Yonsei Med J.  2009 Apr;50(2):307-308.

Primary Pulmonary Hypertension as a Manifestation of Adult Multi-System Mitochondrial Disorder

Affiliations
  • 1Hospital Rudolfstiftung, Vienna, Austria. fifigs1@yahoo.de

Abstract

No abstract available.


MeSH Terms

Aged
Female
Humans
Hypertension, Pulmonary/*etiology
Mitochondrial Diseases/*complications/*pathology/physiopathology

Reference

1. Sproule DM, Dyme J, Coku J, de Vinck D, Rosenzweig E, Chung WK, et al. Pulmonary artery hypertension in a child with MELAS due to a point mutation of the mitochondrial tRNA((Leu)) gene (m.3243A>G). J Inherit Metab Dis. 2008. (in press).
Article
2. Barclay AR, Sholler G, Christodolou J, Shun A, Arbuckle S, Dorney S, et al. Pulmonary hypertension -- a new manifestation of mitochondrial disease. J Inherit Metab Dis. 2005. 28:1081–1089.
Article
3. Van Hove JL, Freehauf C, Miyamoto S, Vladutiu GD, Pancrudo J, Bonilla E, et al. Infantile cardiomyopathy caused by the T14709C mutation in the mitochondrial tRNA glutamic acid gene. Eur J Pediatr. 2008. 167:771–776.
Article
4. Klein A, Fasnacht M, Huisman TA, Neuhaus TJ, Martin E, Boltshauser E. Siblings with infantile cerebral stroke and delayed multivessel involvement -- a new hereditary vasculopathy? Eur J Paediatr Neurol. 2007. 11:292–296.
Article
5. Venditti CP, Harris MC, Huff D, Peterside I, Munson D, Weber HS, et al. Congenital cardiomyopathy and pulmonary hypertension: another fatal variant of cytochrome-c oxidase deficiency. J Inherit Metab Dis. 2004. 27:735–739.
Article
6. Waypa GB, Schumacker PT. Role for mitochondrial reactive oxygen species in hypoxic pulmonary vasoconstriction. Novartis Found Symp. 2006. 272:176–192. discussion 192-5, 214-7.
Article
Full Text Links
  • YMJ
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr