USMLE Step 1, 2 & 3 Pediatric Genetic Disorders, Inborn Errors of Metabolism, Part 1
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About USMLE Step 1, 2 & 3 Pediatric Genetic Disorders, Inborn Errors of Metabolism, Part 1
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USMLE Step 1, 2 & 3 Pediatric Genetic Disorders Review, Inborn Errors of Metabolism, Part 1. Your complete guide to inborn errors of metabolism for USMLE medical boards. High-Yield rapid review updated for 2025. Our live Zoom USMLE tutoring session is in a question and answer format so you can test yourself on the content. The session covers the critical details of inborn errors of metabolism including the basic science, pathology, pharmacology, diagnostic tests, and treatments required for Step 1, Pediatrics NBME clinical shelf exam, Step 2, Step 3, and ABP pediatrics boards. In this lecture, we discuss inborn errors of amino acid metabolism, carbohydrate metabolism, nucleotide synthesis, and the organic acidemias. In part 2, we discuss inborn errors of fatty acid metabolism, urea cycle disorders, lysosomal storage disorders, peroxisomal disorders, mitochondrial diseases, and disorders of pyruvate metabolism (pyruvate dehydrogenase and pyruvate carboxylase deficiencies). This is an important review of medical school biochemistry metabolic pathways and metabolic disorders. www.lectureboss.com [email protected] David Avarbock, MD, PhD
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