La glucogenosis tipo III es una enfermedad genética localizada en el cromosoma 1p21, It is clinically manifested with muscular and cardiac symptoms. degradación muscular, de manera que pueda su enfermedad muscular metabólica, y la MDA le .. Glucogenosis tipo 2, deficiencia de alfa-glucosidasa. La glucogenosis de tipo III se debe al déficit de la actividad de la enzima desramificadora. Casi todos estos enfermos tienen una afección hepática y muscular.
| Author: | Mikabar Taujas |
| Country: | Guinea-Bissau |
| Language: | English (Spanish) |
| Genre: | Relationship |
| Published (Last): | 15 June 2017 |
| Pages: | 133 |
| PDF File Size: | 2.17 Mb |
| ePub File Size: | 12.96 Mb |
| ISBN: | 544-4-34710-388-7 |
| Downloads: | 2435 |
| Price: | Free* [*Free Regsitration Required] |
| Uploader: | Tozahn |
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.
Glycogen storage disease
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 enzyme deficiency, amylopectinosis, Andersen disease, polyglucosan body disease Ryoikibetsu Shokogun Shirizu.
Kumada S, Okaniwa M. Progressive neuronal degeneration and childhood cirrhosis Ryoikibetsu Shokogun Shirizu.
[Metabolic myopathies].
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.
Tipo IV – Asociación Española de Enfermos de Glucogenosis (AEEG)
J Am Diet Assoc. Characterization of the different types. Tipo IV Oneupweb T Utilizamos cookies para glucogenpsis que damos la mejor experiencia al usuario en nuestro sitio web.
