HubHip: Health: Conditions and Diseases: Neurological Disorders: Brain Diseases: Glycogen Storage Disease Type II (5)

DescriptionAn autosomal recessively inherited glycogen storage disease caused by glucan 1,4-Alpa-Glucosidase Definciency. Large amounts of glycogen accumulate in the lysomes of skeletal muscle ( muscle, skeletal); heart; liver; spinal cord; and brain.

DescriptionAn autosomal recessively inherited glycogen storage disease caused by glucan 1,4-Alpa-Glucosidase Definciency. Large amounts of glycogen accumulate in the lysomes of skeletal muscle ( muscle, skeletal); heart; liver; spinal cord; and brain.

   Glycogen Storage Disease Type II

Last update: 2008-05-06 13:32:07 Glycogen Storage Disease Type II | Copyright 2008 HubHip.com