نتایج جستجو برای: congenital myasthenic syndrome
تعداد نتایج: 719275 فیلتر نتایج به سال:
It has been increasingly apparent in recent years that in addition to cases which fall into recognizable categories of muscle disease, a number of less common disorders occur from time to time which do not correspond to the accepted descriptions. Some of these appear to be metabolic in origin and can be elucidated, at least in part, by modern methods of investigation (McArdle, 1951) while other...
Fetal acetylcholine receptor inactivation syndrome is a rare condition occurring in newborns of myasthenic mothers, characterized by bulbar and facial weakness after recovery from the generalized muscle weakness. Antibodies against fetal subunit of acetylcholine receptor seem to have a pathogenetic role leading to long-lasting injury in vulnerable muscle groups. We report a girl, born to a myas...
The case of a 57-year-old woman with rheumatoid arthritis is presented to illustrate the rare occurrence of a myasthenic syndrome induced by D-penicillamine, which led to prolonged (5.25-h) postoperative apnoea necessitating artificial ventilation.
neuromuscular disorders encompass a broad spectrum of disorders from the anterior horn cell to the muscle tissue itself. the given condition can be either genetic or acquired. these group of disorders are diagnostically challenging as many of them also pose other systemic findings. one example would the commonly seen mental retardation in duchenne muscular dystrophy. from the practical point of...
Introduction True myasthenia gravis, as distinct from the myasthenic syndrome (Eaton-Lambert syndrome), has not been described in association with neoplastic disease other than malignant thymoma (Simpson, 1958). A case of ocular/bulbar myasthenia gravis occurring in a patient with breast carcinoma is described in which the temporal relationship between the disorders is such that the association...
P Richard, K Gaudon, F Andreux, E Yasaki, C Prioleau, S Bauché, A Barois, C Ioos, M Mayer, M C Routon, M Mokhtari, J P Leroy, E Fournier, B Hainque, J Koenig, M Fardeau, B Eymard, D Hantaï . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . ...
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