type 3 glycogenosis


n.

Glycogenosis due to a deficiency of amylo-1,6-glucosidase, resulting in the accumulation of abnormal glycogen in liver and muscle tissues and characterized by symptoms that are similar to but milder than those of type 1 glycogenosis.Cori's disease debrancher deficiency limit dextrinosis Forbes disease

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The American Heritage® Stedman's Medical Dictionary Copyright © 2002, 2001, 1995 by Houghton Mifflin Company. Published by Houghton Mifflin Company.