optic atrophy वाक्य
उदाहरण वाक्य
मोबाइल
- Progressive optic atrophy may result in decreased visual acuity or color vision.
- Visual examination shows optic atrophy and an increase in the blind spot.
- In some cases, Dominant optic atrophy may remain subclinical until early adulthood.
- Progression of dominant optic atrophy varies even within the same family.
- Other ocular defects including optic atrophy, microphthalmia, vitreitis, leukokoria and cataracts can also be seen.
- It consists of diabetes insipidus, diabetes mellitus, optic atrophy, and deafness, hence the acronym DIDMOAD.
- Nanri suffered a sudden onset of optic atrophy in 1953 and nearly lost his sight.
- Neurological symptoms of BVVL include optic atrophy, cerebellar ataxia, retinitis pigmentosa, epilepsy and autonomic dysfunction.
- This typically evolves to very severe optic atrophy and a permanent decrease of visual acuity.
- Optic atrophy occurs in the first year and the following symptoms show up before thirteen years.
- A nonsense mutation in the TMEM126A gene has been shown to be related to optic atrophy.
- Optic nerve involvement in Beh�et's disease is rare, typically presenting as progressive optic atrophy and visual loss.
- Manipulation of the optic atrophy 1 ( Opa1 ) gene had interesting effects on fusion between mitochondria.
- In the differential diagnosis, other macular dystrophies as well as the hereditary optic atrophies must be considered.
- When treated with vitamin, patients with Leber's disease may suffer serious optic atrophy, possibly leading to blindness.
- Other possible associations include corneal defects, congenital pulmonary stenosis, total anomalous pulmonary venous connection deafness and optic atrophy.
- Mutations in OPA1 also cause optic atrophy, which suggests a common role of mitochondrial fusion in neuronal dysfunction.
- Longstanding papilledema leads to optic atrophy, in which the disc looks pale and visual loss tends to be advanced.
- In the later onset form, patients typically have normal intellectual function, but present with spastic diplegia and optic atrophy.
- While the symptoms of CMT2A are variable they are characterized by a sometimes early onset, severe phenotype, and optic atrophy.
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