| Literature DB >> 22374380 |
Laura I Rudaks1, Chad Andersen, T Y Khong, Andrew Kelly, Michael Fietz, Christopher P Barnett.
Abstract
Hypertrophic cardiomyopathy (HCM) is a rare presenting feature of congenital disorder of glycosylation type Ia (CDG-Ia). We report two female siblings with CDG-Ia and cardiomyopathy. Patient no. 1 died at 12 days of age from cardiac rupture and tamponade, which has not previously been reported in CDG-Ia. The second patient died at 2 months of age from HCM. The severe cardiac manifestations seen in our patients emphasize the importance of early cardiac assessment in all patients with CDG-Ia.Entities:
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Year: 2012 PMID: 22374380 DOI: 10.1007/s00246-012-0214-y
Source DB: PubMed Journal: Pediatr Cardiol ISSN: 0172-0643 Impact factor: 1.655