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MDDA | Metabolic Dietary Disorders Association
Phenylketonuria, PKU, Tyrosinaemia, TYRO, Maple Syrup Urine Disease, MSUD, Homocystinuria, HCU, Urea Cycle Disorders, USD, Ornithine Transcarbamylase Deficiency, OTC, Citrullinaemia, Argininosuccinic Acidaemia, ASA, Arginase Deficiency, ARG, Organic Acidaemias, Glutaric Acidaemia, GA1, GA2, Methylmalonic Aciduria, MMA, Propionic Acidaemia, PA, 3-Methylcrotonyl CoA Carboxylase Deficiency, 3MCC, Isovaleric Aciduria, IVA, Carbohydrate Metabolism, Galactosaemia, Glycogen Storage Disorders, Fructose
Metabolic Dietary Disorders Association (MDDA) is a national self-help group founded in 1996 by parents to support other families and individuals affected by Inborn Errors of Metabolism (IEMs). Rare genetic disorders including Phenylketonuria (PKU), Urea Cycle Disorders, Galactosaemia, Tyrosinaemia (TYRO). MDDA supports and represents families and individuals affected by a genetic Inborn Error of Metabolism whereby treatment involves a medically controlled diet.
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