Hyponatremia resulting from Arginine Vasopressin Receptor 2 gene mutation

Pediatric Nephrology

Volumn 22, Issue 3, 2007, Pages 463-466

  Bes, David Francisco ^a   Mendilaharzu, Herná ^a   Fenwick, Raymond G ^b   Arrizurieta, Elvira ^c  

^a HOSPITAL DE PEDIATRÍA PROF DR JUAN P GARRAHAN   (Argentina)

^b QUEST DIAGNOSTICS NICHOLS INSTITUTE   (United States)

^c INSTITUTO DE INVESTIGACIONES MÉDICAS ALFREDO LANARI   (Argentina)

Author keywords

AVPR2; Hypo osmolarity syndrome of inappropriate antidiuresis; Nephrogenic syndrome of inappropriate antidiuresis; Seizure; Syndrome of inappropriate secretion of antidiuretic hormone; Water excretion

Indexed keywords

ALBUMIN; ARGIPRESSIN RECEPTOR; ARGIPRESSIN RECEPTOR 2; BICARBONATE; CHLORIDE; POTASSIUM; SODIUM; SODIUM CHLORIDE; UNCLASSIFIED DRUG; UREA; VASOPRESSIN;

ARTICLE; CARBON DIOXIDE TENSION; CASE REPORT; CHRONIC DISEASE; CODON; CONGENITAL NEPHROTIC SYNDROME; DIABETES INSIPIDUS; DNA SEQUENCE; FLUID INTAKE; GENE MUTATION; HOSPITAL ADMISSION; HUMAN; HYPONATREMIA; INAPPROPRIATE VASOPRESSIN SECRETION; MALE; OXYGEN TENSION; PH; PRIORITY JOURNAL; PROTEIN BLOOD LEVEL; SCHOOL CHILD; SEIZURE; SERUM OSMOLALITY; SODIUM BLOOD LEVEL; URINE OSMOLALITY; VASOPRESSIN RELEASE; VENOUS BLOOD; WHEEZING;

CHRONIC DISEASE; DIAGNOSIS, DIFFERENTIAL; EXTRACELLULAR FLUID; HUMANS; HYPONATREMIA; INAPPROPRIATE ADH SYNDROME; INFANT; MALE; MUTATION; RECEPTORS, VASOPRESSIN; SODIUM;

EID: 34248648457     PISSN: 0931041X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00467-006-0344-7     Document Type: Article

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