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propranolol and Glycogen Storage Disease Type II

propranolol has been researched along with Glycogen Storage Disease Type II in 1 studies

Propranolol: A widely used non-cardioselective beta-adrenergic antagonist. Propranolol has been used for MYOCARDIAL INFARCTION; ARRHYTHMIA; ANGINA PECTORIS; HYPERTENSION; HYPERTHYROIDISM; MIGRAINE; PHEOCHROMOCYTOMA; and ANXIETY but adverse effects instigate replacement by newer drugs.
propranolol : A propanolamine that is propan-2-ol substituted by a propan-2-ylamino group at position 1 and a naphthalen-1-yloxy group at position 3.

Glycogen Storage Disease Type II: An autosomal recessively inherited glycogen storage disease caused by GLUCAN 1,4-ALPHA-GLUCOSIDASE deficiency. Large amounts of GLYCOGEN accumulate in the LYSOSOMES of skeletal muscle (MUSCLE, SKELETAL); HEART; LIVER; SPINAL CORD; and BRAIN. Three forms have been described: infantile, childhood, and adult. The infantile form is fatal in infancy and presents with hypotonia and a hypertrophic cardiomyopathy (CARDIOMYOPATHY, HYPERTROPHIC). The childhood form usually presents in the second year of life with proximal weakness and respiratory symptoms. The adult form consists of a slowly progressive proximal myopathy. (From Muscle Nerve 1995;3:S61-9; Menkes, Textbook of Child Neurology, 5th ed, pp73-4)

Research Excerpts

ExcerptRelevanceReference
"Propranolol-treated mice had decreased weight gain (p<0."1.43A beta-blocker, propranolol, decreases the efficacy from enzyme replacement therapy in Pompe disease. ( Han, SO; Kishnani, PS; Koeberl, DD; Li, S; Pope, R; Steet, R, 2016)

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Han, SO1
Pope, R1
Li, S1
Kishnani, PS1
Steet, R1
Koeberl, DD1

Other Studies

1 other study available for propranolol and Glycogen Storage Disease Type II

ArticleYear
A beta-blocker, propranolol, decreases the efficacy from enzyme replacement therapy in Pompe disease.
    Molecular genetics and metabolism, 2016, Volume: 117, Issue:2

    Topics: Adrenergic beta-Antagonists; alpha-Glucosidases; Animals; Cells, Cultured; Drug Antagonism; Drug Eva

2016