Abstract
Myocarditis attributed to Epstein-Barr virus (EBV) as the sole cause is a rare manifestation. Myocarditis ascribed to EBV infection in combination with other factors has been reported in a few more cases. We report a child who experienced active EBV infection and later, at 19 months of age, received a diagnosis of Pompe disease (acid alpha-glucosidase deficiency) with predominant cardiac involvement. The cardiac symptoms resolved at the end of the EBV infection. When the patient was recently seen, at 8 years of age, she had an increased left ventricular wall thickness but normal cardiac function. DNA analysis identified this patient as compound heterozygote for a mutant Tyr292Cys and a null allele. In light of genotype-phenotype correlation, it is notable that a Spanish patient with a functionally similar genotype (Tyr292Cys/Arg854Stop) also had childhood Pompe disease with peripheral muscular involvement.
Original language | English |
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Article number | 65 |
Number of pages | 2 |
Journal | Pediatrics |
Volume | 109 |
Issue number | 4 |
DOIs | |
Publication status | Published - Apr-2002 |
Keywords
- cardiomyopathy
- Pompe disease
- Epstein-Barr virus
- acid alpha-glucosidase
- MYOCARDITIS
- MUTATION