Day 3: Biochemistry Lecture Part 1 Copy


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Biochemistry Rapid Course:

  1. Kartagener Syndrome
  2. Collagen Synthesis and Structure - Osteogenesis Imperfecta and Ehlers-Danlos Syndrome, Menkes Disease Elastin and Marfan Syndrome
  3. McCune-Albright Syndrome
  4. Important Genetic Disorders: Cystic Fibrosis and Rett Syndrome
  5. Trinucleotide Repeat Expansion Diseases: Huntington Disease, Myotonic Dystrophy, Fragile X syndrome and Friedreich Ataxia
  6. Autosomal Trisomies: Down syndrome, Edwards syndrome, Patau Syndrome
  7. Vitamin Deficiencies: ADEK, Vitamin B – B1 to B12 deficiency, Vitamin C Deficiency
  8. Ethanol metabolism, fomepizole, and disulfiram
  9. Essential Fructosuria and Hereditary Fructose Intolerance, and Galactokinase Deficiency and Classic Galactosemia
  10. Lactase Deficiency
  11. Hyperammonemia
  12. Urea Cycle and Ornithine transcarbamylase deficiency
  13. Pyruvate Errors of Metabolism
  14. Glycolysis
  15. TCA Cycle
  16. Gluconeogenesis
  17. G6PD Deficiency
  18. Catecholamine Synthesis/ Tyrosine Catabolism Diseases: Phenylketonuria, Maple Syrup Urine Disease, Alkaptonuria, Homocystinuria, and Cystinuria
  19. Gylcogen Storage Diseases: Von Glerke Disease, Pompe Disease, Cort Disease, McArdie disease
  20. Lysosomal Storage Diseases
  21. Fasting, and Starvation
  22. Lipoprotein Functions and Lipid Transfer
  23. Type I hyperchylomicronemia, type 2 familial hypercholesterolemia, type 3 dysbetalipoproteinemia, type 4 hyper-triglyceridemia