Një rast i dhimbshëm/Motër e vëlla të prekur nga sëmundja që shkakton plakje të parakohshme
Dy fëmijë në Ranchi të Indisë, vëlla e motër, janë prekur nga “Cutis Laxa”, një sëmundje e rrallë degjenerative që shkakton plakjen. Djali është 18 muajsh, kurse e motra 7 vjeç vuajnë edhe nga Progria që shoqërohet edhe me dhimbje. Rasti, përveçse i dhimbshëm, ka krijuar habi, pasi as prindërit, as e motra e madhe të dy fëmijëve, nuk kanë asnjë problem.
Watch this heartbreaking video about two children with a rare aging disease in IndiaTwo Indian children with Cutis Laxa, a rare degenerative disease, which causes them to appear prematurely aged, were taken by their parents for medical testing in Sadar hospital, in Ranchi on Saturday.The 18 month-old boy and his seven-year-old sister suffer from the rare condition as well as a form of Progeria for which no cure exists. The pair suffers from pain in their joints, swollen faces, and wrinkled skin.Progeria is a disorder that causes children to age rapidly starting from age two, most of those afflicted die from heart problems in early adolescence. Neither the children's parents nor the pair's 13-year-old sister suffer from the condition, leaving doctors puzzled as to the origins of the disease.
Posted by Press TV on Saturday, February 6, 2016
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