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Duchenneova svalová dystrofia
Č. záznamu d020388 Dátum 06.06.2025 Typ M - MESH Tematický termín Duchenneova svalová dystrofia Iný termín Angličtina (Pseudonym) Becker Muscular Dystrophy
Angličtina (Pseudonym) Duchenne Muscular Dystrophy
Angličtina (Pseudonym) Muscular Dystrophy, Becker
Angličtina (Pseudonym) Muscular Dystrophy, Pseudohypertrophic
Slovenčina (Pseudonym) Beckerova svalová dystrofia
Slovenčina (Pseudonym) dystrofia svalová pseudohypertrofická
Slovenčina (Pseudonym) Duchenneova pseudohypertrofická svalová dystrofia
Slovenčina (Pseudonym) Duchennova svalová dystrofia
Pozri tiež (Novšie záhlavie) dystrofín
(Skutočné meno) dystrofín
MDT C05.651.534.500.300C10.668.491.175.500.300C16.320.322.562C16.320.577.300 Poznámka 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) 
predmetové heslo
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