Congenital chloride diarrhea in patient with SLC26A2 mutation - analysis of the clinical phenotype and differential diagnosis.

Sun, Meiyuan; Tao, Na; Liu, Xiaomei; Yang, Yang; Su, Yanfang; Xu, Fang

Sun, Meiyuan; Tao, Na; Liu, Xiaomei; Yang, Yang; Su, Yanfang; Xu, Fang.

Afiliación

Sun M; Endocrinology, Kunming Children's Hospital, China.
Tao N; Yunnan Key Laboratory of Children's Major Disease Research, China.
Liu X; Endocrinology, Kunming Children's Hospital, China.
Yang Y; Yunnan Key Laboratory of Children's Major Disease Research, China.
Su Y; Endocrinology, Kunming Children's Hospital, China.
Xu F; Yunnan Key Laboratory of Children's Major Disease Research, China.

Pediatr Endocrinol Diabetes Metab ; 2020 Nov 16.

Article en En | MEDLINE | ID: mdl-33191723

Palabras clave

SLC26A3 gene; electrolyte acid-base imbalance differential diagnosis.; congenital chloride diarrhea

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Diagnostic_studies / Prognostic_studies Idioma: En Revista: Pediatr Endocrinol Diabetes Metab Asunto de la revista: ENDOCRINOLOGIA / METABOLISMO / PEDIATRIA Año: 2020 Tipo del documento: Article País de afiliación: China Pais de publicación: Polonia

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