A case of central diabetes insipidus due to neurophysin II gene abnormality diagnosed based on a family history of nocturnal enuresis.

Sugawara, Lucia; Nakamura, Takaaki; Ishizuka, Yoshitaka; Maegawa, Hiroshi

Sugawara, Lucia; Nakamura, Takaaki; Ishizuka, Yoshitaka; Maegawa, Hiroshi.

Sugawara L; Department of Endocrinology and Metabolism, Omihachiman Community Medical Center, Omihachiman, Shiga 523-0082, Japan.
Nakamura T; Department of Medicine, Shiga University of Medical Science, Otsu, Shiga 520-2092, Japan.
Ishizuka Y; Department of Endocrinology and Metabolism, Omihachiman Community Medical Center, Omihachiman, Shiga 523-0082, Japan.
Maegawa H; Department of Endocrinology and Metabolism, Omihachiman Community Medical Center, Omihachiman, Shiga 523-0082, Japan.

Endocr J ; 69(1): 95-100, 2022 Jan 28.

Article en En | MEDLINE | ID: mdl-34544934

Asunto(s)

Diabetes Insípida Neurogénica; Diabetes Mellitus; Enuresis Nocturna; Adulto; Arginina Vasopresina; Niño; Diabetes Insípida Neurogénica/diagnóstico; Diabetes Insípida Neurogénica/genética; Femenino; Humanos; Masculino; Mutación; Neurofisinas/genética; Enuresis Nocturna/etiología; Enuresis Nocturna/genética; Linaje

Palabras clave

Arginine vasopressin; Familial neurohypophyseal diabetes insipidus; Neurophysin II; Polydipsia

Texto completo

Imprimir

XML

PubMed Links

Search on Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Diabetes Insípida Neurogénica / Diabetes Mellitus / Enuresis Nocturna Tipo de estudio: Diagnostic_studies / Etiology_studies Límite: Adult / Child / Female / Humans / Male Idioma: En Año: 2022 Tipo del documento: Article

Texto completo

Imprimir

XML

PubMed Links

Search on Google