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Refractory chronic "ITP": When platelet size matters
Uppsala University, Science for Life Laboratory, SciLifeLab. Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Immunology, Genetics and Pathology, Experimental and Clinical Oncology. Uppsala Univ Hosp, Dept Clin Genet, Uppsala, Sweden.ORCID iD: 0000-0002-5634-7156
Orebro Univ Hosp, Dept Med, Sect Hematol, Orebro, Sweden.
Copenhagen Univ Hosp, Ctr Genom Med, Copenhagen, Denmark.
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Immunology, Genetics and Pathology, Clinical and experimental pathology. (Rose-Marie Amini)
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
2018. Vol. 6, no 9, p. 1779-1780
Keywords [en]
ear nose and throat, genetics, hematology, nephrology, pediatrics and adolescent medicine
National Category
Hematology Clinical Laboratory Medicine
Research subject
Pathology
Identifiers
URN: urn:nbn:se:uu:diva-365664DOI: 10.1002/ccr3.1711ISI: 000444225900027PubMedID: 30214762OAI: oai:DiVA.org:uu-365664DiVA, id: diva2:1263317
Available from: 2018-11-15 Created: 2018-11-15 Last updated: 2019-03-29Bibliographically approved

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