3-ketothiolase deficiency

Beta-ketothiolase deficiency is a rare, autosomal recessive metabolic disorder in which the body cannot properly process the amino acid isoleucine or the products of lipid breakdown.The typical age of onset for this disorder is between 6 months and 24 months. Symptoms and signs The signs and symptoms of beta-ketothiolase deficiency include vomiting, dehydration, trouble breathing, extreme tiredness, and occasionally convulsions. [Source: Wikipedia ]