Results 11 to 20 of about 697 (144)
BMC Nephrology, 2021 Background Acquired Gitelman syndrome is a very rare disorder reported in association with autoimmune disorders, mostly Sjögren syndrome. It is characterized by the presence of hypokalaemic metabolic alkalosis, hypocalciuria, hypomagnesaemia and hyper ...
Rasika Ranaweerage +2 more
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Bartter syndrome with long-term follow-up: a case report
Journal of International Medical Research, 2020 Bartter syndrome is a rare inherited disease caused by CLCNKB mutation, which results in inactivation of the chloride channel Kb protein. Bartter syndrome is characterized by extreme hypokalemia, hypochloremia, metabolic alkalosis, hyperrenin-induced ...
Xueling Wu +6 more
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Case Reports in Critical Care, 2015 Metabolic alkalosis secondary to citrate toxicity from plasma exchange is very uncommon in patients with normal renal function. In patients with advanced renal disease this can be a fatal event.
Mohsin Ijaz, Naeem Abbas, Dmitry Lvovsky
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Case Reports in Nephrology and Dialysis, 2018 A 23-year-old woman was referred to the tertiary centre with acute kidney injury and severe metabolic alkalosis following an accidental ethylene glycol poisoning.
Vojtěch Matoušek +3 more
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Bartter Syndrome Represented by Recurrent Hypokalemia Attacks: A Case Report
Southern Clinics of Istanbul Eurasia, 2017 Bartter syndrome is a tubular disorder and characterized with hypokalemia, hypokalemic metabolic alkalosis, hyperreninemia, normal blood pressure, increased loss of urinary sodium, potassium and chloride.
Nuran Küçük +4 more
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Metabolic alkalosis: pathogenesis and physiopathology
Emergency Care Journal, 2008 Metabolic alkalosis is an acid-base disorder frequently encountered in hospitalised patients, particularly those in critical conditions and is not infrequently complicated by mixed acid-base disorders. This disorder can have serious clinical consequences,
Mario Tarantino +2 more
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Bartter Type 4a Syndrome Diagnosed in a 30-week-old Preterm Neonate
Bagcilar Medical Bulletin, 2023 Bartter syndrome is an uncommon autosomal recessive, salt-losing renal tubular disease. Its defining features are numerous electrolyte abnormalities, including low potassium and chloride levels, metabolic alkalosis, and low or normal blood pressure.
Çağrı Cumhur Gök +4 more
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A mosaic mutation in the CLCNKB gene causing Bartter syndrome: A case report
Frontiers in Pediatrics, 2023 BackgroundType III Bartter syndrome (BS) is an autosomal recessive disease caused by mutations in the CLCNKB (chloride voltage-gated channel Kb) gene that encodes CLC-Kb.
Lan Zhou +7 more
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Severe Hypokalaemia, Hypertension, and Intestinal Perforation in Ectopic Adrenocorticotropic Hormone Syndrome [PDF]
Journal of Clinical and Diagnostic Research, 2016 Ectopic adrenocorticotropic hormone (ACTH) syndrome is a rare cause of the Cushing’s syndrome. The occurrence of the ectopic ACTH syndrome presenting with severe hypokalaemia, metabolic alkalosis, and hypertension has been highlighted in case reports ...
Tezcan Kaya +4 more
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The Journal of Association of Chest Physicians, 2016 The ectopic adrenocorticotropic hormone (ACTH) syndrome is an uncommon cause of hypercortisolism, which should be considered in patients with hypokalemic metabolic alkalosis and hypertension in the context of lung neoplasm.
Mansoor C Abdulla, Jemshad Alungal
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