Gaucher’s disease is caused by a mutation in the gene encoding glucocerebrosidase, leading to the accumulation of glucocerebroside in cells, particularly macrophages, and resulting in symptoms such as hepatomegaly and bone pain.
| 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 |