arch9
EN_01094675_0418
In this picture taken 25 January 2005, The hands of Indian Progeria affected child Ekramul Khan are held by his father as they pose outside a clinic in Calcutta. Only 48 cases of what is formally known as Hutchinson-Gilford progeria syndrome exist in the world, an extremely rare condition causing the body to fast-forward through the ageing process. This family's case unique is it is the only known example where more than one family member suffers from the disease. A team led by paediatrician Dr Chandan Chattopadhyay studied the family for two years and concluded progeria was an inherited and recessive condition. AFP PHOTO/ Deshakalyan CHOWDHURY
Minimum price 50PLN
2005-01-25
AFP/EAST NEWS
AFP
DESHAKALYAN CHOWDHURY
000_HKG2005051575611
0,71MB
17cm x 11cm przy 300dpi
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