Every rare disease tells a story. Understanding how one unfolds — how it develops and evolves — is often the first step toward treating it. A small genetic error, a malfunctioning cell or a breakdown in a biological process can set disease in motion. But for many rare conditions, the course of progression remains unwritten. A groundbreaking natural history study led by researchers at Mayo Clinic's Center for Individualized Medicine and Department of Clinical Genomics aims to change that, advanci

Melbourne researchers have designed a world first test they hope will save the lives of thousands of children. The new procedure detects early stages of rare genetic disorders, so treatment can start before it is too late. 7NEWS at 6pm | More local news: www.7news.com.au/news/vic #7NEWS | 7NEWS Melbourne