hereditary renal tubular defects

Etiology: 1) polycystic kidney disease a) adult b) infantile c) childhood 2) medullary sponge disease 3) medullary cystic disease a) recessive b) dominant 4) Bartter's syndrome 5) Liddle's syndrome 6) familial nephrogenic diabetes insipidus 7) renal tubular acidosis, type 1 8) renal tubular acidosis, type 2 9) X-linked hypophosphatemia 10) vitamin D-dependent rickets a) type 1 b) type 2 11) renal glycosuria 12) isolated hypouricemia 13) cystinuria 14) Hartnup disease 15) iminoglycinuria 16) adult Fanconi syndrome 17) Lowe's oculocerebrorenal syndrome

General

genetic disease of the kidney renal tubular disease

References

Harrison's Principles of Internal Medicine, 13th ed. Isselbacher et al (eds), McGraw-Hill Inc. NY, 1994, pg 1324