Clinical Cardiology · 2009 · 30 citations · 13 references
Life SciencesCardiologyGeneticsCardiovascular GeneticsHuman GeneticsMedical GeneticsCongenital DisordersCongenital Heart DiseaseGenetic Disease PathologyGenetic DisordersGenetic SyndromesLysosomal Storage DisordersAortic Root DiseaseCalcificationCommunicating Hydrocephalus TreatmentCongenital Enzyme DefectsEnzyme Replacement TherapyGaucher DiseaseInherited VariantsValve Abnormalities
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.
13
The metabolic basis of inherited disease
JL Goldstein · Medical Entomology and Zoology · 1995 · 1K citations
Cardiac manifestations of Fabry's disease
Anton E. Becker, Rein Schoorl, A G Balk et al. · The American Journal of Cardiology · 1975 · 103 citations
Medicine, Cardiology, Pathology +11