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Neurol India ; 2006 Sep; 54(3): 293-5
Artigo em Inglês | IMSEAR | ID: sea-120544

RESUMO

Severe childhood autosomal recessive muscular dystrophy (SCARMD) is characterized by a severe Duchene muscular dystrophy like phenotype. Most such cases represent alpha or gamma sarcoglycanopathies. Mental subnormality is very uncommon and other central nervous system deficits have not been documented in patients with SCARMD. We report a brother and sister with the SCARMD phenotype, who additionally had static mental subnormality and choreiform movements. Work-up for sarcolgycan genes, dystrophin gene and known causes of mental retardation and chorea was normal.


Assuntos
Criança , Coreia/etiologia , Saúde da Família , Feminino , Humanos , Masculino , Glicoproteínas de Membrana , Transtornos Mentais/etiologia , Distrofias Musculares/complicações , Sarcoglicanas
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