[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.
MeSH
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 -