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