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Pancytopenia: A Rare Presentation of Late Onset Isovaleric Acidemia
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نویسنده
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karami hossein ,zamanfar daniel ,navaifar mohammad reza ,jamallivani parastoo ,rasoli kimia ,naderisorki mohammad
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منبع
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iranian journal of blood and cancer - 2020 - دوره : 12 - شماره : 1 - صفحه:38 -40
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چکیده
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Letter to editor: isovaleric academia was first recognized by tanaka and colleagues as a new genetic disorder of leucine metabolism in two siblings in early infancy. there is a defect in the catabolism of leucine resulting in the accumulation of isovaleric acid.
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آدرس
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mazandaran university of medical sciences, faculty of medicine, thalassemia research center, department of pediatrics hematology and oncology, Iran, mazandaran university of medical sciences, diabetes research center, bou ali sina hospital, department of pediatrics, Iran, mazandaran university of medical sciences, pediatric infectious diseases research center, Iran, mazandaran university of medical sciences, faculty of medicine, student research committe, Iran, mazandaran university of medical sciences, faculty of medicine, student research committe, Iran, mazandaran university of medical sciences, faculty of medicine, student research committe, Iran
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پست الکترونیکی
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dr.naderisorki@gmail.com
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Authors
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