両房室弁形成後の逆流急性増悪のために2弁置換を行った新生児Marfan症候群の1例
Author:
Affiliation:
1. Cardiovascular Surgery, Kagoshima City Hospital
2. Cardiovascular Surgery, Kagoshima University Graduate School of Medical and Dental Sciences
3. Cardiovascular Surgery, Fujimoto General Hospital
Publisher
The Japanese Society for Cardiovascular Surgery
Subject
Psychiatry and Mental health
Link
https://www.jstage.jst.go.jp/article/jjcvs/52/2/52_77/_pdf
Reference14 articles.
1. 1) Morisaki H, Morisaki T. Recent progress in the study of molecular pathogenesis of Marfan syndrome. Tokyo Heart J 2007; 27: 12-21.
2. 2) Hennekam RC. Severe infantile Marfan syndrome versus neonatal Marfan syndrome. Am J Med Genet 2005. DOI: 139A, 1. 10.1002/ajmg.a.30979
3. 3) Veiga-Fernández A, Prieto LJ, Álvarez T et al. Perinatal diagnosis and management of early-onset Marfan syndrome: case report and systematic review. J Matern Fetal Neonatal Med 2020; 33: 2493-504.
4. 4) Iwasa T, Ban Y, Doi H et al. Neonatal Marfan syndrome and review of 12 cases in Japan. Ped Cardiol Card Surg 2011; 27: 262-9.
5. 5) Hirano Y, Murakami Y, Sasaki T et al. A case of neonatal Marfan syndrome with medical management(propranolol, losartan etc.) since 1 month of age and mitral valve replacement at 5 years of age. Ped Cardiol Card Surg 2014; 30: 671-5.
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