Spinal and bulbar muscular atrophy with pseudomyotonia phenomena: a clinical case report

Spinal and bulbar muscular atrophy with pseudomyotonia phenomena: a clinical case report

A clinical description of a 28-year-old man with spinal and bulbar muscular atrophy diagnosed on the basis of the CAG-trinucleotide expansion in the gene coding androgen receptor is presented. He exhibited skeletal muscles and tongue fasciculations, gynecomastia, increased serum testosterone and cre...

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Bibliographic Details
Main Authors: S. S. Nikitin, V. N. Grigoryeva, K. A. Mashkovich, O. L. Mironovich, N. V. Ryadninskaya, A. V. Polyakov
Format: Article
Language:Russian
Published: ABV-press 2020-01-01
Series:Nervno-Myšečnye Bolezni
Subjects:
spinal and bulbar muscle atrophy
spinal and bulbar muscular atrophy
kennedy’s disease
motor neuron disease
myotonia
myopathy
multiple system involvement
Online Access:https://nmb.abvpress.ru/jour/article/view/353

Internet

https://nmb.abvpress.ru/jour/article/view/353

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