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- W4387450104 endingPage "1647" @default.
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- W4387450104 abstract "Danon disease is a rare X-linked autophagic vacuolar cardioskeletal myopathy associated with severe heart failure that can be accompanied with extracardiac neurologic, skeletal, and ophthalmologic manifestations. It is caused by loss of function variants in the LAMP2 gene and is among the most severe and penetrant of the genetic cardiomyopathies. Most patients with Danon disease will experience symptomatic heart failure. Male individuals generally present earlier than women and die of either heart failure or arrhythmia or receive a heart transplant by the third decade of life. Herein, the authors review the differential diagnosis of Danon disease, diagnostic criteria, natural history, management recommendations, and recent advances in treatment of this increasingly recognized and extremely morbid cardiomyopathy." @default.
- W4387450104 created "2023-10-10" @default.
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- W4387450104 date "2023-10-01" @default.
- W4387450104 modified "2023-10-13" @default.
- W4387450104 title "International Consensus on Differential Diagnosis and Management of Patients With Danon Disease" @default.
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