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Created by: architected

Number of Blossarys: 27

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Leber's hereditary optic neuropathy is a genetic defect, which can lead to optic nerve damage or neuropathy, is called by roughly one in every 9,000 people. Around 50 per cent of men and 80 per cent of women with the disorder will suffer no loss of vision. The main symptom is the sudden loss of vision, which is caused by a death of cells in the optic nerve responsible for relaying visual information from the eyes to the brain. Once cells start dying, affected eyes will begin seeing colours that appear more washed out. Within a period of eight weeks, it can lead to near or total blindness.

Domain: Medical; Health care; Category: Medicine

Leber ir iedzimta optikas neiropātija ir ģenētisks defekts, kas var novest pie redzes nervu bojājumiem vai neiropātiju, sauc par aptuveni vienu reizi 9000 cilvēku. Aptuveni 50 procentiem vīriešu un 80 procenti sieviešu ar traucējumiem cieš bez redzes zudums. Galvenais simptoms ir Pēkšņs samaņas vīziju, kuru izraisa redzes nervu, kas atbild par izklāšanas vizuālo informāciju no acīm uz smadzeņu šūnas nāvi. Kad šūnas sāk mirt, skartā acis sāks redzēt krāsu, kas parādās vairāk izbalējušu. Astoņu nedēļu laikā, tā var novest pie gandrīz vai kopējo aklumu.

Domain: Medical; Health care; Category: Medicine

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