• Thumbnail for Bartter syndrome
    Bartter syndrome (BS) is a rare inherited disease characterised by a defect in the thick ascending limb of the loop of Henle, which results in low potassium...
    16 KB (1,686 words) - 22:44, 28 February 2023
  • inappropriate antidiuretic hormone (SIADH) in 1957 and Bartter syndrome in 1963. Schwartz-Bartter syndrome is named after these two scientists. The first reports...
    35 KB (4,047 words) - 04:10, 27 May 2024
  • Thumbnail for Gitelman syndrome
    pharmacological inhibition of NCC activity). Gitelman syndrome was formerly considered a subset of Bartter syndrome until the distinct genetic and molecular bases...
    28 KB (2,941 words) - 23:36, 2 May 2024
  • Bart syndrome Bartter syndrome Bart–Pumphrey syndrome Bassen-Kornzweig syndrome Battered person syndrome Bazex–Dupré–Christol syndrome Beare–Stevenson...
    41 KB (4,052 words) - 14:58, 17 June 2024
  • Thumbnail for Polyhydramnios
    Bartter-like syndromes". Nat Clin Pract Nephrol. 4 (10): 560–7. doi:10.1038/ncpneph0912. PMID 18695706. S2CID 205340294. "Hereditary disease: Bartter...
    8 KB (872 words) - 15:37, 8 March 2024
  • Thumbnail for BSND
    Bartter syndrome, infantile, with sensorineural deafness (Barttin), also known as BSND, is a human gene which is associated with Bartter syndrome. This...
    5 KB (593 words) - 04:38, 9 January 2024
  • Thumbnail for Hypokalemia
    society. Bartter syndrome Gitelman syndrome Hypokalemic acidosis Potassium deficiency (plant disorder) Superior mesenteric artery syndrome Soar J, Perkins...
    34 KB (3,617 words) - 21:34, 16 March 2024
  • Factitious disorder imposed on self, also known as Munchausen syndrome, is a factitious disorder in which those affected feign or induce disease, illness...
    28 KB (2,997 words) - 15:25, 4 July 2024
  • Thumbnail for Exome sequencing
    successful clinical diagnosis of a suspected Bartter syndrome patient of Turkish origin. Bartter syndrome is a renal salt-wasting disease. Exome sequencing...
    41 KB (4,675 words) - 08:58, 18 March 2024
  • inappropriate antidiuretic hormone (SIADH) in 1957 and Bartter syndrome in 1963. Schwartz-Bartter syndrome is named after these two scientists. The first reports...
    25 KB (2,849 words) - 19:05, 21 June 2024
  • Thumbnail for Tetany
    needed] Metabolic alkalosis with hypokalemia like Gitelman syndrome and Bartter syndrome can cause tetany. Vomiting induced alkalosis and hyperventilation...
    8 KB (833 words) - 04:15, 27 May 2024
  • Thumbnail for Hyperaldosteronism
    potassium wasting. These conditions can be referred to syndromes such as Bartter syndrome and Gitelman syndrome. Pseudohyperaldosteronism mimicks hyperaldosteronism...
    9 KB (861 words) - 19:26, 8 July 2024
  • Thumbnail for CLCNKB
    termini. Mutations in CLCNKB result in the autosomal recessive Type III Bartter syndrome. CLCNKA and CLCNKB are closely related (94% sequence identity), tightly...
    9 KB (1,146 words) - 00:50, 17 July 2024
  • affecting the kidney and his discovery of syndrome of inappropriate antidiuretic hormone and Bartter syndrome. He had a separate interest in mushroom poisoning...
    7 KB (669 words) - 17:33, 10 June 2023
  • Thumbnail for Nephrocalcinosis
    hypercalcemia, medullary nephrocalcinosis of any cause, or in children with Bartter syndrome in whom essential tubular salt reabsorption is compromised. There are...
    15 KB (1,574 words) - 03:40, 17 September 2023
  • Thumbnail for Metabolic alkalosis
    blood Severely high levels of calcium in the blood Bartter syndrome and Gitelman syndromesyndromes with presentations analogous to taking diuretics characterized...
    11 KB (1,225 words) - 11:43, 13 March 2024
  • develop more targeted and personalized interventions. For example, Bartter Syndrome, also known as salt-wasting nephropathy, is a hereditary disease of...
    17 KB (1,904 words) - 20:14, 9 March 2024
  • disease Bartter syndrome Diuretic phase of acute tubular necrosis Some diuretics Primary renal diseases Congenital adrenal hyperplasia Syndrome of inappropriate...
    2 KB (266 words) - 02:19, 17 March 2023
  • Barnicoat–Baraitser syndrome Barrett syndrome Barrow–Fitzsimmons syndrome Barth syndrome Bartonella infections Bartsocas–Papas syndrome Bartter syndrome, antenatal...
    12 KB (1,033 words) - 01:07, 12 June 2024
  • Thumbnail for Generalized glucocorticoid resistance
    Generalized glucocorticoid resistance or Chrousos syndrome is a rare genetic disorder that can run in families or be sporadic. It is characterized by partial...
    17 KB (1,476 words) - 07:39, 3 June 2024
  • degree Bernard–Soulier syndrome, a rare autosomal recessive coagulopathy, that is caused a deficiency of glycoprotein Ib Bartter syndrome, a rare inherited...
    5 KB (626 words) - 22:00, 22 June 2024
  • sickle cell disease or trait, amyloidosis, Sjögren syndrome, renal cystic disease, Bartter syndrome, and various medications (amphotericin B, orlistat...
    11 KB (1,189 words) - 07:57, 2 July 2024
  • Encapsulating peritoneal sclerosis (EPS) is a chronic clinical syndrome with an insidious onset that manifests as chronic undernourishment accompanied...
    52 KB (4,970 words) - 08:16, 28 January 2024
  • – Caspar Bartholin Bartter syndrome – Frederic Bartter Basedow coma – Karl Adolph von Basedow Basedow disease (aka Basedow syndrome, Begbie disease, Flajan...
    62 KB (6,514 words) - 09:17, 9 July 2024
  • Thumbnail for Spastic ataxia-corneal dystrophy syndrome
    member of the family who was first diagnosed with this disease also had Bartter syndrome. It was concluded by its first descriptors Mousa-Al et al. that the...
    3 KB (215 words) - 08:36, 30 September 2020
  • Thumbnail for Channelopathy
    cardiac channelopathies make up a key group of heart diseases. Long QT syndrome, the most common form of cardiac channelopathy, is characterized by prolonged...
    14 KB (1,120 words) - 03:33, 20 May 2024
  • help EAST syndrome as a whole, but hopefully with continued research, there could be one day.[citation needed] Gitelman syndrome Bartter syndrome Liddle's...
    14 KB (1,611 words) - 06:57, 26 July 2023
  • Bart–Pumphrey syndrome; 149200; GJB2 Bartter syndrome, type 1; 601678; SLC12A1 Bartter syndrome, type 2; 241200; KCNJ1 Bartter syndrome, type 3; 607364;...
    234 KB (18,877 words) - 15:43, 9 May 2024
  • Thumbnail for ROMK
    sialic acid. Mutations in this gene have been associated with antenatal Bartter syndrome, which is characterized by salt wasting, hypokalemic alkalosis, hypercalciuria...
    14 KB (1,756 words) - 10:15, 6 January 2024
  • and 15, respectively. A loss of function mutation of NKCC2 produces Bartter syndrome, an autosomal recessive disorder characterized by hypokalemic metabolic...
    13 KB (1,671 words) - 14:29, 11 July 2024