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Utility of genetic testing in suspected familial cranial diabetes insipidus
AIM: Differentiating familial cranial diabetes insipidus (CDI) from primary polydipsia can be difficult. We report the diagnostic utility of genetic testing as a means of confirming or excluding this diagnosis. PATIENT AND METHODS: The index case presented at 3 months with polydipsia. He was diagnos...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioScientifica
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3922071/ https://ncbi.nlm.nih.gov/pubmed/24616780 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1530/EDM-13-0068 |
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