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Case Reports
. 2021 Apr;68(4):e28816.
doi: 10.1002/pbc.28816. Epub 2020 Dec 12.

Double L611S/V617F JAK2 mutation in a child with erythrocytosis

Benjamin Lebecque  1 , Victoria Grèze  2 , Thomas Tassin  1 , Gabrielle Mareynat  1 , Louis-Thomas Dannus  1 , Nathalie Boiret-Dupré  1 , Richard Veyrat-Masson  1 , Nathalie Tribalat  1 , Marc Gabriel Berger  1 , Céline Bourgne  1
Affiliations
Case Reports

Double L611S/V617F JAK2 mutation in a child with erythrocytosis

Benjamin Lebecque et al. Pediatr Blood Cancer. 2021 Apr.
No abstract available

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References

REFERENCES

    1. Cario H. Childhood polycythemias/erythrocytoses: classification, diagnosis, clinical presentation, and treatment. Ann Hematol. 2005;84(3):137-145.
    1. Giona F, Teofili L, Moleti ML, et al. Thrombocythemia and polycythemia in patients younger than 20 years at diagnosis: clinical and biologic features, treatment, and long-term outcome. Blood. 2012;119(10):2219-2227.
    1. Cario H, Schwarz K, Herter JM, et al. Clinical and molecular characterisation of a prospectively collected cohort of children and adolescents with polycythemia vera. Br J Haematol. 2008;142(4):622-626.
    1. Ianotto J-C, Curto-Garcia N, Lauermanova M, Radia D, Kiladjian J-J, Harrison CN. Characteristics and outcomes of patients with essential thrombocythemia or polycythemia vera diagnosed before 20 years of age: a systematic review. Haematologica. 2019;104(8):1580-1588.
    1. Aral B, Courtois M, Ragot S, et al. Germline JAK2 L611S mutation in a child with thrombocytosis. Haematologica. 2018;103(8):e372-e373.

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