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Surgical experience for prolapse of both atrioventricular valves in a patient with filamin A mutation

Published online by Cambridge University Press:  13 February 2014

Takaya Hoashi*
Affiliation:
Department of Pediatric Cardiovascular Surgery, National Cerebral and Cardiovascular Center, Suita, Osaka, Japan
Isao Shiraishi
Affiliation:
Department of Pediatric Cardiology, National Cerebral and Cardiovascular Center, Suita, Osaka, Japan
Hajime Ichikawa
Affiliation:
Department of Pediatric Cardiovascular Surgery, National Cerebral and Cardiovascular Center, Suita, Osaka, Japan
*
Correspondence to: Dr T. Hoashi, MD, PhD, 5-7-1, Fujishiro-dai, Suita, Osaka 565–8565, Japan. Tel: +81 6 6833 5012; Fax: +81 6 6872 7486; E-mail: thoashi@surg1.med.osaka-u.ac.jp

Abstract

A 21-year-old man underwent mitral valve replacement and tricuspid annuloplasty for severe mitral regurgitation and moderate tricuspid regurgitation. Until the operation, he had been treated for hypermobility type Ehlers–Danlos syndrome. Gene examination revealed a mutation in filamin A gene, which is the gene responsible for X-linked myxomatous valvular dystrophy.

Type
Brief Reports
Copyright
© Cambridge University Press 2014 

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References

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