telangiectasia वाक्य
उदाहरण वाक्य
मोबाइल
- The gene is called ATM ( for ataxia telangiectasia mutated ).
- The natural history of macular telangiectasia suggests a slowly progressive disorder.
- The late appearance of telangiectasia may be a barrier to the diagnosis.
- A major research interest has been the disease, hereditary hemorrhagic telangiectasia.
- :Another condition which might fit the description is telangiectasia aka spider veins.
- Joey suffers from Ataxia-Telangiectasia, or AT, a rare genetic disorder.
- Telangiectasia is a component of the esophageal dysmotility, sclerodactyly, and telangiectasia ).
- Telangiectasia is a component of the esophageal dysmotility, sclerodactyly, and telangiectasia ).
- Reduced activity of this enzyme may also play a role in ataxia-telangiectasia.
- Another condition, the gene for which was discovered earlier this year, is ataxia telangiectasia.
- House wakes up and correctly diagnoses the patient with hereditary hemorrhagic telangiectasia, surprising the team.
- Conditions often treated include venous stasis ulcers, varicose veins and spider veins ( telangiectasia ).
- One of the hallmarks of ataxia telangiectasia is that cells of patients are extremely sensitive to radiation.
- It may also function in the suppression of radiosensitivity since it is associated with ataxia telangiectasia phenotype.
- Mutations in GDF2 have been identified in patients with a vascular disorder phenotypically overlapping with hereditary hemorrhagic telangiectasia.
- Mutations in this gene have been associated with recessive and dominant forms of hypotrichosis-lymphedema-telangiectasia.
- Some telangiectasia are due to developmental abnormalities that can closely mimic the behaviour of benign blanch when tested with diascopy.
- Sclerodactyly is a component of the esophageal dysmotility, "'sclerodactyly "', and telangiectasia .)
- OWR is a legitamite abbreviation for Osler-Weber-Rendu Syndrome which is also known as Hereditary hemorrhagic telangiectasia.
- Macular telangiectasia ( MacTel ) type 1 is a very rare disease, typically unilateral and usually affecting male patients.
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