Is renal tubular acidosis hereditary?

summary

Last week, my little daughter had renal tubular acidosis, but we didn't find it. When we took her to a small clinic for examination, the doctor didn't find it. Later, when we took her to a large hospital for examination, it was renal tubular acidosis. Later, the doctor told us about the basis of diagnosis and differentiation. Here I want to share with you, I sincerely hope that this situation like my little daughter will not happen to anyone again!

Is renal tubular acidosis hereditary?

1. The diagnosis of renal tubular acidosis is mainly based on four points: 1. Polyuria, polydipsia and polydipsia, except diabetes and diabetes insipidus.

2. 2. Bone and muscle pain. Metabolic (hyperchlorinated) acidosis, azotemia (or mild)

3. There are potassium, sodium, calcium and other electrolyte disorders (common hypokalemia or hyperkalemia, hyponatremia, hypocalcemia), unexplained double kidney stones and renal calcification.

matters needing attention

Treatment principle 1. Correct metabolic acidosis. 2. Correct the disorder of water and electrolyte. 3. Treatment of primary diseases. 4. Treatment of complications. 5. Hemodialysis is feasible when hyperkalemia is serious and obvious. 6. Symptomatic support therapy.