A rare case of Bannayan-Riley-Ruvalcaba syndrome with concurrent arteriovenous malformation-Reference-Cited by-同舟云学术

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A rare case of Bannayan-Riley-Ruvalcaba syndrome with concurrent arteriovenous malformation

Published:2024-04 Issue:2 Volume:10 Page:101428
ISSN:2468-4287
Container-title:Journal of Vascular Surgery Cases, Innovations and Techniques
language:en
Short-container-title:Journal of Vascular Surgery Cases, Innovations and Techniques

Author:

Li Rina^ORCID,Skeik Nedaa

Publisher

Elsevier BV

Reference33 articles.

1. Macrocephaly, pseudopapilledema and multiple hemangiomata : a previously undescribed heredofamilial syndrome;Riley;Pediatrics,1960

2. Bannayan-riley-ruvalcaba syndrome in a patient with a pten mutation identified by chromosomal microarray analysis: a case report;Lee;Pediatr Gastroenterol Hepatol Nutr,2017

3. Pten hamartoma tumor syndrome;Yehia,1993

4. Germline ttn variants are enriched in pten-wildtype bannayan–riley–ruvalcaba syndrome;Yehia;npj Genomic Medicine,2017

5. Bannayan-riley-ruvalcaba syndrome with deforming lipomatous hamartomas in infant--case report;Gontijo;An Bras Dermatol,2013

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. Experience of the combined application of sclerotherapy and endovascular embolization in the treatment of venous and arteriovenous malformations of surface location;Ukrainian Interventional Neuroradiology and Surgery;2024-02-14

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