FP51-TH-03 Hydroxychloroquine induced vacuolar myopathy mimicking acid maltase deficiency

2009 ◽  
Vol 285 ◽  
pp. S139 ◽  
Author(s):  
J.H. Tho ◽  
P. Blumbergs
Author(s):  
Angela Genge ◽  
Natasha Campbell

AbstractBackground: Previous reports suggest that although a diagnostic muscle biopsy can confirm the presence of Pompe disease, the absence of a definitive biopsy result does not rule out the diagnosis. Methods: In this study, we reviewed patients with a limb-girdle syndrome who demonstrated nonspecific abnormalities of muscle, without evidence of the classical changes of acid maltase deficiency. These patients were rescreened for Pompe disease using dried blood spot (DBS) testing. Results: Twenty-seven patients provided blood samples for the DBS test. Four patients underwent subsequent genetic testing. Genetic analysis demonstrated that one patient tested positive for Pompe disease and one patient had one copy of a pathogenic variant. Conclusions: In conclusion, the ability of a diagnostic muscle biopsy to definitively rule out the presence of Pompe disease is limited. There is a role for a screening DBS in all patients presenting with a limb-girdle syndrome without a clear diagnosis.


1983 ◽  
Vol 6 (3) ◽  
pp. 201-203 ◽  
Author(s):  
Richard J. Martin ◽  
Robert L. Sufit ◽  
Steven P. Ringel ◽  
David W. Hudgel ◽  
Patricia L. Hill

1985 ◽  
Vol 68 (1) ◽  
pp. 61-74 ◽  
Author(s):  
M. Swash ◽  
M.S. Schwartz ◽  
M.C.P. Apps

Neurology ◽  
2008 ◽  
Vol 70 (8) ◽  
pp. 617-626 ◽  
Author(s):  
A. C. Nascimbeni ◽  
M. Fanin ◽  
E. Tasca ◽  
C. Angelini

2009 ◽  
Vol 96 (2) ◽  
pp. S38
Author(s):  
Charles Roe ◽  
Erland Arning ◽  
Teodoro Bottiglieri ◽  
Arnold Reuser

1990 ◽  
Vol 98 (2-3) ◽  
pp. 169-183 ◽  
Author(s):  
H.A. Kretzschmar ◽  
H. Wagner ◽  
G. Hübner ◽  
A. Danek ◽  
T.N. Witt ◽  
...  

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