Case series of Familial (Hereditary) Spastic Paraplegia

Yazdanpanah, P (2007) Case series of Familial (Hereditary) Spastic Paraplegia. Journal of Mazandaran University of Medical Sciences, 17 (58). pp. 129-133.

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Official URL: http://jmums.mazums.ac.ir/article-1-222-en.html

Abstract

The familial spastic paraplegia (FSP) is a heterogeneous group of motor neuron disorders characterized by slow progressive weakness and spasticity of lower limbs. The disorder can appear at any age, but it usually occurs in childhood or early adult life. The genetic pattern of this disease is mainly autosomal dominant trait, but occasionally as an autosomal recessive trait, and very rarely as an X-linked recessive disease. The prevalence of this disease ranges from 2.0 to 4.3 per 100000. In this study, there were 5 patients in a family and 3 in another family who had weakness and spasticity of lower limbs in the first decade of their life. In physical examination, there were normal sensation, ankles spasticity, extensor plantar reflexes, deep tendon reflexes 4.2, tip toe walking, contracture of knees and ankles. Genetic pattern of disease was these patients is autosomal dominant trait.

Item Type: Article
Uncontrolled Keywords: Spasticity, Paraplegia, Motor neuron disease
Depositing User: Unnamed user with email eprints@mazums.ac.ir
Date Deposited: 04 Jan 2018 17:52
Last Modified: 04 Jan 2018 17:52
URI: http://eprints.mazums.ac.ir/id/eprint/3190

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