| Literature DB >> 23409988 |
Yoko Shida1, Hisafumi Matsuoka, Motoko Chiga, Shinichi Uchida, Sei Sasaki, Shigetaka Sugihara.
Abstract
We identified the AQP-2 gene mutation (R254Q) in a family with dominant NDI. The patient studied here has NDI with partial response to the anti-diuretic effect of AVP and dDAVP. Hereditary NDI seems to have the uniform clinical manifestations, but this might only reflect the information on screened patients with clear clinical presentations. It may be that a milder form of NDI has been overlooked due to a lack of genetic identification. Gene mutation analysis should be considered even in patients with mild NDI symptoms. Fortunately, both V2R and AQP2 genes are small and can be easily analyzed.Entities:
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Year: 2013 PMID: 23409988 DOI: 10.1111/j.1442-200X.2012.03614.x
Source DB: PubMed Journal: Pediatr Int ISSN: 1328-8067 Impact factor: 1.524