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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Hlavní autoři:	Lagen Wan, Hong Wu, Fuyuan Xie, Yijun Nie
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	Taylor & Francis Group 2017-11-01
Edice:	Platelets
Témata:	gaucher cells gba gene mutation thrombocytopenia type 1 gaucher disease
On-line přístup:	http://dx.doi.org/10.1080/09537104.2017.1306044
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