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Markedly elevated serum biotinidase activity may indicate glycogen storage disease type Ia.

作者信息

Wolf B, Freehauf C L, Thomas J A, Gordon P L, Greene C L, Ward J C

机构信息

Department of Pediatrics, Connecticut Children's Medical Center, 282 Washington Street, Hartford, CT 06106, USA.

出版信息

J Inherit Metab Dis. 2003;26(8):805-9. doi: 10.1023/B:BOLI.0000009949.65855.4c.

Abstract

We report two children who presented with symptoms suggestive of biotinidase deficiency. Rather than deficiency, markedly elevated serum biotinidase activities were found. Based upon literature reports of elevated biotinidase activities in children with glycogen storage disease (GSD) type Ia, we considered the latter in our differential diagnosis and subsequently confirmed GSD type Ia in both patients by enzymatic testing. GSD type Ia should be considered in children with markedly elevated serum biotinidase activity.

摘要

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