Posts Tagged ‘rare genetic condition’

At VIVA! we’ve been busily researching Progeria, also known as the Hutchinson-Gilford Progeria Syndrome, and assisting our GLOBALHealthPR partners in a worldwide search for children diagnosed with the condition. Progeria is a rare and fatal genetic condition that causes rapid ageing in young children. Progeria symptoms include growth failure, loss of body fat and hair,…