C0004775 - A group of disorders caused by defective salt reabsorption in the ascending LOOP OF HENLE. It is characterized by severe salt-wasting, HYPOKALEMIA; HYPERCALCIURIA; metabolic ALKALOSIS, and hyper-reninemic HYPERALDOSTERONISM without HYPERTENSION. There are several subtypes including ones due to mutations in the renal specific SODIUM-POTASSIUM-CHLORIDE SYMPORTERS.

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Lang Dictionary CODE			LUI	preferred no	SUI	preference Yes / No	Terms, descriptions
							CUI C0004775

Russian	Medical Subject Headings Russian	D001477	L5340878	preferred	S6102883	Y	БАРТЕРА СИНДРОМ
Russian	Medical Subject Headings Russian	D001477	L0890857	no	S1094674	Y	BARTERA BOLEZN'
Russian	MDRRUS	10050839	L16135593	no	S19408940	N	Синдром Бартера
Russian	MDRRUS	10050839	L16135593	no	S19408940	Y	Синдром Бартера
Russian	Medical Subject Headings Russian	D001477	L3340371	no	S3867852	Y	БАРТЕРА БОЛЕЗНЬ
Russian	Medical Subject Headings Russian	D001477	L6965471	no	S8105255	Y	BARTERA SINDROM
	(CPTSP) CRISP Thesaurus				A0318100	AT51219111	transmitted as an autosomal recessive trait; characterized by hypertrophy and hyperplasia of the juxtaglomerular cells, and increased concentrations of renin, angiotensin II, and aldosterone in the absence of edema and hypertension.
	Medical Subject Headings Czech				A13040719	AT231365858	Syndrom charakterizovaný hypokalemií, hypochloremickou alkalózou, zvýšenou plasmatickou reninovou aktivitou a koncentrací aldosteronu. Je zvýšena syntéza a vylučování prostaglandinů a kallikrein-kininového systému (není hypertenze). Dědičnost je autozomálně recesivní. Je porušena resorpce iontů ve vzestupném raménku Henleovy kličky (defekt iontových kanálů) s příslušnými kompenzačními změnami a hyperplazií juxtaglomerulárního aparátu. Klinické příznaky vycházejí z popsaných změn (zejm. výrazná slabost při hypokalemii a sklonu k hypotonii a hypovolemii), bývá rovněž narušen růst. Někdy dochází k poklesu renálních funkcí. (cit. Velký lékařský slovník online, 2017 http://lekarske.slovniky.cz/)
	NCI Thesaurus				A15560892	AT198103543	A rare inherited syndrome characterized by juxtaglomerular cell hyperplasia, hyperaldosteronism, hypokalemia, and alkalosis. Patients have high levels of plasma renin concentration which is not associated with hypertension.
	NCI National Institute of Child Health and Human Development				A15560892	AT210377570	A rare, inherited syndrome characterized by juxtaglomerular cell hyperplasia, hyperaldosteronism, hypokalemia, and alkalosis. Affected individuals have high concentration of plasma renin that is not associated with hypertension.
	(JABL) Congenital Mental Retardation Syndromes				A1702986	AT14332084	Hypertrophy and hyperplasia of the juxtaglomerular apparatus with secondary hyperaldosteronism with normal blood pressure and hyperkalemic alkalosis in the absence of edema. Most patients show growth and mental retardation. Nephrocalcinosis and hypercalcinuria occur in some cases. Diuretic abuse may produce a syndrome with similar characteristics (pseudo-Bartter or factitious Bartter syndrome).
	Medical Subject Headings				A6963975	AT115063268	A group of disorders caused by defective salt reabsorption in the ascending LOOP OF HENLE. It is characterized by severe salt-wasting, HYPOKALEMIA; HYPERCALCIURIA; metabolic ALKALOSIS, and hyper-reninemic HYPERALDOSTERONISM without HYPERTENSION. There are several subtypes including ones due to mutations in the renal specific SODIUM-POTASSIUM-CHLORIDE SYMPORTERS.