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Hereditary spastic paraplegia: from gene to clinic
IJCN-Iranian Journal of Child Neurology. 2010; 3 (4): 7-16
em Inglês | IMEMR | ID: emr-125342
ABSTRACT
Hereditary Spastic Paraplegia [HSP] is a degenerative disease of genetic origin affecting the corticospinal tracts in the spinal cord. There are three forms of inheritance Autosomal dominant HSP, Autosomal receive HSP and X-linked HSP. This disease is characterized by progressive spasticity of leg muscles with varying degrees of stiffness and weakness of other muscle groups. In this review, we will discuss the latest findings on the pathophysiology of axonal degeneration and all the responsible genetic defects in HSP
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Índice: IMEMR (Mediterrâneo Oriental) Assunto principal: Paraplegia Espástica Hereditária / Prevalência Tipo de estudo: Estudo de prevalência Limite: Humanos Idioma: Inglês Revista: Iran. J. Child Neurol. Ano de publicação: 2010

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Índice: IMEMR (Mediterrâneo Oriental) Assunto principal: Paraplegia Espástica Hereditária / Prevalência Tipo de estudo: Estudo de prevalência Limite: Humanos Idioma: Inglês Revista: Iran. J. Child Neurol. Ano de publicação: 2010