A young boy suffering from a condition described as a combination of and Pakinson's is hoping for a miracle after clinical trials for a drug to treat his condition were cut short - leaving him reeling.Leo Vauclare, 6, is suffering from infantile neuroaxonal dystrophy (INAD), a condition caused by a missing enzymes in a person's body or a dangerous build up on iron. He was diagnosed at age two.The rare diagnosis only affects around 150 children worldwide, Vauclare's parents told , and its rarity also means that there are little options for treatment available.
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