Open AccessDifferential diagnosis of hypokinetic disorders in hereditary neuromuscular diseases
Author(s) -
Л А Сайкова,
В Д Косачев,
В. Г. Пустозеров,
Т. М. Алексеева,
Т. N. Vasilyeva,
I. G. Zavolokov
Publication year - 1997
Publication title -
nevrologičeskij vestnik
Language(s) - English
Resource type - Journals
eISSN - 2304-3067
pISSN - 1027-4898
DOI - 10.17816/nb79927
Subject(s) - polymyositis , differential diagnosis , medicine , amyotrophy , physical medicine and rehabilitation , pathology , atrophy
For determination criteria of differential diagnosis analysis of clinical manifestations and indices of additional research methods (EMG, ENMY, biochemical, histomorphological) of paroxysmal hypokinetic conditions in myoplegia, myopathic syndromes, glycogenosis and Mc Ardl syndrome in polymyositis, Eulenburg-Lewandowsky paramyotoxia, remittent form of neural amyotrophy, some forms of congenital myopathies was carried out.