Hennekam syndrome: an uncommon cause of chylous ascites and intestinal lymphangiectasia in the tropics-Reference-Cited by-同舟云学术

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Hennekam syndrome: an uncommon cause of chylous ascites and intestinal lymphangiectasia in the tropics

Published:2019-07 Issue:7 Volume:12 Page:e229419
ISSN:1757-790X
Container-title:BMJ Case Reports
language:en
Short-container-title:BMJ Case Rep

Author:

Menon Jagadeesh,Venkatesh Vybhav,Thirunavukkarasu Balamurugan,Lal Sadhna Bhasin

Abstract

Paediatric chylous ascites in tropics is commonly caused by infections and trauma. We describe the clinical characteristics of an uncommon inherited cause of chylous ascites, Hennekam syndrome, treated by nutritional modification.

Publisher

BMJ

Subject

General Medicine

Reference7 articles.

1. Autosomal recessive intestinal lymphangiectasia and lymphedema, with facial anomalies and mental retardation

2. Mutations in CCBE1 cause generalized lymph vessel dysplasia in humans

3. Centre for Arab Genomic Studies, A Division of Sheikh Hamdan Award for Medical Sciences. Hennekam Lymphangiectasia–Lymphedema Syndrome. The Catalogue for Transmission Genetics in Arabs, CTGA Database :1–2.

4. Missense mutations interfere with VEGFR-3 signalling in primary lymphoedema

5. Intestinal lymphangiectasia, lymphedema, mental retardation, and typical face: Confirmation of the Hennekam syndrome

Cited by 1 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. Newfound features associated with Hennekam Syndrome (Intestinal Lymphangiectasia–Lymphedema–Intellectual–Disability Syndrome) complicated with comorbid Waldmann's Disease resulting in Celiac Disease;Clinical Case Reports;2023-11

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