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Familial spastic paraplegia.
Article in English | IMSEAR | ID: sea-39341
ABSTRACT
Familial spastic paraplegia (FSP) was recorded in three families. The pattern of familial transmission and the onset in the second and third decade of life strongly suggested autosomal dominant inheritance. FSP in this series showed the consistent, classical, clinical features with some inconstant findings (nystagmus, dysarthria, posterior column involvement). Baclofen for the treatment of spasticity is beneficial in this condition and genetic counselling should be considered.
Subject(s)
Full text: Available Index: IMSEAR (South-East Asia) Main subject: Pedigree / Female / Humans / Male / Hereditary Sensory and Motor Neuropathy / Spastic Paraplegia, Hereditary / Adult / Middle Aged Language: English Year: 1989 Type: Article

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Full text: Available Index: IMSEAR (South-East Asia) Main subject: Pedigree / Female / Humans / Male / Hereditary Sensory and Motor Neuropathy / Spastic Paraplegia, Hereditary / Adult / Middle Aged Language: English Year: 1989 Type: Article