scholarly journals Heart Failure Due to Severe Hypertrophic Cardiomyopathy Reversed by Low Calorie, High Protein Dietary Adjustments in a Glycogen Storage Disease Type IIIa Patient

2011 ◽  
pp. 13-16 ◽  
Author(s):  
Christiaan P. Sentner ◽  
Kadir Caliskan ◽  
Wim B. Vletter ◽  
G. Peter A. Smit
Keyword(s):  
Heart Failure ◽  
Hypertrophic Cardiomyopathy ◽  
Glycogen Storage Disease ◽  
Storage Disease ◽  
Glycogen Storage Disease Type ◽  
Glycogen Storage ◽  
Disease Type ◽  
High Protein ◽  
Low Calorie ◽  
Type Iiia

Cognitive impairment in glycogen storage disease type III with severe heart failure: A case report

2021 ◽  
Author(s):  
M. Michaud ◽  
C. Dillier ◽  
M. Selton ◽  
N. Michot ◽  
A. Metzdorf ◽  
...  
Keyword(s):  
Heart Failure ◽  
Cognitive Impairment ◽  
Case Report ◽  
Glycogen Storage Disease ◽  
Storage Disease ◽  
Severe Heart Failure ◽  
Glycogen Storage Disease Type ◽  
Glycogen Storage ◽  
Disease Type ◽  
Type Iii

Heterogeneous mutations in the glycogen-debranching enzyme gene are responsible for glycogen storage disease type IIIa in Japan

2000 ◽  
Vol 106 (1) ◽  
pp. 108-115 ◽  
Author(s):  
M. Okubo ◽  
A. Horinishi ◽  
M. Takeuchi ◽  
Y. Suzuki ◽  
N. Sakura ◽  
...  
Keyword(s):  
Glycogen Storage Disease ◽  
Storage Disease ◽  
Glycogen Storage Disease Type ◽  
Glycogen Storage ◽  
Disease Type ◽  
Debranching Enzyme ◽  
Enzyme Gene ◽  
Type Iiia ◽  
Glycogen Debranching Enzyme

NovelAGLmutation in a Turkish patient with glycogen storage disease type IIIa

2010 ◽  
Vol 52 (1) ◽  
pp. 145-147 ◽  
Author(s):  
Yoshiko Aoyama ◽  
Yoriko Endo ◽  
Tetsu Ebara ◽  
Toshio Murase ◽  
Yoon S. Shin ◽  
...  
Keyword(s):  
Glycogen Storage Disease ◽  
Storage Disease ◽  
Glycogen Storage Disease Type ◽  
Glycogen Storage ◽  
Disease Type ◽  
Turkish Patient ◽  
Type Iiia

scholarly journals Successful Treatment of Severe Cardiomyopathy in Glycogen Storage Disease Type III With D,L-3-Hydroxybutyrate, Ketogenic and High-Protein Diet

2011 ◽  
Vol 70 (6) ◽  
pp. 638-641 ◽  
Author(s):  
Vassili Valayannopoulos ◽  
Fanny Bajolle ◽  
Jean-Baptiste Arnoux ◽  
Sandrine Dubois ◽  
Nathalie Sannier ◽  
...  
Keyword(s):  
Glycogen Storage Disease ◽  
Successful Treatment ◽  
Storage Disease ◽  
High Protein Diet ◽  
Glycogen Storage Disease Type ◽  
Glycogen Storage ◽  
Disease Type ◽  
High Protein ◽  
Protein Diet ◽  
Type Iii

Leucine and glucose kinetics in glycogen storage disease type IIIa

1997 ◽  
Vol 20 (6) ◽  
pp. 847-847 ◽  
Author(s):  
O. A. F. Bodamer ◽  
E. Mayatepek ◽  
J. V. Leonard
Keyword(s):  
Glycogen Storage Disease ◽  
Storage Disease ◽  
Glycogen Storage Disease Type ◽  
Glycogen Storage ◽  
Disease Type ◽  
Glucose Kinetics ◽  
Type Iiia

scholarly journals Data highlighting effects of Ketogenic diet on cardiomyopathy and hepatopathy in Glycogen storage disease Type IIIA

Data in Brief ◽  
2020 ◽  
Vol 32 ◽  
pp. 106205
Author(s):  
Tatiana Marusic ◽  
Mojca Zerjav Tansek ◽  
Andreja Sirca Campa ◽  
Ajda Mezek ◽  
Pavel Berden ◽  
...  
Keyword(s):  
Ketogenic Diet ◽  
Glycogen Storage Disease ◽  
Storage Disease ◽  
Glycogen Storage Disease Type ◽  
Glycogen Storage ◽  
Disease Type ◽  
Type Iiia

scholarly journals Genetic analysis and clinical assessment of four patients with Glycogen Storage Disease Type IIIa in China

2018 ◽  
Vol 19 (1) ◽  
Author(s):  
Yu Zhang ◽  
Mingming Xu ◽  
Xiaoxia Chen ◽  
Aijuan Yan ◽  
Guoyong Zhang ◽  
...  
Keyword(s):  
Genetic Analysis ◽  
Glycogen Storage Disease ◽  
Clinical Assessment ◽  
Storage Disease ◽  
Glycogen Storage Disease Type ◽  
Glycogen Storage ◽  
Disease Type ◽  
Type Iiia

scholarly journals Cardiac Involvement in Glycogen Storage Disease Type IV: Two Cases and the Two Ends of a Spectrum

2012 ◽  
Vol 2012 ◽  
pp. 1-4 ◽  
Author(s):  
Tolga Aksu ◽  
Ayse Colak ◽  
Omac Tufekcioglu
Keyword(s):  
Hypertrophic Cardiomyopathy ◽  
Glycogen Storage Disease ◽  
Storage Disease ◽  
Autosomal Recessive Disorder ◽  
Decompensated Heart Failure ◽  
Glycogen Storage Disease Type ◽  
Glycogen Storage ◽  
Disease Type ◽  
Muscle Disease ◽  
Type Iv

Glycogen storage disease type IV (GSD IV) is an autosomal recessive disorder due to the deficiency ofα1,4-glucan branching enzyme, resulting in an accumulation of amylopectin-like polysaccharide in various systems. We describe two cases, a 23-year-old girl with dilated cardiomyopathy who presented with progressive dyspnea and fatigue and a 28-year-old girl with hypertrophic cardiomyopathy who was asymptomatic, secondary to the accumulation of amylopectin-like fibrillar glycogen, in heart. In both patients, the diagnosis was confirmed by enzyme assessment. Our patients showed that GSD IV is not only liver or skeletal muscle disease, but also it can be presented in different form of the spectrum of cardiomyopathy from dilated to hypertrophic and from asymptomatic to decompensated heart failure. Also, to our knowledge, this is the first hypertrophic cardiomyopathy case due to GSD IV in the literature.

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