Dystrophia Myotonia Associated with Hemi-Analgesia
نویسندگان
چکیده
منابع مشابه
Dystrophia Myotonica Associated with Familial Paget’s Disease with Sarcomata
The skull in dystrophia myotonica-In a previous study of dystrophia myotonica Caughey and Brown (1950) suggested that the endocrine lesion was primarily a failure of the androgenic function of the adrenals and the gonads. In the same paper the authors reported the radiographic abnormalities in the skull in some patients with dystrophia myotonica. In subsequent papers Caughey (l952a and 1952b) r...
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The disorder of skeletal muscle known as myotonia has repeatedly attracted the interest of clinical neurophysiologists. The condition is characterized by a prolonged contraction ofmuscle fibres following voluntary exertion; alternatively it may be induced by direct or indirect electrical stimulation of muscle or by mechanical percussion of the muscle belly. The condition may be an accompanying ...
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Myotonia congenita (MC) is a skeletal muscle channelopathy characterized by inability of the muscle to relax following voluntary contraction. Worldwide population prevalence in humans is 1:100,000. Studies in mice, dogs, humans and goats confirmed myotonia associated with functional defects in chloride channels and mutations in a skeletal muscle chloride channel (CLCN1). CLCN1 encodes for the m...
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Objective and Importance: Developmental venous anomalies (DVAs) are common congenital anomalies of intracranial venous drainage. In general, it is felt that DVAs replace the normal venous drainage system and, unless associated with another lesion such as a cavernous malformation, should not produce symptoms. The present case raises important questions regarding the potential for DVAs to become ...
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ژورنال
عنوان ژورنال: Proceedings of the Royal Society of Medicine
سال: 1935
ISSN: 0035-9157
DOI: 10.1177/003591573502800522