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[Hereditary motor sensory neuropathies].
Fortschr Neurol Psychiatr. 1982 Nov; 50(11):349-65.FN

Abstract

The descriptive term "hereditary motor sensory neuropathy (HMSN)" includes a group of disorders of different nosology which besides heredity show a progressive distal symmetrical motor sensory neuropathy as a common clinical feature. The etiology of these disorders is probably different. According to electrophysiological and morphological findings two major types of HMSN can be distinguished from each other: 1. The neural type (HMSN, type I) is characterized by axonal degeneration, segmental demyelination and hypertrophic changes. The nerve conduction velocity in this type is significantly slowed. 2. The neuronal type (HMSN, type II) shows axonal degeneration with secondary segmental demyelination and no hypertrophic nerve changes. The nerve conduction velocity in these cases is normal or insignificantly decreased. This paper includes a historical review and a detailed description of the clinical, electrophysiological and morphological findings of the two major types of HMSN. The current classifications of HMSN are cited and critically discussed.

Authors

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Pub Type(s)

English Abstract
Journal Article

Language

ger

PubMed ID

6185402

Citation

Meier, C, and W Tackmann. "[Hereditary Motor Sensory Neuropathies]." Fortschritte Der Neurologie-Psychiatrie, vol. 50, no. 11, 1982, pp. 349-65.
Meier C, Tackmann W. [Hereditary motor sensory neuropathies]. Fortschr Neurol Psychiatr. 1982;50(11):349-65.
Meier, C., & Tackmann, W. (1982). [Hereditary motor sensory neuropathies]. Fortschritte Der Neurologie-Psychiatrie, 50(11), 349-65.
Meier C, Tackmann W. [Hereditary Motor Sensory Neuropathies]. Fortschr Neurol Psychiatr. 1982;50(11):349-65. PubMed PMID: 6185402.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - [Hereditary motor sensory neuropathies]. AU - Meier,C, AU - Tackmann,W, PY - 1982/11/1/pubmed PY - 1982/11/1/medline PY - 1982/11/1/entrez SP - 349 EP - 65 JF - Fortschritte der Neurologie-Psychiatrie JO - Fortschr Neurol Psychiatr VL - 50 IS - 11 N2 - The descriptive term "hereditary motor sensory neuropathy (HMSN)" includes a group of disorders of different nosology which besides heredity show a progressive distal symmetrical motor sensory neuropathy as a common clinical feature. The etiology of these disorders is probably different. According to electrophysiological and morphological findings two major types of HMSN can be distinguished from each other: 1. The neural type (HMSN, type I) is characterized by axonal degeneration, segmental demyelination and hypertrophic changes. The nerve conduction velocity in this type is significantly slowed. 2. The neuronal type (HMSN, type II) shows axonal degeneration with secondary segmental demyelination and no hypertrophic nerve changes. The nerve conduction velocity in these cases is normal or insignificantly decreased. This paper includes a historical review and a detailed description of the clinical, electrophysiological and morphological findings of the two major types of HMSN. The current classifications of HMSN are cited and critically discussed. SN - 0720-4299 UR - https://www.unboundmedicine.com/medline/citation/6185402/[Hereditary_motor_sensory_neuropathies]_ L2 - http://www.thieme-connect.com/DOI/DOI?10.1055/s-2007-1002277 DB - PRIME DP - Unbound Medicine ER -