Rarely essential thrombocythemia (ET) is diagnosed in more than one person within a family. Familial myeloproliferative neoplasms are underdiagnosed. In this report, we describe 6 couples of familial ET, evaluating the heterogeneity of the mutational state and the clinical presentation.
Accurso, V., Santoro, M., Mancuso, S., Vajana, G., Tomasello, R., Rotolo, C., et al. (2022). Familial essential thrombocythemia: 6 cases from a mono‐institutional series. CLINICAL CASE REPORTS, 10(3) [10.1002/ccr3.5525].
Familial essential thrombocythemia: 6 cases from a mono‐institutional series
Santoro, MarcoSecondo
Writing – Review & Editing
;Mancuso, Salvatrice;Vajana, Giorgia;Tomasello, Riccardo;Rotolo, Cristina;Camarda, Giulia;Mattana, Marta;Siragusa, Sergio
2022-01-01
Abstract
Rarely essential thrombocythemia (ET) is diagnosed in more than one person within a family. Familial myeloproliferative neoplasms are underdiagnosed. In this report, we describe 6 couples of familial ET, evaluating the heterogeneity of the mutational state and the clinical presentation.
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