Patient - gender

genotype

age at diagnosis (y)

Clinical manifestations

M

 M694V/null

7,6

purpura

F

V726A/null

5,0

purpura, articular involvement, mild gastrointestinal involvement

M

K695R/null

 8,9

purpura, articular involvement, kidney involvement

F

K695R/null

3,1

purpura

F

E148Q/null

2,7

purpura

M

E148Q/null

7,6

purpura, articular involvement

M- male, F- female, y- years
Table 3: Clinical manifestations in individual children with MEFV mutations