Fabry disease is caused by mutations in the GLA gene, which codes for the alpha-galactosidase A enzyme. This leads to the accumulation of globotriaosylceramide in various organs, causing symptoms such as pain, kidney failure, and cardiac issues.
| List I | Condition/Structure | List II Description |
|---|---|---|
| A | Hypokalemia | IV. Potassium |
| B | Hypocapnia | II. CO2 |
| C | Sudoriferous glands | I. Sweat glands |
| D | Sertoli cells | III. Spermatogenesis |