Guerra A S, van Diggelen O P, Carneiro F, Tsou R M, Simoes S, Santos N T
Eur J Pediatr. 1986 Aug;145(3):179-81. doi: 10.1007/BF00446059.
An unusual patient with Andersen disease (glycogenosis type IV) is presented, with only relatively mild clinical symptoms at the age of 8 years. The patient has a profound deficiency of glycogen-branching enzyme.