The clinical manifestations of glycogen storage disease type IV (GSD IV) discussed in this entry span a continuum of different subtypes with. GSD IV GLYCOGEN BRANCHING ENZYME DEFICIENCY GBE1 DEFICIENCY ANDERSEN DISEASE BRANCHER DEFICIENCY GLYCOGENOSIS IV. Spanish Synonyms of “enfermedad por almacenamiento de gluc√≥geno-tipo IV”: EAG tipo IV, enfermedad de Andersen, glucogenosis tipo IV.

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Congenital form of glycogen storage disease type IV: The intracellular transport of chylomicrons requires the small GTPase, Sar1b.


The genes and proteins of atherogenic lipoprotein production. Rev Endocr Metab Disord.

An expanding view for the molecular basis of familial periodic paralysis. Myophosphorylase deficiency glycogenosis type V; McArdle disease.

Moses SW, Parvari R. The variable presentations of glycogen storage disease type IV: Glycogen branching enzyme deficiency Andersen disease Ryoikibetsu Shokogun Shirizu. Glycogenosis type IV branching glucognosis deficiency, amylopectinosis, Andersen disease, polyglucosan body disease Ryoikibetsu Shokogun Shirizu.

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Kumada S, Okaniwa M. Progressive neuronal degeneration and childhood cirrhosis Ryoikibetsu Shokogun Shirizu. Severe cardiomyopathy revealing amylopectinosis.

Two cases in adolescents from the same family Presse Med. Goldberg T, Slonim AE.

Nutrition therapy for hepatic glycogen storage diseases. J Am Diet Assoc. Characterization of the different types. Tipo IV Oneupweb T Utilizamos cookies para asegurar que damos la mejor experiencia al usuario en nuestro tio web.