Table 1

Incidence of myeloproliferative markers and hereditary polycythemia markers in 13 children with PV

MarkerSporadic polycythemiaFamilial polycythemia
No. 
JAK2V617F mutation, no. patients (%) 3 (37) 
Exon 12 JAK2 mutations, no. patients (%) 
Epo-R mutations, no. patients (%) 
Low serum Epo, no. patients (%) 2 (25) 
EEC growth, no. patients (%) 3 (37) 1 (20) 
Clonal hematopoiesis, no. patients* 2/2 0/3 
PV diagnosis, no. patients (%) 5 (62) 1 (20) 
    2 major + 1 minor, no. patients (%) 3 (37) 
    1 major + 2 minor, no. patients (%) 2 (25) 1 (20) 
MarkerSporadic polycythemiaFamilial polycythemia
No. 
JAK2V617F mutation, no. patients (%) 3 (37) 
Exon 12 JAK2 mutations, no. patients (%) 
Epo-R mutations, no. patients (%) 
Low serum Epo, no. patients (%) 2 (25) 
EEC growth, no. patients (%) 3 (37) 1 (20) 
Clonal hematopoiesis, no. patients* 2/2 0/3 
PV diagnosis, no. patients (%) 5 (62) 1 (20) 
    2 major + 1 minor, no. patients (%) 3 (37) 
    1 major + 2 minor, no. patients (%) 2 (25) 1 (20) 

The number of patients fulfilling the proposed revised WHO diagnostic criteria for PV is shown in the lower part of the table.

*

Number of patients with clonal hematopoiesis among all female patients.

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