Bone marrow fibrosis, sequence variant of asxl1, and Sjögren syndrome: A case report.
ASXL1
Sjögren syndrome
autoimmune
bone marrow fibrosis
molecular
Journal
Clinical case reports
ISSN: 2050-0904
Titre abrégé: Clin Case Rep
Pays: England
ID NLM: 101620385
Informations de publication
Date de publication:
Jul 2020
Jul 2020
Historique:
received:
25
09
2019
revised:
18
02
2020
accepted:
29
02
2020
entrez:
23
7
2020
pubmed:
23
7
2020
medline:
23
7
2020
Statut:
epublish
Résumé
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.
Identifiants
pubmed: 32695373
doi: 10.1002/ccr3.2813
pii: CCR32813
pmc: PMC7364095
doi:
Types de publication
Case Reports
Langues
eng
Pagination
1269-1273Informations de copyright
© 2020 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd.
Déclaration de conflit d'intérêts
None declared.
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