Congenital anomalies associated with arthrogry- posis multiple congenita. Características gerais dos pacientes com artrogripose múltipla congênita. Items 51 – 88 of 88 Resumo: Objetivo: A Artrogripose múltipla congênita é uma síndrome neuromuscular relativamente rara, com prevalência de Items 51 – 88 of 88 Aplasia cutis congenita (ACC) is a skin condition of rare Resumo: Objetivo: A Artrogripose múltipla congênita é uma síndrome.
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In addition, it is based on Medline and on the review of the most recent numbers of Neuromuscular Disorders, the official journal of the World Muscle Society.
Summary of the findings: Nowadays many new diagnostic methods, including techniques of fetal diagnosis, and a more objective genotype-phenotype correlation as well as classification are available.
Amiotrofia espinal infantil AEI.
artrogripoe Atualmente, conhecem-se pelo menos quatro genes implicados 2q22, nebulina; 1q22, alfa-tropomiosina; 9p13, beta-tropomiosina; 1q42, alfa-actina. Muscle disorders in childhood. Talbot K, Davies KE. J Neurol Sci ; Spinal muscular atrophy – clinical and genetic correlations. Identification and characterization of a spinal muscular atrophy-determining gene.
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Arthrogryposis – Wikipedia
Molecular genetics of hereditary neuropathies. Childhood chronic inflammatory demyelinating polyneuropathy: Quinidine sulfate therapy for the slow-channel congenital myasthenic syndrome.
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Carlos Gomes, cj. How to cite this article.