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[Heterogeneity of neural muscular atrophies].
Nervenarzt. 1986 Jul; 57(7):419-21.N

Abstract

Classification of the hereditary motor and sensory neuropathies is discussed and findings reported in the recent literature are compared to our own findings in a kinship with autosomal dominant CMT. Previous studies in CMT-families with comparable slow nerve conduction velocities had shown positive linkage of this hereditary neuropathy to the Duffy blood group locus; however, blood group typing in the recently studied kinship excluded close linkage, which may indicate the existence of another sub-group in this entity. Testing of visually evoked potentials in this kindred demonstrated significant differences in P 100 latencies of the families of twin brothers. This intrafamilial difference may also be an expression of heterogeneity.

Authors

Leblhuber F
No affiliation info available
Reisecker F
No affiliation info available
Mayr WR
No affiliation info available
Deisenhammer E
No affiliation info available

MeSH

Charcot-Marie-Tooth DiseaseDiseases in TwinsDuffy Blood-Group SystemElectromyographyEvoked Potentials, VisualHereditary Sensory and Autonomic NeuropathiesHumansMaleMedian NerveMotor NeuronsMuscular AtrophyNeural ConductionOptic NervePedigreeReaction Time

Pub Type(s)

English Abstract
Journal Article

Language

ger

PubMed ID

3462518

Citation

Leblhuber, F, et al. "[Heterogeneity of Neural Muscular Atrophies]." Der Nervenarzt, vol. 57, no. 7, 1986, pp. 419-21.
Leblhuber F, Reisecker F, Mayr WR, et al. [Heterogeneity of neural muscular atrophies]. Nervenarzt. 1986;57(7):419-21.
Leblhuber, F., Reisecker, F., Mayr, W. R., & Deisenhammer, E. (1986). [Heterogeneity of neural muscular atrophies]. Der Nervenarzt, 57(7), 419-21.
Leblhuber F, et al. [Heterogeneity of Neural Muscular Atrophies]. Nervenarzt. 1986;57(7):419-21. PubMed PMID: 3462518.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - [Heterogeneity of neural muscular atrophies]. AU - Leblhuber,F, AU - Reisecker,F, AU - Mayr,W R, AU - Deisenhammer,E, PY - 1986/7/1/pubmed PY - 1986/7/1/medline PY - 1986/7/1/entrez SP - 419 EP - 21 JF - Der Nervenarzt JO - Nervenarzt VL - 57 IS - 7 N2 - Classification of the hereditary motor and sensory neuropathies is discussed and findings reported in the recent literature are compared to our own findings in a kinship with autosomal dominant CMT. Previous studies in CMT-families with comparable slow nerve conduction velocities had shown positive linkage of this hereditary neuropathy to the Duffy blood group locus; however, blood group typing in the recently studied kinship excluded close linkage, which may indicate the existence of another sub-group in this entity. Testing of visually evoked potentials in this kindred demonstrated significant differences in P 100 latencies of the families of twin brothers. This intrafamilial difference may also be an expression of heterogeneity. SN - 0028-2804 UR - https://www.unboundmedicine.com/medline/citation/3462518/[Heterogeneity_of_neural_muscular_atrophies]_ L2 - https://medlineplus.gov/charcotmarietoothdisease.html DB - PRIME DP - Unbound Medicine ER -