Literature DB >> 27106438

Palliative Mitral Valve Repair During Infancy for Neonatal Marfan Syndrome.

Hiroto Kitahara1, Ryo Aeba2, Hidenobu Takaki1, Hideyuki Shimizu1.   

Abstract

An infant with neonatal Marfan syndrome (nMFS), a condition that is nearly always lethal during infancy, was referred to our hospital with symptoms of congestive heart failure resulting from severe mitral valve insufficiency. During mitral valve repair, the use of an annuloplasty ring was waived until annular dilatation was achieved after 2 palliative mitral valvuloplasty procedures. After the definitive operation, the patient's mitral valve function remained within normal limits until the last follow-up when the patient was 11 years old. To the best of our knowledge, this patient has the longest recorded survival after mitral valve repair.
Copyright © 2016 The Society of Thoracic Surgeons. Published by Elsevier Inc. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2016        PMID: 27106438     DOI: 10.1016/j.athoracsur.2015.06.115

Source DB:  PubMed          Journal:  Ann Thorac Surg        ISSN: 0003-4975            Impact factor:   4.330


  1 in total

1.  Nonmyocyte ERK1/2 signaling contributes to load-induced cardiomyopathy in Marfan mice.

Authors:  Rosanne Rouf; Elena Gallo MacFarlane; Eiki Takimoto; Rahul Chaudhary; Varun Nagpal; Peter P Rainer; Jay G Bindman; Elizabeth E Gerber; Djahida Bedja; Christopher Schiefer; Karen L Miller; Guangshuo Zhu; Loretha Myers; Nuria Amat-Alarcon; Dong I Lee; Norimichi Koitabashi; Daniel P Judge; David A Kass; Harry C Dietz
Journal:  JCI Insight       Date:  2017-08-03
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.