leukodystrophy वाक्य
उदाहरण वाक्य
मोबाइल
- The MRI of patients with VWM shows a well defined leukodystrophy.
- He collaborated with the problems of people with leukodystrophy in Spain.
- An inherited genetic problem that exists in the breed is globoid cell leukodystrophy.
- Metachromatic leukodystrophy, like most enzyme deficiencies, has an autosomal recessive inheritance pattern.
- Brain MRI showed leukodystrophy with involvement of the cerebellar cortex and deep white matter.
- The degeneration of white matter can be seen in a MRI and used to diagnose leukodystrophy.
- Mutations in this gene have been associated with leukodystrophy dysmyelinating with spastic paraparesis with or without dystonia
- Three of the children had metachromatic leukodystrophy, which causes children to lose cognitive and motor skills.
- Mutations in this gene have been associated with Krabbe disease, also known as globoid cell leukodystrophy.
- In some patients, a progressive leukodystrophy has been observed that has a variable age of onset.
- Researchers in New York have successfully cured leukodystrophy in mice, using skin cells to repair damaged myelin sheaths.
- This then results in demyelination because of the buildup of sulfatide and is the main cause of Metachromatic Leukodystrophy.
- In addition, many research groups are studying the cellular processes of myelination, which may provide insights into leukodystrophy.
- Disorders involving dysfunctional COX assembly via gene mutations include Leigh syndrome, cardiomyopathy, leukodystrophy, anemia, and sensorineural deafness.
- Leukodystrophy is characterized by specific symptoms including decreased motor function, muscle rigidity, and eventually degeneration of sight and hearing.
- He has worked beneficially for years for homeless children or leukodystrophy problems so it has been awarded the 2011 ELA Prize.
- For more on this story, metachromatic leukodystrophy and related links, go to http : / / www . ajc . com
- The girls, healthy until two years ago, have been rendered helpless by a rare and fatal genetic disease called metachromatic leukodystrophy.
- Jim Frank, who lives nearby, brought his 11-year-old grandson, Louden, in a wheelchair with leukodystrophy.
- In humans, Cockayne syndrome ( CS ) is a rare autosomal recessive leukodystrophy ( associated with the degradation of white matter ).
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