hereditary spastic paraplegia sentence in Hindi
Sentences
Mobile
- 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.
- Recessively-inherited mutations in " NTE " that substantially reduce its catalytic activity cause a rare form of hereditary spastic paraplegia ( SPG39 ), in which distal parts of long spinal axons degenerate leading to limb weakness and paralysis.
- A mutation in this gene has been reported to be associated with Hereditary spastic paraplegia, however the Pathogenicity of the mutation, which may simply represent a Polymorphism ( biology ), is unclear . [ provided by RefSeq, Mar 2010 ].
- Diseases that can cause foot drop include direct hit to posterolateral neck of fibula, stroke, amyotrophic lateral sclerosis ( ALS or Lou Gehrig's Disease ), muscular dystrophy, Charcot Marie Tooth disease, multiple sclerosis, cerebral palsy, hereditary spastic paraplegia, Guillain Barr?syndrome and Friedreich's ataxia.
- These situations include those who have suffered meningitis, a congenital ( birth-originating ) brain infection, congenital hydrocephalus unrelated to the person's premature birth, a person who has suffered head trauma, or a person with some sort of familial disease ( e . g ., those with hereditary spastic paraplegia are said to not be SDR candidates ).
hereditary spastic paraplegia sentences in Hindi. What are the example sentences for hereditary spastic paraplegia? hereditary spastic paraplegia English meaning, translation, pronunciation, synonyms and example sentences are provided by Hindlish.com.