| Literature DB >> 19816973 |
N Cindik1, F Ozcay, D Süren, I Akkoyun, M Gökdemir, B Varan, F Alehan, N Ozbek, K Tokel.
Abstract
A 14-year-old female with Gaucher disease presented with hydrocephalus, corneal opacities, cirrhosis, and cardiac valvular involvement. A homozygous D409H mutation was identified. She underwent surgery for aortic and mitral valve replacement. Because of severe calcification of the aortic root, no successful valve replacement was performed. She died on the third day after the explorative cardiac surgery. Cardiac abnormalities represent a life-threatening presentation of the homozygous D409H mutation. Identification of this type is essential prior to initiating appropriate therapy with enzyme replacement and cardiac corrective surgery. Copyright 2010 Wiley Periodicals, Inc.Entities:
Mesh:
Year: 2010 PMID: 19816973 PMCID: PMC6653081 DOI: 10.1002/clc.20348
Source DB: PubMed Journal: Clin Cardiol ISSN: 0160-9289 Impact factor: 2.882