Hereditary Hemorrhagic Telangiectasia Patients Detected by Pulmonary Arteriovenous Malformations: Two Pediatric Death Cases from Rupture of Cerebral and Spinal Arteriovenous Malformations
Author:
Affiliation:
1. Department of Cardiology, Kobe Children’s Hospital, Hyogo, Japan
Publisher
The Japanese Society of Pediatric Cardiology and Cardiac Surgery
Subject
Polymers and Plastics,General Environmental Science
Link
https://www.jstage.jst.go.jp/article/jspccs/33/1/33_2016-0035/_pdf
Reference13 articles.
1. 1) White RI Jr, Pollak JS, Wirth JA: Pulmonary arteriovenous malformations: Diagnosis and transcatheter embolotherapy. J Vasc Interv Radiol 1996; 7: 787–804
2. 2) Giordano P, Lenato GM, Suppressa P, et al: Hereditary hemorrhagic telangiectasia: Arteriovenous malformations in children. J Pediatr 2013; 163: 179–186
3. 4) Bossler AD, Richards J, George C, et al: Novel mutations in ENG and ACVRL1 identified in a series of 200 individuals undergoing clinical genetictesting for hereditary hemorrhagic telangiectasia (HHT): Correlation of genotype with phenotype. Hum Mutat 2006; 27: 667–675
4. 5) Al-Saleh S, Mei-Zahav M, Faughnan ME, et al: Screening for pulmonary and cerebral arteriovenous malformations in children with hereditary haemorrhagic telangiectasia. Eur Respir J 2009; 34: 875–881
5. 6) Trerotola SO, Pyeritz RE: PAVM embolization: An update. AJR Am J Roentgenol 2010; 195: 837–845
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