A Rare Case of Familial Neurogenic Diabetes Insipidus in a 22-Year-Old Man

A Rare Case of Familial Neurogenic Diabetes Insipidus in a 22-Year-Old Man

Objective: Diabetes insipidus (DI) can be classified into 2 types: central/neurogenic DI and nephrogenic DI. Most cases of central DI occur after brain surgery, trauma, tumor, or infection. Here we report a rare case of familial central DI due to a heterozygous AVP gene mutation. Methods: A case of...

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Auteurs principaux: Van T.T. Phan, MD, Zachary W. Bloomer, MD, Vien T.X. Phan, PhD, Mohamed K.M. Shakir, MD, Thanh D. Hoang, DO
Format: article
Langue:EN
Publié: Elsevier 2021
Sujets:
polyuria
polydipsia
central diabetes insipidus
familial diabetes insipidus
AVP gene
desmopressin
Diseases of the endocrine glands. Clinical endocrinology
RC648-665
Accès en ligne:https://doaj.org/article/97fcf741a46348a98e3b40d34ee5d073
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https://doaj.org/article/97fcf741a46348a98e3b40d34ee5d073

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