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Griscelli Syndrome Type 2; A Pediatric Case with Immunodeficiency
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نویسنده
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TABATABAIE PARVIZ ,MAHJOUB FATEMEH ,CHERAGHI TAHER ,PARVANEH NIMA
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منبع
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iranian journal of allergy, asthma and immunology - 2007 - دوره : 6 - شماره : 3 - صفحه:155 -157
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چکیده
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A 3,5 month-old girl was admitted with silvery gray hair, light colored skin, recurrentdiarrhea, chest infections, hepatosplenomegaly, episodes of pancyropel1ia, andhemophagocytosis in the bone marrow. light microscopy of hair showcd charnctcrisrir largeand irregular clumps of melanin in the middle of hair shaft. peripheral blood smearexamination did not show giant granules in granulocytes. on the basis of these clinical andlaboratory findings, griscelli syndrome was diagnosed, the child succumbed to infectionduring an accelerated phase of the disease
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کلیدواژه
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Griscclli Syndrome; Immunodeficiency; Phagocyte Disorders
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آدرس
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university of tehran, SCHOOL OF MEDICINE, DEPARTMNET OF PEDIATRIC INFECTIOUS DISEASE, ایران, university of tehran, SCHOOL OF MEDICINE, DEPARTMNET OF PATHOLOGY, ایران, university of tehran, SCHOOL OF MEDICINE, DEPARTMNET OF ALLERGY AND CHINICAL IMMUNOLOGY, ایران, university of tehran, SCHOOL OF MEDICINE, DEPARTMNET OF PEDIATRICS, ایران
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پست الکترونیکی
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dr.parviztabatabaee@yahoo.com
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Authors
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