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, Marco
Secondo
Writing – Review & Editing
;
Mancuso, Salvatrice;Vajana, Giorgia;Tomasello, Riccardo;Rotolo, Cristina;Camarda, Giulia;Mattana, Marta;Siragusa, Sergio
2022

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.
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].
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/10447/537190
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