amylopectinosis


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amylopectinosis

[‚am·ə·lō‚pek·tə′nō·səs]
(medicine)
A hereditary disease arising from an enzyme deficiency and characterized by abnormal accumulation of glycogen in tissues. Also known as Andersen's disease.
References in periodicals archive ?
Type IV glycogen storage disease (type IV GSD), also known as Andersen disease or amylopectinosis, is a rare autosomal-recessive disorder caused by the deficiency of glycogen branching enzyme.
org 1,2,3,4,7,9 AMSTERDAM DWARF SYNDROME OF DE LANGE See: Cornelia de Lange Syndrome AMYLO-1, 6-GLUCOSIDASE DEFICIENCY See: Glycogen Storage Diseases; Muscular Dystrophy AMYLOPECTINOSIS See: Glycogen Storage Diseases AMYOPLASIA, CONGENITA See: Arthrogryposis Multiplex Congenita ANAL ATRESIA See: Anorectal Malformations ANAL STENOSIS See: Anorectal Malformations ANDERSEN DISEASE See: Glycogen Storage Diseases ANDERSON-FABRY DISEASE See: Fabry Disease ANDERSON-WARBURG SYNDROME See: Norrie Disease ANEMIA, APLASTIC See: Anemia, Fanconi; Bone Marrow Transplant Aplastic Anemia and hyelodysplasia Association of Canada 22 Aikenhead Rd.
org 1,2,3,4,7,9 AMSTERAM DWARF SYNDROME OF DE LANGE See: Cornelia de Lange Syndrome AMYLO-1, 6-GLUCOSIDASE DEFICIENCY See: Glycogen Storage Diseases; Muscular Dystrophy AMYLOPECTINOSIS See: Glycogen Storage Diseases AMYOPLASIA, CONGENITA See: Arthrogryposis Multiplex Congenita ANAL ATRESIA See: Anorectal Malformations ANAL STENOSIS See: Anorectal Malformations ANDERSEN DISEASE See: Glycogen Storage Diseases ANDERSON-FABRY DISEASE See: Fabry Disease ANDERSON-WARBURG SYNDROME See: Norrie Disease ANEMIA, APLASTIC See: Anemia, Fanconi; Bone Marrow Transplant Aplastic Anemia Association of Canada 22 Aikenhead Rd.