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Friends of Oliver: SoCal toddler with rare genetic disorder, DBA, inspires resiliency, research and hope

Parents of Oliver Nulsen, a toddler with Diamond-Blackfan anemia or DBA, are raising money for research in hopes of finding a breakthrough.

Despite help from Centre, patients with rare diseases, kin continue to suffer

Rare diseases are lifelong conditions. Approximately 95 per cent of them have no approved treatment. In cases where drugs are available, they are prohibitively exorbitant. Fakir, who earns less than Rs 10,000 per month, says his son's treatment costs Rs 30 lakh per annum.

Kids with Rare Genetic Disorders More Likely to Suffer Other Mental Health Problems

Challenging Life-saving Liver and Kidney Transplant Performed!

Challenging simultaneous liver and kidney transplant (that lasted 16 hours) bestows a 37-year-old woman (suffering from a rare genetic disorder) with a new lease of life.

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