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

AIM OF THE STUDY: To analyze the clinical features and SLC26A3 mutation of one patient in our hospital who had congenital loss of chlorine diarrhea (CLD), and to investigate the treatment of the disease and the prognosis. MATERIAL AND METHODS: By reviewing the literature, analyzing the clinical feat...

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Detalles Bibliográficos
Autores principales:	Sun, Meiyuan, Tao, Na, Liu, Xiaomei, Yang, Yang, Su, Yanfang, Xu, Fang
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Termedia Publishing House 2021
Materias:	Case report \| Opis przypadku
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10227474/ https://www.ncbi.nlm.nih.gov/pubmed/33599438 http://dx.doi.org/10.5114/pedm.2020.97465

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