A Mutation in the Vasopressin V2-Receptor Gene in a Kindred with X-Linked Nephrogenic Diabetes Insipidus

John J. Merendino, Allen M. Spiegel, John D. Crawford, Anne Marie O'carroll, Michael J. Brownstein, Stephen J. Lolait

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Abstract

Hereditary nephrogenic diabetes insipidus is a rare, X-linked disorder manifested by an inability to concentrate the urine despite high plasma concentrations of arginine vasopressin or the administration of large doses of vasopressin or its analogues1,2. Affected males have profound hyposmotic polyuria soon after birth, often leading to recurrent episodes of severe dehydration. Unless recognized and treated early, these episodes may lead to failure to thrive, growth retardation, repeated bouts of cerebral edema with resultant mental retardation, or death. Females who are carriers of the gene for the disease have symptoms that range from a defective urinary-concentrating ability demonstrable…

Original languageEnglish (US)
Pages (from-to)1538-1541
Number of pages4
JournalNew England Journal of Medicine
Volume328
Issue number21
DOIs
Publication statusPublished - May 27 1993
Externally publishedYes

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ASJC Scopus subject areas

  • Medicine(all)

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