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DESCRIBEN EL TRATAMIENTO CON CORTICOIDES EN PACIENTES CON DISTROFIA MUSCULAR DE DUCHENNE (especial para SIIC © Derechos reservados) |
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Autor: David Feder Columnista Experto de SIIC Institución: Faculdade de Medicina do ABC Artículos publicados por David Feder |
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Coautores Panosso Macedo Luiza* Schewed Razaboni Renata** Wohlers Sabo Helena** Perez Sacardo Karina** Aluna do 3º ano do curso de medicina, Faculdade de Medicina do ABC, São Paulo, Brasil* |
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Recepción del artículo 14 de abril, 2009 |
Aprobación 27 de abril, 2009 |
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Primera edición 19 de octubre, 2009 |
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A distrofia muscular de Duchenne (DMD) é uma doença recessiva ligada ao cromossomo X (na região p21) que ocorre por uma mutação no gene responsável pela síntese da proteína distrofina que resulta em uma quantidade muito reduzida, nula ou em uma forma anormal dessa proteína. Até que a terapia molecular possa ser obtida somente os corticóides aumentaram temporariamente a função muscular. São utilizados os seguintes corticóides: prednisona e prednisolona (0.75 mg/kg) e deflazacort (0.9 mg/kg). Os corticóides aumentam massa muscular, retardam a velocidade de degeneração muscular, aumentam o tempo de deambulação e também a capacidade respiratória e cardíaca. No entanto, esteróides possuem diversos efeitos colaterais. O deflazacort causa menos efeitos colaterais, exceto a catarata. Os efeitos benéficos e colaterais dos corticóides precisam ser monitorizados de perto. distrofia muscular de Duchenne, cromossomo X, corticostróides, distrofia muscular de Duchenne, corticosteroides, prednisona, deflazacort Clasificación en siicsalud Artículos originales > Expertos de Iberoamérica > página www.siicsalud.com/des/expertocompleto.php/103722 Especialidades David Feder, Faculdade de Medicina do ABC, São Paulo, Brasil, E-mail: david-feder@uol.com.br
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