Create issue ticket

422 Possible Causes for Gitelman Syndrome

  • Gitelman Syndrome

    Genetic counseling is available for families affected by Gitelman syndrome.[] In contrast to people with Gordon's syndrome, those affected by Gitelman syndrome generally have low or normal blood pressure.[] Gitelman syndrome is an inherited tubulopathy that must be considered in some settings of hypokalaemia.[]

  • Metabolic Alkalosis

    Symptoms and renal outcomes of Gitelman's syndrome are, in general, mild and benign, and renal insufficiency from Gitelman's syndrome associated with long-standing hypokalemia[] Two patients had Bartter's syndrome and one patients had Gitelman's syndrome.[] Gitelman's syndrome is caused by the loss of funcion of the SLC12A3 gene and may resemble Bartter's syndrome, though is associated with the very low urinary calcium.[]

  • Eczema

    BACKGROUND: Loss-of-function mutations in the filaggrin (FLG) gene were identified as a major risk factor for atopic eczema. OBJECTIVES: The aim of the study was to investigate the importance of 4 common FLG null mutations in the susceptibility to atopic eczema and other allergic phenotypes in Polish children[…][]

  • Hypomagnesemia

    Gitelman syndrome (GS), an inherited disorder due to loss of function mutations of the gene encoding the distal convoluted tubule Na-Cl cotransporter (NCCT), is characterized[] We report a case of a woman with Gitelman syndrome who presented to our hospital mainly due to hyperemesis.[] The patient was ultimately diagnosed with Gitelman syndrome comorbid with schizophreniform disorder and avoidant restrictive food intake disorder.[]

  • Hypokalemia

    In general, the long-term prognosis of Gitelman's syndrome is good if the patient adhere with the treatment.[] syndrome.[] We describe a 79-year-old man with biochemical and radiological features of Gitelman syndrome: hypokalemia, hypomagnesemia, hyperreninemic hyperaldosteronism in absence of[]

  • Bartter's Disease

    […] three separate clinical entities – classic Bartter syndrome, antenatal Bartter syndrome and Gitelman syndrome.[] syndrome and low in Gitelman syndrome.[] Gitelman and Bartter Syndromes can be diagnosed by a DNA test. This is a simple blood test, which looks at the genes that cause the condition.[]

  • Alkalosis

    ’s syndrome and Bartter’s syndrome) undergoing non-urgent surgical procedures[] Hypomagnesaemia is seen in Gitelman's syndrome. 12-lead ECG - half of Gitelman's syndrome patients have prolonged QT interval.[] Clinical and Genetic Spectrum of Bartter Syndrome Type 3. J Am Soc Nephrol. 2017;28:2540-2552. Iqbal Z, Sayer JA. Chondrocalcinosis and Gitelman syndrome.[]

  • Autosomal Dominant Primary Hypomagnesemia with Hypocalciuria

    Differential diagnosis Differential diagnosis includes all causes of renal hypomagnesemia, particularly diseases associated with hypocalciuria such as Gitelman syndrome, EAST[] Box 9101, 6500 HB Nijmegen, The Netherlands. Source MeSH Gitelman Syndrome Humans Hypocalcemia Kidney Kidney Tubules Magnesium Magnesium Deficiency[] Bartter's syndrome causes hypocalcaemia, but Gitelman's syndrome causes hypercalcaemia.[]

  • Liddle Syndrome

    syndrome Much more common than Bartter syndrome Loss of function of NCCT (mutation in SCL12A3), hence resembles effect of thiazides Hypokalaemia, hypocalciuria and hypomagnesaemia[] NSAIDs reduce the polyuria and salt wasting in Bartter’s syndrome but are ineffective in Gitelman’s syndrome. They may be lifesaving in hyper prostaglandin E syndrome.[] Bartters, Gitelmans and Liddles syndrome present with chloride resistant (high urinary chloride) hypokalemic metabolic alkalosis.[]

  • Hypertension

    The patient was diagnosed as having primary hypertension with Gitelman syndrome (GS).[]

Further symptoms