Avatrombopag improves thrombocytopenia in MYH9-related disorder following eltrombopag treatment failure
MYH9-related disorder (MYH9-RD) is autosomal dominant thrombocytopenia caused by mutations in the MYH9 gene, which codes for the non-muscle myosin-IIA heavy chain. We present a case of a 24-year-old Chinese man with MYH9-RD who was initially misdiagnosed with immune thrombocytopenia. Whole-exome seq...
محفوظ في:
| المؤلفون الرئيسيون: | , , , , , |
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| التنسيق: | Artigo |
| اللغة: | Inglês |
| منشور في: |
Taylor & Francis Group
2022-11-01
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| سلاسل: | Platelets |
| الموضوعات: | |
| الوصول للمادة أونلاين: | http://dx.doi.org/10.1080/09537104.2022.2096211 |
| الوسوم: |
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