Topic: Types of Paraplegia
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Answers to Common Questions
What type of disibility is paraplegia?
Paraplegia is caused by trauma or disease of the spinal cord below the cervical portion of the spinal cord. Read More »
Source: http://wiki.answers.com/Q/What_type_of_disibility_is_paraplegia
What is spastic paraplegia type 11?
Spastic paraplegia type 11 is part of a group of genetic disorders known as hereditary spastic paraplegias. These disorders are characterized by progressive muscle stiffness (spasticity) and the development of paralysis of the lower limbs (... Read More »
Source: http://ghr.nlm.nih.gov/condition/spastic-paraplegia-type-11
What is spastic paraplegia type 3A?
Spastic paraplegia type 3A is part of a group of genetic disorders known as hereditary spastic paraplegias. These disorders are characterized by progressive muscle stiffness (spasticity) and the development of paralysis of the lower limbs (... Read More »
Source: http://ghr.nlm.nih.gov/condition=spastic-paraplegia-type-3a
More Common Questions
Answers to Other Common Questions
Spastic paraplegia type 4 is part of a group of genetic disorders known as hereditary spastic paraplegias. These disorders are characterized by progressive muscle stiffness (spasticity) and the development of paralysis of the lower limbs (p...
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Source: http://ghr.nlm.nih.gov/condition=spastic-paraplegia-type-4
Spastic paraplegia type 2 is part of a group of genetic disorders known as hereditary spastic paraplegias. These disorders are characterized by progressive muscle stiffness (spasticity) and the development of paralysis of the lower limbs (p...
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Source: http://ghr.nlm.nih.gov/condition=spastic-paraplegia-type-2
Symptoms of spastic paraplegia type 3A commonly appear before the age of 10. The specific incidence of this disorder is unknown.
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Source: http://ghr.nlm.nih.gov/condition/spastic-paraplegia-type-3a
Mutations in the ATL1 gene cause spastic paraplegia type 3A. The ATL1 gene provides instructions for producing a protein called atlastin-1. Atlastin-1 is found throughout the body, particularly in the brain. In cells, this protein is found ...
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Source: http://ghr.nlm.nih.gov/condition/spastic-paraplegia-type-3a
Mutations in the PLP1 gene cause spastic paraplegia 2. The PLP1 gene provides instructions for producing proteolipid protein 1 and a modified version (isoform) of proteolipid protein 1, called DM20. Proteolipid protein 1 and DM20 are primar...
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Source: http://ghr.nlm.nih.gov/condition=spastic-paraplegia-type-2
The prevalence of all hereditary spastic paraplegias combined is estimated to be 2 to 6 in 100,000 people worldwide. Spastic paraplegia type 2 likely accounts for only a small percentage of all spastic paraplegia cases.
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Source: http://ghr.nlm.nih.gov/condition=spastic-paraplegia-type-2
The prevalence of spastic paraplegia type 4 is estimated to be 2 to 6 in 100,000 people worldwide.
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Source: http://ghr.nlm.nih.gov/condition=spastic-paraplegia-type-4