CASE SERIES OF FAMILIAL (HEREDITARY) SPASTIC PARAPLEGIA

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YAZDAN PANAH P.

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

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Journal: Journal of Mazandaran University of Medical Sciences Year:2007 | Volume:17 | Issue:58 Page(s): 129-133

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Information Journal Paper

Title

CASE SERIES OF FAMILIAL (HEREDITARY) SPASTIC PARAPLEGIA

Author(s)

YAZDAN PANAH P. | Issue Writer Certificate

Keywords

SPASTICITYQ3

PARAPLEGIAQ3

MOTOR NEURON DISEASEQ3

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.

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APA: Copy

YAZDAN PANAH, P.. (2007). CASE SERIES OF FAMILIAL (HEREDITARY) SPASTIC PARAPLEGIA. JOURNAL OF MAZANDARAN UNIVERSITY OF MEDICAL SCIENCES, 17(58), 129-133. SID. https://sid.ir/paper/45108/en

Vancouver: Copy

YAZDAN PANAH P.. CASE SERIES OF FAMILIAL (HEREDITARY) SPASTIC PARAPLEGIA. JOURNAL OF MAZANDARAN UNIVERSITY OF MEDICAL SCIENCES[Internet]. 2007;17(58):129-133. Available from: https://sid.ir/paper/45108/en

IEEE: Copy

P. YAZDAN PANAH, “CASE SERIES OF FAMILIAL (HEREDITARY) SPASTIC PARAPLEGIA,” JOURNAL OF MAZANDARAN UNIVERSITY OF MEDICAL SCIENCES, vol. 17, no. 58, pp. 129–133, 2007, [Online]. Available: https://sid.ir/paper/45108/en

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