Gordonov syndróm hyperkaliémie a hypertenzie hyperkaliémia a hypertenzia familiárna hyperkaliémia hypertenzívna familiárna pseudohypoaldosteronizmus, typ 1 pseudohypoaldosteronizmus, typ I pseudohypoaldosteronizmus typu 1, autozomálne recesívny pseudohypoaldosteronizmus typu I, autozomálne dominantný pseudohypoaldosteronizmus typu I, autozomálne recesívny pseudohypoaldosteronizmus typu II
English X references
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
Scope note in 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.
