The case of a boy affected by type III glycogen storage disease and total GH deficiency is reported. Substitutive treatment with hGH caused an extreme elevation of blood lipids. His lipid profile returned near to basal values 1 month after treatment was discontinued. The association of growth hormon
โฆ LIBER โฆ
Severe hypoglycaemia in a patient with glycogen storage disease type III induced by infectious mononucleosis
โ Scribed by T. Kimura; H. Ikeda; M. Kato; A. Ito; M. Okubo; K. Hayasaka
- Book ID
- 110325394
- Publisher
- Springer
- Year
- 2001
- Tongue
- English
- Weight
- 34 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0141-8955
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Glycogen storage disease type III (GSD-III) is an autosomal recessive disease resulting from deficient glycogen debranching enzyme (ODE) activity. A child with GDE deficient in both liver and muscle (GSD-IIIa) had recurrent hypoglycemia, seizures, severe cardiomegaly, and hepatomegaly and died at 4