Literature DB >> 8730418

Normal fibrinolytic responses to 1-desamino-8-D-arginine vasopressin in patients with nephrogenic diabetes insipidus caused by mutations in the aquaporin 2 gene.

A F van Lieburg1, V V Knoers, R Mallmann, W Proesmans, L P van den Heuvel, L A Monnens.   

Abstract

Three patients with autosomal-recessive nephrogenic diabetes insipidus (NDI), homozygous for mutations in the aquaporin 2 gene (AQP2), were tested for their fibrinolytic and hemodynamic responses to intravenous administration of 1-desamino-8-D-arginine vasopressin (DDAVP). They all showed an increase of tissue-type plasminogen activator antigen, facial flushing, an increase of heart rate and a decrease of diastolic blood pressure. These results confirm the hypothesis that NDI patients with an AQP2 defect can be discriminated from NDI patients with a vasopressin type 2 receptor defect by their normal extrarenal responses to DDAVP.

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Year:  1996        PMID: 8730418     DOI: 10.1159/000188936

Source DB:  PubMed          Journal:  Nephron        ISSN: 1660-8151            Impact factor:   2.847


  1 in total

1.  Two novel mutations in the aquaporin 2 gene in a girl with congenital nephrogenic diabetes insipidus.

Authors:  Hae Il Cheong; Su Jin Cho; Shou Huan Zheng; Hee Yeon Cho; Il Soo Ha; Yong Choi
Journal:  J Korean Med Sci       Date:  2005-12       Impact factor: 2.153

  1 in total

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