Last Day Revision

On this page 11 sections
MCQ Tips — Must Memorize
| MCQ clue | Answer |
|---|---|
| Night blindness | Vitamin A deficiency |
| Rickets / osteomalacia | Vitamin D deficiency |
| Hemolysis with neurologic dysfunction | Vitamin E deficiency |
| Prolonged PT due to defective clotting-factor carboxylation | Vitamin K deficiency |
| Wernicke–Korsakoff syndrome | Vitamin B1 deficiency |
| Pellagra: dermatitis, diarrhea, dementia | Vitamin B3 deficiency |
| Isoniazid-associated neuropathy | Vitamin B6 deficiency |
| Megaloblastic anemia with neurologic signs | Vitamin B12 deficiency |
| Bleeding gums and poor wound healing | Vitamin C deficiency |
| Catecholamine precursor | Tyrosine |
| Serotonin precursor | Tryptophan |
| GABA precursor | Glutamate |
| Nitric oxide precursor | Arginine |
| Collagen hydroxylation | Vitamin C |
| Collagen cross-linking | Lysyl oxidase; copper |
| Osteogenesis imperfecta | Type I collagen |
| Cartilage collagen | Type II |
| Basement membrane collagen | Type IV |
| Von Gierke disease | Glucose-6-phosphatase system |
| Pompe disease | Lysosomal acid α-glucosidase |
| Cori disease | Debranching enzyme |
| Andersen disease | Branching enzyme |
| McArdle disease | Muscle glycogen phosphorylase |
| Rate-limiting enzyme of glycolysis | PFK-1 |
| TCA enzyme also Complex II | Succinate dehydrogenase |
| Final electron acceptor in ETC | Oxygen |
| Tay–Sachs disease | Hexosaminidase A deficiency |
| Gaucher disease | β-Glucocerebrosidase deficiency |
| Niemann–Pick A/B | Acid sphingomyelinase deficiency |
| Highest triglyceride transport from intestine | Chylomicrons |
| Main atherogenic cholesterol carrier | LDL |
| ApoC-II | Activates LPL |
| ApoB-48 | Chylomicrons |
| ApoB-100 | VLDL, IDL and LDL; LDL-receptor binding |
| ApoA-I | Activates LCAT |
| HMG-CoA reductase | Rate-limiting cholesterol synthesis enzyme |
| Competitive inhibition | Km increases; Vmax unchanged |
| Pure noncompetitive inhibition | Vmax decreases; Km unchanged |
| Fat energy yield | 9 kcal/g |
| Carbohydrate energy yield | 4 kcal/g |
| Protein energy yield | 4 kcal/g |
| Refeeding syndrome | Hypophosphatemia is a key clue |
Vitamin Deficiencies
A
A — Eyes and epithelium
Night blindness, xerophthalmia, Bitot spots.
B1
Thiamine — Energy metabolism
Beriberi, Wernicke–Korsakoff; TPP-dependent enzymes.
B3
Niacin — Pellagra
Dermatitis, diarrhea, dementia.
B6
Pyridoxine — PLP
Neuropathy, seizures, sideroblastic anemia; isoniazid association.
B9
Folate — DNA synthesis
Megaloblastic anemia, increased homocysteine, normal methylmalonic acid.
B12
Cobalamin — Blood and nerves
Megaloblastic anemia, neurologic dysfunction, increased homocysteine and methylmalonic acid.
C
Ascorbic acid — Collagen
Scurvy, bleeding gums, perifollicular hemorrhage, poor healing.
Classic Contrasts
| Contrast | Key distinction |
|---|---|
| Folate vs B12 | Both cause megaloblastic anemia; B12 can cause neurologic dysfunction |
| Type I vs Type II collagen | Type I: bone/dentin; Type II: cartilage |
| Von Gierke vs McArdle | Severe fasting hypoglycemia vs exercise-induced muscle symptoms |
| Pompe vs other classic GSDs | Lysosomal glycogen accumulation with cardiomyopathy |
| Tay–Sachs vs Niemann–Pick | Hepatosplenomegaly is typically absent in Tay–Sachs but common in Niemann–Pick |
| Glycolysis vs TCA | Cytoplasm vs mitochondrial matrix |
| PFK-1 vs pyruvate kinase | PFK-1 is the major rate-limiting step; pyruvate kinase catalyzes the final ATP-generating step |
| Chylomicrons vs VLDL | Dietary triglycerides vs liver-derived triglycerides |
| LDL vs HDL | Cholesterol delivery to tissues vs reverse cholesterol transport |
| ApoC-II vs ApoE | LPL activation vs remnant uptake |
| Competitive vs noncompetitive inhibition | Increased Km vs reduced Vmax in pure noncompetitive inhibition |
Energy metabolism
| Pathway | Key yield |
|---|---|
| Glycolysis per glucose | Net 2 ATP + 2 NADH + 2 pyruvate |
| TCA per acetyl-CoA | 3 NADH + 1 FADH₂ + 1 GTP + 2 CO₂ |
| NADH | Approximately 2.5 ATP |
| FADH₂ | Approximately 1.5 ATP |
| Complete glucose oxidation | Approximately 30–32 ATP |