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Ghosal Hematodiaphyseal Dysplasia: A Case Report
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نویسنده
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shakiba marjan ,shamsian shahin ,malekzadeh hamid ,yasaei mehrdad
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منبع
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international journal of hematology-oncology and stem cell research - 2020 - دوره : 14 - شماره : 2 - صفحه:127 -129
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چکیده
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Ghosal hematodiaphyseal dysplasia (ghdd) is a rare autosomal recessive disorder presenting with steroid-responsive anemia and diaphyseal dysplasia of long bones. we report a 3-year-old iranian girl with refractory anemia, splenomegaly and radiologic signs of metadiaphyseal dysplasia in long bones. the diagnosis was established by clinical presentation and x-ray bone survey. the patient was treated with oral prednisolone therapy with considerable improvement in anemia and splenomegaly.
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کلیدواژه
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Ghosal syndrome; Anemia; Diaphyseal dysplasia
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آدرس
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shahid beheshti university of medical sciences, mofid children’s hospital, department of pediatric endocrinology and metabolism, Iran, shahid beheshti university of medical sciences, pediatric congenital hematologic disorders research center, mofid children’s hospital, Iran, shahid beheshti university of medical sciences, mofid children’s hospital, department of pediatric endocrinology and metabolism, Iran, shahid beheshti university of medical sciences, mofid children’s hospital, department of pediatric endocrinology and metabolism, Iran
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پست الکترونیکی
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m.yasaei@sbmu.ac.ir
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Authors
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