A Case of Microvillous Inclusion Body Disease with Secondary Coagulation Disorder as the First Symptom and Literature Review-Reference-Cited by-同舟云学术

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A Case of Microvillous Inclusion Body Disease with Secondary Coagulation Disorder as the First Symptom and Literature Review

Published:2022 Issue:09 Volume:12 Page:8396-8402
ISSN:2161-8712
Container-title:Advances in Clinical Medicine
language:
Short-container-title:ACM

Author:

马欣颖

Publisher

Hans Publishers

Subject

General Engineering

Reference21 articles.

1. Two cases of microvillus inclusion disease caused by MYO5B deficiency with prenatal abnormalities

2. Unusual feature of neonatal hypernatremic dehydration due to microvillus inclusion disease: a case report

3. MYO5B Pathogenic Variants Found to Cause Intestinal Symptoms Without Microvillus Inclusion Disease in a Child Who Previously Underwent Liver Transplantation for PFIC-like Cholestasis

4. Congenital Diarrhea and Cholestatic Liver Disease: Phenotypic Spectrum Associated with MYO5B Mutations

5. 陈衍晨, 欧阳学军, 王斌. STX3基因突变致微绒毛包涵体病的基因诊断[J]. 发育医学电子杂志, 2018, 6(1): 30-33.

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