Andersen disease

gly·co·ge·no·sis type 4

(glī'kō-jĕ-nō'sis tīp)
Familial cirrhosis with storage of abnormal glycogen; glycogenosis due to deficiency of 1,4-α-glucan branching enzyme, resulting in accumulation of abnormal glycogen with long inner and outer chains in liver, kidney, muscle, and other tissues.
Synonym(s): Andersen disease.
Medical Dictionary for the Health Professions and Nursing © Farlex 2012

Andersen disease

(an?der-sen)
[Dorothy H. Andersen, U.S. pediatrician, 1901–1963]
Glycogen storage disease, type IV.
See: glycogen storage disease
Medical Dictionary, © 2009 Farlex and Partners

Andersen,

Dorothy Hansine, U.S. pediatrician, 1901-1963.
Andersen disease - familial cirrhosis of the liver with storage of abnormal glycogen. Synonym(s): type 4 glycogenosis
Andersen syndrome - cystic fibrosis of the pancreas, vitamin A deficiency, and disease of the abdominal cavity. Synonym(s): Andersen triad
Andersen triad - Synonym(s): Andersen syndrome
Medical Eponyms © Farlex 2012
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.