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Duchenneova svalová dystrofia
Record number d020388 Date 06.06.2025 Type M - MESH Topical term Duchenneova svalová dystrofia Other term English (Pseudonym) Becker Muscular Dystrophy
English (Pseudonym) Duchenne Muscular Dystrophy
English (Pseudonym) Muscular Dystrophy, Becker
English (Pseudonym) Muscular Dystrophy, Pseudohypertrophic
Slovak (Pseudonym) Beckerova svalová dystrofia
Slovak (Pseudonym) dystrofia svalová pseudohypertrofická
Slovak (Pseudonym) Duchenneova pseudohypertrofická svalová dystrofia
Slovak (Pseudonym) Duchennova svalová dystrofia
See also (Later heading) dystrofín
(Skutočné meno) dystrofín
UDC C05.651.534.500.300C10.668.491.175.500.300C16.320.322.562C16.320.577.300 Note An X-linked recessive muscle disease caused by an inability to synthesize DYSTROPHIN, which is involved with maintaining the integrity of the sarcolemma. Muscle fibers undergo a process that features degeneration and regeneration. Clinical manifestations include proximal weakness in the first few years of life, pseudohypertrophy, cardiomyopathy (see MYOCARDIAL DISEASES), and an increased incidence of impaired mentation. Becker muscular dystrophy is a closely related condition featuring a later onset of disease (usually adolescence) and a slowly progressive course. (Adams et al., Principles of Neurology, 6th ed, p1415) 
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