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先天性腹泻和婴儿肠病:诊断方法。

Congenital Diarrhea and Enteropathies in Infants: Approach to Diagnosis.

机构信息

Departments of Pediatrics and Pathology, All India Institute of Medical Sciences, New Delhi 110029, India.

出版信息

Indian J Pediatr. 2021 Nov;88(11):1135-1138. doi: 10.1007/s12098-021-03844-z. Epub 2021 Jul 22.

Abstract

Congenital diarrhea and enteropathies (CODEs) are monogenic disorders causing early onset of intractable diarrhea. Their diagnosis and management are challenging. With the availability of commercial next generation genetic testing, we are now better able to classify and manage these disorders. The authors present their experience with 4 cases. Two patients had congenital tufting enteropathy (CTE) and 1 case each of microvillous inclusion disease (MVID) and trichohepatoenteric syndrome (THES). Age at onset varied from 3 to 38 d of life. Light microscopy and electron microscopy of duodenal and rectal endoscopic biopsies were consistent with the diagnosis. Genetic evaluation was possible in 3 cases indicating causative mutations. Two children (CTE and MVID) were alive at last follow-up. The authors suggest a stepwise approach to the diagnosis and management of these disorders in the Indian context.

摘要

先天性腹泻和肠病(CODEs)是一组单基因疾病,可导致早发性难治性腹泻。其诊断和治疗极具挑战性。随着商业下一代基因检测的出现,我们现在能够更好地对这些疾病进行分类和管理。作者介绍了他们的 4 个病例经验。2 例患者患有先天性簇状肠病(CTE),1 例患有微绒毛包涵体病(MVID),1 例患有毛肝肠综合征(THES)。发病年龄从 3 天至 38 天不等。十二指肠和直肠内镜活检的光镜和电镜检查与诊断一致。3 例可进行基因评估,提示存在致病突变。最后一次随访时,有 2 名儿童(CTE 和 MVID)存活。作者建议在印度背景下对这些疾病进行诊断和管理时采用逐步方法。

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