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- W2001851208 abstract "Homocystinuria is an inborn error of amino acid metabolism in which homocystine accumulates in the blood and produces a slowly evolving clinical syndrome. We are presenting a case of a 4-year-old female child who presented to us with stroke and also had megaloblastic anemia. She was diagnosed as having homocystinuria type-1, and she responded to treatment." @default.
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- W2001851208 date "2010-01-01" @default.
- W2001851208 modified "2023-10-14" @default.
- W2001851208 title "Homocystinuria: A rare condition presenting as stroke and megaloblastic anemia" @default.
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- W2001851208 doi "https://doi.org/10.4103/1817-1745.76110" @default.
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