Distrofia muscular de Becker: relato de caso e revisão de literatura

Authors

  • Maria Bernadete Renoldi Oliveira Gavi Universidade Federal do Espírito Santo - UFES
  • Manoel Neves Pimentel Universidade Federal do Espírito Santo - UFES
  • Marcelo Nogueira Silva Universidade Federal do Espírito Santo - UFES
  • Eliete Rabbi Bortolini Universidade Federal do Espírito Santo - UFES
  • Alípio Cesar Nascimento Universidade Federal do Espírito Santo - UFES

DOI:

https://doi.org/10.11606/issn.2317-0190.v3i3a102031

Keywords:

Becker Muscular Dystrophy, Myopathies, Physiotherapy

Abstract

Muscular Dystrophies are uncommon diseases and unknown by some physicians. We present a patient with the diagnosis of Becker Muscular Dystrophy in advanced stage with conspicuous physical findings, compatible family and pas t hi story and characteristic muscular biopsy. Although the DNA analysis didn't show deletions in the implied gene, the diagnosis was c1inically confirmed. We related some differential diagnosis and discussed the therapeutic aspects. These diseases must be considered in all patients with muscular weakness, specially children, regarding the need of a precocious physiatric and genetic counseling.

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References

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Published

1996-12-17

Issue

Section

Review Article

How to Cite

1.
Gavi MBRO, Pimentel MN, Silva MN, Bortolini ER, Nascimento AC. Distrofia muscular de Becker: relato de caso e revisão de literatura. Acta Fisiátr. [Internet]. 1996 Dec. 17 [cited 2024 May 29];3(3):18-23. Available from: https://revistas.usp.br/actafisiatrica/article/view/102031