hereditary renal tubular defects
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Etiology
- polycystic kidney disease
- adult
- infantile
- childhood
- medullary sponge disease
- medullary cystic disease
- recessive
- dominant
- metabolic alkalosis
- Gordon syndrome (hyperkalemia, hypertension, metabolic acidosis)
- familial nephrogenic diabetes insipidus
- renal tubular acidosis, type 1
- renal tubular acidosis, type 2
- X-linked hypophosphatemia
- vitamin D-dependent rickets
- type 1
- type 2
- renal glycosuria
- isolated hypouricemia
- cystinuria
- Hartnup disease
- iminoglycinuria
- adult Fanconi syndrome
- Lowe's oculocerebrorenal syndrome
More general terms
References
- ↑ Harrison's Principles of Internal Medicine, 13th ed. Isselbacher et al (eds), McGraw-Hill Inc. NY, 1994, pg 1324
- ↑ 2.0 2.1 Medical Knowledge Self Assessment Program (MKSAP) 20 American College of Physicians, Philadelphia 2025
- ↑ Guo W, Ji P, Xie Y. Genetic diagnosis and treatment of hereditary renal tubular disease with hypokalemia and alkalosis. J Nephrol. 2023;36:575-91. PMID: https://pubmed.ncbi.nlm.nih.gov/35994232