1 / 1
|
DeCS
|
|
|
Descriptor English:
|
|
Pseudohypoaldosteronism
|
Descriptor Spanish:
|
|
Seudohipoaldosteronismo
|
Descriptor Portuguese:
|
|
Pseudo-Hipoaldosteronismo
|
Synonyms English:
|
|
Gordon Hyperkalemia-Hypertension Syndrome
Hyperpotassemia and Hypertension, Familial
Hypertensive Hyperkalemia, Familial
Pseudohypoaldosteronism Type 1
Pseudohypoaldosteronism Type 1, Autosomal Recessive
Pseudohypoaldosteronism, Type I
Pseudohypoaldosteronism, Type I, Autosomal Dominant
Pseudohypoaldosteronism, Type I, Autosomal Recessive
Pseudohypoaldosteronism, Type II
|
Tree Number:
|
|
C12.777.419.815.770
C13.351.968.419.815.770
C16.320.565.861.770
C18.452.648.861.770
|
Definition English:
|
|
A heterogeneous group of disorders characterized by renal electrolyte transport dysfunctions. Congenital forms are rare autosomal disorders characterized by neonatal hypertension, HYPERKALEMIA, increased RENIN activity and ALDOSTERONE concentration. The Type I features HYPERKALEMIA with sodium wasting; Type II, HYPERKALEMIA without sodium wasting. Pseudohypoaldosteronism can be the result of a defective renal electrolyte transport protein or acquired after KIDNEY TRANSPLANTATION. |
See Related English:
|
|
Epithelial Sodium Channel
Receptors, Mineralocorticoid
|
History Note English:
|
|
1991(1988); use RENAL TUBULAR TRANSPORT, INBORN ERRORS 1988-90
|
Allowable Qualifiers English:
|
|
|
Record Number:
|
|
22975
|
Unique Identifier:
|
|
D011546
|
Occurrence in VHL:
|
|
|
Similar:
|
|
DeCS CID-10 SciELO LILACS LIS
|