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Refractory chronic "ITP": When platelet size matters
Department of Clinical Genetics, Uppsala University Hospital, Uppsala, Sweden; Science for Life Laboratory, Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
Örebro University, School of Medical Sciences. Section of Hematology.
Center for Genomic Medicine, Copenhagen University Hospital, Copenhagen, Denmark.
Department of Immunology, Genetics and Pathology, Clinical and Experimental Pathology, Uppsala University and Uppsala University Hospital, Uppsala, Sweden.
2018 (English)In: Clinical Case Reports, E-ISSN 2050-0904, Vol. 6, no 9, p. 1779-1780Article in journal (Refereed) Published
Abstract [en]

Key Clinical Message

Inherited conditions associated with thrombocytopenia should be included in the differential diagnosis of young patients with refractory immune thrombocytopenia (ITP), even in the absence of a positive family history. Early identification of such conditions is of vital importance in order to reach the right diagnosis and avoid unnecessary or even harmful medication.

Place, publisher, year, edition, pages
John Wiley & Sons, 2018. Vol. 6, no 9, p. 1779-1780
Keywords [en]
ear nose and throat, genetics, hematology, nephrology, pediatrics and adolescent medicine
National Category
General Practice
Identifiers
URN: urn:nbn:se:oru:diva-69096DOI: 10.1002/ccr3.1711ISI: 000444225900027PubMedID: 30214762Scopus ID: 2-s2.0-85050616404OAI: oai:DiVA.org:oru-69096DiVA, id: diva2:1252266
Available from: 2018-10-01 Created: 2018-10-01 Last updated: 2018-10-01Bibliographically approved

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Kättström, Magdalena

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