| • आनुवंशिक संस्तंभी अधरांगघात | |
| hereditary: आनुवंशिक प्रतिभा | |
| spastic: संस्तंभता से | |
| spastic paraplegia: संस्तंभी | |
| paraplegia: अधरांगघात | |
hereditary spastic paraplegia मीनिंग इन हिंदी
hereditary spastic paraplegia उदाहरण वाक्य
उदाहरण वाक्य
अधिक: आगे- The paraplegin gene is responsible for an autosomal recessive form of hereditary spastic paraplegia.
- This is the case in Friedreich's ataxia, hereditary spastic paraplegia, and Wilson's disease.
- Additionally the loss of its production appears to be one cause of the human neurological disease, Hereditary spastic paraplegia.
- Together with French physician Maurice Lorrain, the eponymous Str�mpell Lorrain disease is named, which is an hereditary spastic paraplegia.
- This gene is a candidate gene for other hereditary spastic paraplegias or neurodegenerative disorders as well as spastic ataxia-neuropathy syndrome.
- Hereditary spastic paraplegias ( HSPs ) are a group of inherited neurological disorders which are characterized by progressive spasticity and weakness of the lower extremities.
- Mutations in the " ATL1 " gene are also a common cause of early-onset hereditary spastic paraplegia ( HSP ) in humans.
- Hereditary spastic paraplegia was first described in 1883 by Adolph Str�mpell, a German neurologist, and was later described more extensively in 1888 by Maurice Lorrain, a French physician.
- A second homozygous enzyme-disabling mutation has been identified in CYP2U1, c . 1A > C / p . Met1 ?, that is associated with < 1 % of hereditary spastic paraplegia sufferers.
- A mutation ( c . 947A > T ) in CYP2U1 has been associated in a very small number of patients with Hereditary spastic paraplegia in that it segregates with the disease at the homozygous state in two afflicted families.
