Genetic causes of hypomagnesemia, a clinical overview

Pediatric Nephrology

Volumn 32, Issue 7, 2017, Pages 1123-1135

  Viering, Daan H H M ^a,b   de Baaij, Jeroen H F ^b   Walsh, Stephen B ^a   Kleta, Robert ^a,c   Bockenhauer, Detlef ^a,c  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

^b RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^c GREAT ORMOND STREET HOSPITAL   (United Kingdom)

Author keywords

Distal convoluted tubule; Hereditary; Homeostasis; Kidney; Magnesium; Thick ascending limb of Henle s loop

Indexed keywords

ADENOSINE TRIPHOSPHATASE (POTASSIUM SODIUM); CALCIUM SENSING RECEPTOR; CHLORIDE CHANNEL; CHLORIDE CHANNEL KB; CLAUDIN; CLAUDIN 16; CLAUDIN 19; CNNM2 PROTEIN; FAM111A PROTEIN; FXYD2 PROTEIN; HEPATOCYTE NUCLEAR FACTOR 1BETA; INWARDLY RECTIFYING POTASSIUM CHANNEL; INWARDLY RECTIFYING POTASSIUM CHANNEL SUBUNIT KIR4.1; MAGNESIUM; PCBD1 PROTEIN; POTASSIUM CHANNEL KV1.1; SODIUM CHLORIDE COTRANSPORTER; TRANSIENT RECEPTOR POTENTIAL CHANNEL M6; UNCLASSIFIED DRUG; EPITHELIAL SODIUM CHANNEL BLOCKING AGENT; MEMBRANE PROTEIN; MINERALOCORTICOID ANTAGONIST;

ATAXIA; AUTOSOMAL DOMINANT DISORDER; AUTOSOMAL DOMINANT TUBULOINTERSTITIAL KIDNEY DISEASE; BARTTER SYNDROME; DIABETES MELLITUS; DISORDERS OF MITOCHONDRIAL FUNCTIONS; EPILEPSY; GAIN OF FUNCTION MUTATION; GENETIC DISORDER; GITELMAN SYNDROME; HEREDITY; HOMEOSTASIS; HUMAN; HYPERCALCIURIA; HYPOCALCEMIA; HYPOMAGNESEMIA; KIDNEY CALCIFICATION; KIDNEY CYST; KIDNEY DISEASE; KIDNEY TUBULE DISORDER; MITOCHONDRIAL HYPOMAGNESEMIA; NONHUMAN; PERCEPTION DEAFNESS; PHENOTYPE; PRIORITY JOURNAL; REVIEW; WASTING SYNDROME; BLOOD; CHILD; COMPLICATION; DIETARY REFERENCE INTAKE; DRUG EFFECTS; GENETICS; HEART ARRHYTHMIA; HENLE LOOP; HYPOKALEMIA; KIDNEY DISTAL TUBULE; KIDNEY TUBULE ABSORPTION; MAGNESIUM DEFICIENCY; METABOLISM; MITOCHONDRION; MUTATION; PHYSIOLOGY; SEIZURE; URINARY EXCRETION;

ARRHYTHMIAS, CARDIAC; CHILD; EPITHELIAL SODIUM CHANNEL BLOCKERS; HOMEOSTASIS; HUMANS; HYPERCALCIURIA; HYPOKALEMIA; KIDNEY TUBULES, DISTAL; LOOP OF HENLE; MAGNESIUM; MAGNESIUM DEFICIENCY; MEMBRANE PROTEINS; MINERALOCORTICOID RECEPTOR ANTAGONISTS; MITOCHONDRIA; MUTATION; NEPHROCALCINOSIS; PHENOTYPE; RECOMMENDED DIETARY ALLOWANCES; RENAL ELIMINATION; RENAL REABSORPTION; RENAL TUBULAR TRANSPORT, INBORN ERRORS; SEIZURES;

EID: 84970976574     PISSN: 0931041X     EISSN: 1432198X     Source Type: Journal    
DOI: 10.1007/s00467-016-3416-3     Document Type: Review

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