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Fatty Acid Oxidation Disorders
- Glutaric Aciduria, Type 1
- Glycogen Storage Disease
- Homocystinuria
- Hyperphenylalaninemia and Phenylketonuria (PKU)
- Maternal Amino Acid Disorders
- Maternal Urea Cycle Disorders
- Mitochondrial Disease
- Organic Acid Disorders
- Overview, Current Research and Findings, Case Studies, Emerging Treatments and Nutrition Management of Phenylketonuria and Maternal Phenylketonuria
- Overview and Current Research and Findings, Case Studies, Emerging Treatments and Nutrition Management of Galactosemia
Educational Activity Learning Objectives
Upon completion of this activity, the participants should be able to:
- Describe the impact of elevated Phe on long-term patient outcomes
- Recognize the critical importance of therapeutic adherence and new treatment options available
- Discuss current therapeutic guidance in the treatment of PKU
- Explain the dietary implications of current and emerging treatment options