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・ Central District (Bahmai County)
・ Central District (Bajestan County)
・ Central District (Bakharz County)
・ Central District (Bam County)
・ Central District (Bampur County)
・ Central District (Bandar Abbas County)
・ Central District (Bandar Lengeh County)
・ Central consonant
・ Central Contra Costa Sanitary District
・ Central Control Commission
・ Central Control Commission of the Communist Party of the Soviet Union
・ Central Cooperative Bank
・ Central Coordination Group for Hong Kong and Macau Affairs
・ Central cord syndrome
・ Central Core
Central core disease
・ Central core disease of muscle
・ Central Core Historic District
・ Central Corridor
・ Central Corridor (Union Pacific Railroad)
・ Central Corridor Coordinating Committee
・ Central Corridor Rail Line
・ Central Cotton Research Institute
・ Central council
・ Central Council for Education and Training in Social Work
・ Central Council of Afghan Trade Unions
・ Central Council of Ex-Muslims
・ Central Council of German Sinti and Roma
・ Central Council of Homoeopathy
・ Central Council of Homoeopathy Act, 1973


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Central core disease : ウィキペディア英語版
Central core disease

Central core disease (CCD), also known as central core myopathy, is an autosomal dominant congenital myopathy (inborn muscle disorder). It was first described by Shy and Magee in 1956. It is characterized by the appearance of the myofibril under the microscope.
==Signs and symptoms==
The symptoms of CCD are variable, but usually involve hypotonia (decreased muscle tone) at birth, mild delay in child development (highly variable between cases), weakness of the facial muscles, and skeletal malformations such as scoliosis and hip dislocation.〔
Symptoms may be present at birth or may appear at any stage of life. There appears to be a growing number of people who do not become symptomatic until adulthood to middle age. While generally not progressive, again there appears to be a growing number of people who do experience a slow clinically significant progression of symptomatology. These cases may hypothetically be due to the large number of gene mutations of ryanodine receptor malfunction, and with continued research may in fact be found to be clinical variants.

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