Neuropathy sensory spastic paraplegia

Common Name(s)

Neuropathy sensory spastic paraplegia

Description for this condition is not yet available.
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Neuropathy sensory spastic paraplegia" for support, advocacy or research.

There are currently no organizations listed in Disease InfoSearch that support this condition. Create a listing.

 

 

General Support Organizations

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Neuropathy sensory spastic paraplegia" returned 3 free, full-text research articles on human participants. First 3 results:

Mutation in the epsilon subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct5) gene causes autosomal recessive mutilating sensory neuropathy with spastic paraplegia.
 

Author(s): A Bouhouche, A Benomar, N Bouslam, T Chkili, M Yahyaoui

Journal: J. Med. Genet.. 2006 May;43(5):441-3.

 

Mutilating sensory neuropathy with spastic paraplegia is a very rare disease with both autosomal dominant and recessive modes of inheritance. We previously mapped the locus of the autosomal recessive form to a 25 cM interval between markers D5S2048 and D5S648 on chromosome 5p. In ...

Last Updated: 1 May 2006

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Autosomal recessive mutilating sensory neuropathy with spastic paraplegia maps to chromosome 5p15.31-14.1.
 

Author(s): Ahmed Bouhouche, Ali Benomar, Naima Bouslam, Reda Ouazzani, Taïeb Chkili, Mohamed Yahyaoui

Journal: Eur. J. Hum. Genet.. 2006 Feb;14(2):249-52.

 

Autosomal recessive ulcero-mutilating neuropathy with spastic paraplegia is a very rare disease since only few cases were described up to date. We report in this study a consanguineous Moroccan family with four affected males with this syndrome. The disease onset was in early infancy, ...

Last Updated: 19 Jan 2006

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Spastic paraplegia with amyotrophy of the legs: a rare case of motor and sensory neuropathy.
 

Author(s): Y Izumi, Y Fukuuchi, A Koto, N Ishihara, H Tachibana

Journal: Keio J Med. 1994 Dec;43(4):206-10.

 

A 36-year-old man who suffers from gait disturbance is reported. He noticed deformity of his feet at the age of 15. When he was 32 years old, he complained of heaviness in his lower extremities. Since then his legs have been always stiff. He had no previous illness or familial neuromuscular ...

Last Updated: 23 Mar 1995

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Reviews from the PubMed Database

Review articles summarize what is currently known about a disease. They discuss research previously published by others.
The terms "Neuropathy sensory spastic paraplegia" returned 1 free, full-text review articles on human participants. First 3 results:

Sensory neuropathy in hereditary spastic paraplegia.
 

Author(s): W Schady, C M Smith

Journal: J. Neurol. Neurosurg. Psychiatr.. 1994 Jun;57(6):693-8.

 

A large kinship is reported with dominantly inherited spastic paraplegia starting in the first decade of life; its clinical evolution was indistinguishable from that of "pure" hereditary spastic paraplegia (HSP). However, all patients studied had electrophysiological evidence of a ...

Last Updated: 15 Jul 1994

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Clinical Trial Information This information is provided by ClinicalTrials.gov

Genetic and Physical Study of Childhood Nerve and Muscle Disorders
 

Status: Recruiting

Condition Summary: Muscular Dystrophies; Muscle Myopathies; Hereditary Spastic Paraplegias; Inherited Neuropathies; Inherited Neuromuscular Conditions

 

Last Updated: 30 Jun 2017

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Disease Natural History and Biomarkers of SPG3A, SPG4A, and SPG31
 

Status: Recruiting

Condition Summary: Hereditary Spastic Paraplegia

 

Last Updated: 30 Jun 2017

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The Pre-SPG4 Study
 

Status: Recruiting

Condition Summary: Hereditary Spastic Paraplegia; Hereditary, Spastic Paraplegia, Autosomal Dominant

 

Last Updated: 2 Jul 2017

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