Meksyk - ludzie z zespołem Pradera-Williego - Sipa USA
EN_01282487_0067
*** World Rights ***
Jose Angel Mendieta (C), a six-year-old Mexican boy, attends an ophthalmology consultation with his mother (L) at the Federico Gomez Children's Hospital in Mexico City, Mexico on March 15, 2017. Jose Angel weighs 47 kilos (103.5 pounds) and stands 119 centimeters (3 feet 11 inches). He was diagnosed with Prader-Willi syndrome at age four, a process that took over two years. He lives with his mother. Prader-Willi Syndrome (PWS) is a rare genetic disorder caused by an abnormality in chromosome 15. In?newborns?symptoms include?weak muscle tone (hypotonia), poor appetite and slow development. In childhood the person experiences a sensation of constant hunger no matter how much he/she eats which often leads to?obesity?and?Type 2 diabetes. There may also be mild to moderate?intellectual impairment?and behavioral problems. Physical characteristics include a narrow forehead, small hands and feet, short in stature, and light skin color. Prader-Willi syndrome has no known cure. However, with early diagnosis and treatment such as growth hormone therapy, the condition may improve. Strict food supervision is typically required. PWS?affects an estimated 1 in 10,000 to 30,000 people worldwide. (Photo by Benedicte Desrus/Sipa USA)
2017-03-15
Benedicte Desrus/Sipa USA/East News
Sipa USA
Benedicte Desrus
sipausa_21272400
1,06MB
21cm x 14cm przy 300dpi
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