Wiskott-Aldrich syndrome with unusual clinical features similar to juvenile myelomonocytic leukemia
Wiskott-Aldrich syndrome with unusual clinical features similar to juvenile myelomonocytic leukemia
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Publisher
Japan: Springer Japan
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Language
English
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Publisher
Japan: Springer Japan
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Contents
A male infant exhibited thrombocytopenia at birth, and later developed leukocytosis, monocytosis, and bloody stool. The bone marrow was hypercellular with dysplasia. Spontaneous granulocyte/macrophage-colony formation and hypersensitivity to granulocyte/macrophage-colony stimulating factor were confirmed by in vitro culture. These findings fulfille...
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Full title
Wiskott-Aldrich syndrome with unusual clinical features similar to juvenile myelomonocytic leukemia
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TN_cdi_proquest_miscellaneous_1034656824
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_1034656824
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ISSN
0925-5710
E-ISSN
1865-3774
DOI
10.1007/s12185-012-1130-x