Abstract |
Diabetes insipidus (DI) is characterized by hypoosmotic polyuria related to deficiency of arginine-vasopressin (AVP) secretion (centraldiabetesinsipidus, CDI) or renalinsensitivity to AVP (nephrogenicdiabetesinsipidus, NDI). We report a case of a child with congenital NDI.
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Authors | A Sallemi, G Stroscio, D Impollonia, T Arrigo, V Di Benedetto, V Salvo, L Marseglia, M G Scuderi, M P Calabrò, C Fede, C Cuppari, C Salpietro, R Chimenz |
Journal | Journal of biological regulators and homeostatic agents
(J Biol Regul Homeost Agents)
2019 Sep-Oct
Vol. 33
Issue 5 Suppl. 1
Pg. 3-5. Special Issue: Focus on Pediatric Nephrology
ISSN: 0393-974X [Print] Italy |
PMID | 31630706
(Publication Type: Case Reports, Journal Article)
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Copyright | Copyright 2019 Biolife Sas. www.biolifesas.org. |
Chemical References |
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Topics |
- Child
- Diabetes Insipidus, Nephrogenic
(congenital)
- Electrolytes
(analysis)
- Failure to Thrive
- Humans
- Polyuria
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