Fabry disease results from GLA gene mutations, impairing alpha-galactosidase A enzyme production. This causes globotriaosylceramide to accumulate in organs, leading to symptoms such as pain, kidney failure, and cardiac issues.
| List - I | List – II | ||
| A. | Epinephrine | i. | Hyperglycemia |
| B. | Thyroxine | ii. | Smooth muscle contraction |
| C. | Oxytocin | iii. | Basal metabolic rate |
| D. | Glucagon | iv. | Emergency hormone |