Congenital Tufting Enteropathy, a Rare Cause of Diarrhea and Malnourishment in Arab Child with Genetic and Histopathology Investigations.

IF 0.7 Q4 PEDIATRICS Case Reports in Pediatrics Pub Date : 2023-01-25 eCollection Date: 2023-01-01 DOI:10.1155/2023/6301065
Shooq Alkhalifa, Aysha Darwish, Mohamed Awadh, Salman M Alkhalifa, Abdulla Darwish
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Abstract

Congenital tufting enteropathy (CTE), also known as intestinal epithelial dysplasia (IED), is a rare autosomal recessive disorder due to EPCAM gene mutation. It is a rare congenital enteropathy that presents in early infancy as an intractable diarrhea that is independent of breast formula feeding that requires life-long total parental nutrition (TPN) to acquire adequate calories and fluid intake or small bowel transplantation in severe cases. Here, we report a case of intestinal failure due to congenital tufting enteropathy in a 3-year-old girl who presented with loose stools and failure to thrive. This study aims to review the literature about CTE and discuss the clinicopathological aspects and to be able to distinguish it from other causes of congenital diarrheal disorders (CDDs).

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先天性簇状肠病--阿拉伯儿童腹泻和营养不良的罕见病因及遗传学和组织病理学调查。
先天性簇状肠病(CTE)又称肠上皮发育不良(IED),是一种由于 EPCAM 基因突变引起的罕见常染色体隐性遗传疾病。它是一种罕见的先天性肠病,在婴儿早期表现为难治性腹泻,与母乳配方喂养无关,需要终生全营养(TPN)以获得足够的热量和液体摄入,严重病例还需要进行小肠移植。在此,我们报告了一例因先天性簇状肠病导致肠功能衰竭的病例,患者是一名 3 岁女童,表现为大便稀烂和无法茁壮成长。本研究旨在回顾有关 CTE 的文献,讨论其临床病理方面的问题,并将其与其他原因导致的先天性腹泻病(CDDs)区分开来。
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自引率
11.10%
发文量
48
审稿时长
13 weeks
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