Microvillus Inclusion Disease: Prenatal Ultrasound Findings, Molecular Diagnosis and Genetic Counseling of Congenital Diarrhea-Reference-Cited by-同舟云学术

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Microvillus Inclusion Disease: Prenatal Ultrasound Findings, Molecular Diagnosis and Genetic Counseling of Congenital Diarrhea

Published:2010-12 Issue:4 Volume:49 Page:487-494
ISSN:1028-4559
Container-title:Taiwanese Journal of Obstetrics and Gynecology
language:en
Short-container-title:Taiwanese Journal of Obstetrics and Gynecology

Author:

Chen Chih-Ping,Chiang Ming-Chou,Wang Tzu-Hao,Hsueh Chuen,Chang Shueen-Dyh,Tsai Fuu-Jen,Wang Chao-Ning,Chern Schu-Rern,Wang Wayseen

Publisher

Elsevier BV

Subject

Obstetrics and Gynaecology

Reference27 articles.

1. Congenital diarrheal disorders: improved understanding of gene defects is leading to advances in intestinal physiology and clinical management;Berni Canani;J Pediatr Gastroenterol Nutr,2010

2. Familial enteropathy: a syndrome of protracted diarrhea from birth, failure to thrive, and hypoplastic villous atrophy;Davidson;Gastroenterology,1978

3. Familial microvillous atrophy: a clinicopathological survey of 23 cases;Phillips;J Pediatr Gastroenterol Nutr,1992

4. Microvillous inclusion disease (microvillous atrophy);Ruemmele;Orphanet J Rare Dis,2006

5. Ultrastructural aspects of enterocyte defects in infancy and childhood;Iancu;Ultrastruct Pathol,2010

Cited by 21 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A Case of Microvillous Inclusion Body Disease with Secondary Coagulation Disorder as the First Symptom and Literature Review;Advances in Clinical Medicine;2022

2. Microvillus Inclusion Disease and Tufting Enteropathy;Textbook of Pediatric Gastroenterology, Hepatology and Nutrition;2021-11-25

3. Monogenic mutations in four cases of neonatal-onset watery diarrhea and a mutation review in East Asia;Orphanet Journal of Rare Diseases;2021-09-09

4. Antenatal diagnosis of microvillus inclusion disease;Obstetrics & Gynecology International Journal;2021-08-12

5. Congenital Diarrhea and Cholestatic Liver Disease: Phenotypic Spectrum Associated with MYO5B Mutations;Journal of Clinical Medicine;2021-01-28

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