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Bone marrow fibrosis, sequence variant of asxl1, and Sjögren syndrome: A case report
- Source :
- Clinical Case Reports, Clinical Case Reports, Vol 8, Iss 7, Pp 1269-1273 (2020), Dipòsit Digital de Documents de la UAB, Universitat Autònoma de Barcelona
- Publication Year :
- 2020
- Publisher :
- John Wiley and Sons Inc., 2020.
-
Abstract
- Only proven pathogenic mutations associated with myeloid neoplasms are key to establish the clonal nature of the bone marrow fibrosis. In cases with genetic variants of uncertain meaning, the clinical picture may be required to rule out secondary causes.
- Subjects :
- Myeloid
lcsh:Medicine
Bone marrow fibrosis
Case Report
Case Reports
030204 cardiovascular system & hematology
Sjögren syndrome
ASXL1
03 medical and health sciences
0302 clinical medicine
medicine
molecular
Sequence (medicine)
lcsh:R5-920
business.industry
lcsh:R
Genetic variants
Molecular
autoimmune
General Medicine
medicine.disease
medicine.anatomical_structure
bone marrow fibrosis
030220 oncology & carcinogenesis
Immunology
business
lcsh:Medicine (General)
Autoimmune
Subjects
Details
- Language :
- English
- ISSN :
- 20500904
- Volume :
- 8
- Issue :
- 7
- Database :
- OpenAIRE
- Journal :
- Clinical Case Reports
- Accession number :
- edsair.doi.dedup.....2d5d9bc6ce9b63c6f737be8758436599