Glycogen Storage disease

I (glucose-6-phosphatase deficiency, Von Gierke)
II (alpha glucosidase deficiency, Pompe)
III (debrancher enzyme deficiency, Cori)
IV (brancher enzyme deficiency, Anderson)
V (muscle glycogen phosphorylase deficiency, McArdle)

VII (muscle phosphofructokinase deficiency, Tauri)
VI (liver phosphorylase deficiency, Hers)

IX (liver glycogen phosphorylase kinase deficiency)

Association for Glycogen Storage (AGSD): PO Box 896; Durant, IA 52747-9769; Phone: 563.785.6038 (also fax); Web site: www.agsdus.org
Association for Glycogen Storage Disease (UK)

Pompe Disease Page, United Kingdom

Association Francophone des Glycogenoses (French Glycogen Storage Disease Association): Rue G. Guynemer
37390 La Membrolle S/Choiselle
Tel et Fax: 02.47.87.03.18; E-mail: ahugon@infonie.fr

Acid Maltase Deficiency Association (GSD type II): P.O. Box 700248
San Antonio, Texas 78270-0248
Phone: 210-494-6144 or 210-490-7161
Fax: 210-490-7161 or 210-497-3810; E-mail: tianrama@aol.com

Also See:

National organizations, information on genetic conditions or birth defects
American Liver Foundation, Type I Glycogan Storage Disease Pamphlet
McArdles Page, Type V information, family page by RSpeary, UK

locate a genetic counselor or clinical geneticist:

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