Синдром Барттера
ORPHA:112· ICD-10 E26.8· Bartter syndrome
Визначення(English summary)
Bartter syndrome is a group of rare renal tubular disease characterized by impaired salt reabsorption in the thick ascending limb of Henle's loop and clinically by the association of hypokalemic alkalosis, hypercalciuria/nephrocalcinosis, increased levels of plasma renin and aldosterone, low blood pressure and vascular resistance to angiotensin II.
- Поширеність
- Unknown
- Успадкування
- Autosomal dominant, Autosomal recessive, X-linked recessive
- Вік початку
- Adolescent, Adult, Antenatal, Childhood, Infancy, Neonatal