Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8390452 | Molecular Genetics and Metabolism Reports | 2018 | 4 Pages |
Abstract
There is limited information regarding ideal dosage of alglucoside alfa in patients with Infantile Onset Pompe Disease (IOPD). The U.S. Food and Drug Administration approved alglucoside alfa at dosing of 20â¯mg/kg every other week, but there are small studies and case reports suggesting that dosing higher than this leads to improved ventilator free survival and development without adverse events. We review the clinical course and short term clinical outcomes one year following late diagnosis of IOPD in a 3 month old who presented severely affected and was treated with 40â¯mg/kg twice a week for 21 infusions until six months of age then transitioned to 40â¯mg/kg/week. The patient responded well to 40â¯mg/kg twice a week treatment without adverse reactions and significant clinical improvement.
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Authors
Jesa L. Landis, Holly Hyland, Steven J. Kindel, Ann Punnoose, Gabrielle C. Geddes,