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Phenotypic and immunohistochemical characterization of sarcoglycanopathies
(Faculdade de Medicina / USP, 2011)
INTRODUCTION: Limb-girdle muscular dystrophy presents with heterogeneous clinical and molecular features. The primary characteristic of this disorder is proximal muscular weakness with variable age of onset, speed of ...
Distrofia muscular congênita estudo clinico de 17 pacientes
(Academia Brasileira de Neurologia - ABNEURO, 1991-09-01)
We concur with the idea that congenital muscular dystrophy (CMD) is a distinct clinical entity, and report 17 patients (2 negroes and 15 whites; 12M and 5 F; median age 6 years, range 1 to 24 years) with genetic, clinical, ...