Glycogen Storage Disease Type II Clinical Trial
Official title:
Effect of Motor Development, Motor Function and Electrodiagnostic Characteristic of IOPD Under ERT
To investigate the motor development, motor function and electrodiagnostics presentation in IOPD under ERT.
Background
Pompe disease is an autosomal recessive disease, enzyme replacement therapy (ERT) and new
born screen (NBS) had been initiated in Taiwan since 2008. However, residual muscle weakness
were noted. Decrease in amplitude of nerve compound muscle action potential (CMAP) and
increase spontaneous activity were reported before the imitation of ERT. However, the motor
development, motor function and electrodiagnostic presentation which were important in
further direction of treatment and rehabilitation program arrangement in infantile Pompe
disease (IOPD) under ERT is lacking.
Aim
To investigate the motor development, motor function and electrodiagnostic presentation in
IOPD under ERT.
Method
This is an observational, prospective, longitudinal, follow-up study. Motor development was
assessed by Alberta Infant Motor Scale (AIMS) and Peabody Developmental Motor Scales, Second
Edition (PDMS II); motor function was assessed by Pediatric Evaluation of Disability
Inventory (PEDI) and Gross Motor Function Measure (GMFM). Electrodiagnosis studies include
nerve conduction study (NCS) and electromyography (EMG).
Expect Effects
Obtain the characteristics of motor development, motor function and electrodiagnosis
presentation of IOPD under ERT, and the relation between motor development, motor function
and electrodiagnosis presentation.
;
Observational Model: Cohort, Time Perspective: Prospective
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