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- W2067025769 abstract "A 17-month boy with history of neutropenia and gross motor regression was found to have cardiomyopathy upon admission. He was diagnosed with Barth syndrome: dilated cardiomyopathy, neutropenia, skeletal myopathy, decreased stature, and 3-methylglutaconic aciduria, confirmed by tafazzin gene deletion. This diagnosis should be considered in boys with unexplained neutropenia." @default.
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- W2067025769 date "2008-10-01" @default.
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- W2067025769 title "Cardiomyopathy in a child with neutropenia and motor delay" @default.
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- W2067025769 doi "https://doi.org/10.1097/mop.0b013e32830a990a" @default.
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