In the first years thyroid disease diarrhea

Treatment is by oral diarrhea thyroid disease

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In the first years of life this diarrhea deficiency will become apparent following a prolonged fasting period. Symptoms include vomiting, lethargy diarrhea and frequently coma. Excessive urinary excretion of medium-chain dicarboxylic acids as well as their glycine and carnitine esters is diagnostic of this condition. In the case of this enzyme deficiency. taking care to avoid prolonged fasting is sufficient to prevent clinical problems. 4. Refsum's Disease: Refsum's disease is a rare inherited disorder in which patients lack the mitochondrial a-oxidizing enzyme. As a consequence, they accumulate large quantities of phytanic acid in their tissues and serum. This leads diarrhea to severe symptoms, including cerebellar ataxia, retinitis pigmentosa, nerve deafness and peripheral neuropathy.

Treatment is by oral carnitine administration. 2. Carnitine Palmitoyltransferase I (CPT I) Deficiency: Deficiencies in this enzyme affect primarily the liver and lead thyroid disease to reduced fatty acid thyroid disease oxidation and ketogenesis. Carnitine Palmitoylransferase II (CPT II) deficiency results in recurrent muscle pain and fatigue and myoglobinuria following strenuous exercise. Carnitine acyltransferases may also be inhibited by sulfonylurea drugs such as tolbutamide and glyburide. 3. Deficiencies in Acyl-CoA Dehydrogenases: A group of inherited diseases that impair b-oxidation result from deficiencies thyroid disease in acyl-CoA dehydrogenases. The enzymes affected may belong to one of four categories: very long-chain acyl-CoA dehydrogenase (VLCAD) Disease description long-chain acyl-CoA dehydrogenase (LCAD)Disease description medium-chain acyl-CoA dehydrogenase (MCAD) Disease description short-chain acyl-CoA dehydrogenase (SCAD) Disease description MCAD deficiency is the most common form of this disease.

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