Ryan; Y Ding; M Scavina; B Crain; J W Griffin; D R Cornblath
Journal:  Am J Hum Genet       Date:  1998-03       Impact factor: 11.025

6.  Refinement of the Silver syndrome locus on chromosome 11q12-q14 in four families and exclusion of eight candidate genes.

Authors:  Christian Windpassinger; Klaus Wagner; Erwin Petek; Renate Fischer; Michaela Auer-Grumbach
Journal:  Hum Genet       Date:  2003-09-16       Impact factor: 4.132

  6 in total

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