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diagnosis of gilbert's syndrome in checkup tests: case report
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نویسنده
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rostamipoor mohadeseh ,ashoub muhammad hossein ,obeidi narges
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منبع
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archives of advances in biosciences - 2023 - دوره : 14 - شماره : 1 - صفحه:1 -3
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چکیده
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Introduction: gilbert's syndrome (gs) is an autosomal recessive condition characterized by a relative lack of glucuronyl transferase, inadequate hepatocyte absorption of unconjugated bilirubin, and recurrent bouts of jaundice.case presentation: a 24-year-old male patient was diagnosed with gilbert's syndrome during a routine checkup. all tests except unconjugated bilirubin were normal.conclusion: it was the first report from bushehr. this case was asymptomatic patient which, identified only during routine checkup tests.
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کلیدواژه
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diagnosis ,gilbert's syndrome ,laboratory test
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آدرس
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kerman university of medical sciences, school of para medicine, department of hematology and blood banking, iran, kerman university of medical sciences, school of para medicine, department of hematology and blood banking, iran, bushehr university of medical sciences, school of para medicine, department of hematology, iran
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پست الکترونیکی
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nobeidi@yahoo.com
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Authors
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