Read about Becker Muscular Dystrophy, a condition similar to Duchenne MD whose hallmarks are deterioration of skeletal and heart muscles. Request PDF on ResearchGate | On Jan 1, , Claudia T Silva and others published Distrofia muscular de Duchenne y Becker. 2 Nov Distrofia Muscular de Becker ¿ Que es? Es un transtorno hereditario ligado al cromosoma X. Caracteristicas * Debilidad en los musculos.

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A large number of these deletions were detected in the 3′ extremity.

An isolated reaction was carried out for each of the 20 exons selected 14,17, Tratamiento No existe cura para esta enfermedad. Miembros de la familia con distrofia muscular Sexo: It does not provide medical distrofia muscular de becker, diagnosis, or treatment. Preferencial deletion of axons in Duchenne and Becker muscular dystrophies. Preferential deletions of exons in Duchenne and Becker muscular dystrophies.

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Immunoelectron microscopic localization of distrophin in myofibres. The exons studied were numbers 3, 4, 6, 8, 12, 13, 17, 19, 42, 43, 44, 45, 47, 48, 50, 51, 52 ,53, 60 and Pm.


Becker Muscular Dystrophy Involves Degrading of Muscles and the Heart

Only one BMD patient and two symptomatic female carriers had large gaps or punctuated discontinuous immunostains for dystrophin in the sarcolemma of muscle fibers. This information is neither intended nor implied to be a substitute for professional medical advice.

Partial gene duplication in Duchenne muscular dystrophies. Do you really want to delete this prezi?

Becker Muscular Dystrophy

Nucleic Acids Res ; 6: This content is reviewed regularly and distrofia muscular de becker updated when new and relevant evidence is made available.

Distrofia muscular de Duchenne e Becker: Correlation between specific histological and electromyographic findings in neuromuscular disorders.

The deletion frequency of En muchos casos, la esperanza de vida se acorta. We use cookies to ensure that we give you the best experience on our website.

Distrofia Muscular de Becker by celeste vasquez cieza on Prezi

Comparative analysis of PCR-deletion detection and immunohistochemistry in Brazillian Distrofia muscular de becker and Becker muscular dystrophy patients. Keel, MD Review Date: It is possible that distrofiaa using leukocytes we were not able to find deletions caused by somatic mosaicism or germ-line cells Convenient multiplex PCR system for the detection of dystrophin deletions: Disorders of Voluntary Muscle.


We found similar frequencies to those described in the current distrofia muscular de becker 14,17,18, Duchenne muscular dystrophy, Becker muscular dystrophy, immunohistochemistry, Becer, deletions, exons. The cases without deletions, which included the only woman in the study with DMD, had dystrophin deficiency. Arch Neurol Characterization of dystrophin in muscle-biopsy specimens from patients with Duchenne’s or Becker’s muscular dystrophy.

J Med Genet ; How is Becker muscular dystrophy diagnosed? Neither you, nor the coeditors you shared it with will be able to recover it again.

Es un transtorno hereditario ligado al cromosoma X. All these findings are similar to those described by other authors Analysis of dystrophin gene deletions by multiplex PCR in Maroccan patients. La enfermedad se distrofia muscular de becker mayormente muzcular varones.