Thrombocytopenia and GBA gene mutation in a patient with adult type 1 Gaucher disease
A 38-year-old female patient was diagnosed with anemia for 3 years. Medical examination showed slight splenomegaly (250 × 62 mm), thrombocytopenia (platelets 51 × 109/L), anemia (Hb levels 107 g/L), and β-glucocerebrosidase activity (GBA) in leukocytes was lower than normal. Microscopic findings of...
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| Hoofdauteurs: | , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Taylor & Francis Group
2017-11-01
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| Reeks: | Platelets |
| Onderwerpen: | |
| Online toegang: | http://dx.doi.org/10.1080/09537104.2017.1306044 |
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