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Barth syndrome is an X-linked disorder characterized by dilated cardiomyopathy, cyclic neutropenia, skeletal myopathy, abnormal mitochondria, and growth deficiency. The primary defect is a mutation in the TAZ gene on the X chromosome at Xq28, resulting in abnormal phospholipid biosynthesis and cardiolipin deficiency. To date, there has been no systematic(More)
OBJECTIVE To present a case of fluconazole-associated torsade de pointes (TDP) and discuss fluconazole's role in causing TDP. CASE SUMMARY A 68-year-old white woman with Candida glabrata isolated from a presacral abscess developed TDP eight days after commencing oral fluconazole The patient had no other risk factors for TDP, including coronary artery(More)
Chronic pleural effusion occurred in three patients, one of whom also developed acute pericarditis. A fourth patient developed both pleural and pericardial effusions. All patients had been receiving dantrolene sodium for at least two months. The pleural fluid was a sterile exudate with pleural and peripheral blood eosinophilia in all patients. No pulmonary(More)
and synthesis (desmosterol), as well as CRP were quantified at baseline and end of study. Results: One hundred and twenty two individuals were included. Atorvas-tatin alone or combined with ezetimibe reduced both LDL-cholesterol and CRP (P<0.002 vs. baseline); ezetimibe did not modify CRP. Reduction in absorption markers was observed in ezetimibe-based(More)
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