First Black Child with Aging Disease 12-year-old Ontlametse Phalatse, a South African is the first black child to be diagnosed with the aging disease progeria, a rare and fatal genetic condition that rushes up her aging process. According to some news, in spite of some of the girls in her school aren't kind to her, Ontlametse Phalatse says she doesn't mind, instead the child with the big personality and bright smile calls herself "the first lady" and lives in a dream world about a future that may never come. As for Ontlametse's mother named Bellon Phalatse, her baby was born looking normal but she realized early on that something was wrong. The baby suffered constant rashes and by the time she was 3 months old, Phalatse thought she had a skin disease. Before Ontlametse's first birthday, her mother added: "Her hair was falling, her nails weren't normal, the skin problems, we were going up and down to the doctors." As the child aged prematurely, her father abandoned the family when Ontlametse was 3 years old. Interestingly, in a two-year campaign to identify children with this kind of disease, the Progeria Research Foundation announced the number of children diagnosed around the world has risen up to 48 percent, from 54 to 80, on five continents. The foundation said more than two South Africans have been diagnosed and that two including Phalatse remain alive.
Ontlametse Phalatse is the only known black female born with the extremely rare premature aging disease