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Table 1 (abstract P070). See text for description

From: Proceedings of the 25th European Paediatric Rheumatology Congress (PReS 2018)

 

FMF + Definite JSPA

FMF + Probable JSPA

FMF patients without JIA and JSpA

FMF + JIA (except ERA or JSpA)

Patients, n

32

5

268

15

Female, n (%)

10 (31.25%)

1 (20%)

148 (55.22%)

10 (66.66%)

Age of disease onset, mean ±SD  years

7.19 ± 3.68

5.60 ± 4.93

4.91 ± 3.40

4.93 ± 3.32

Age at study, mean ±SD years

14.84 ± 3.70

13.40 ± 1.67

12.51 ± 4.43

10.73 ± 3.57

M694V mutation n(%)

19 / 30 (63.33%)

3 (60%)

148 / 245 (60.40%)

11 (73.33%)

Disease onset >6 yrs

26 (81.25%)

5 (100%)

 

6 (40%)

Oligorthritis

21 (65.62%)

1 (20%)

14 (93.33%)

Inflammatory back pain

17 / 32 (53.1%)

3 / 5(60%)

0 (0%)

Enthesopathy

 

3 / 5(60%)

0 (0%)

Sacroiliitis

22 /32(68.7%)

0 / 1 (0%)

0 /5 (0%)

Coxofemoral Arthritis

14 /21(66.7%)

19/32(59.37%)

2 / 5(40%)

0 / 15 (0%)

Tarsometatarsal sensivity

 

1 / 5(20%)

1 / 7(14.3%)

HLA-B 27 Positivity

12 / 32 (37.5%)

0 / 1(0%)

0 / 3(0%)

Male Gender

 

4 / 5(80%)

5 /15(33.3%)

Response to NSAID

9 / 22(40.9%)

4 / 5(80%)

2 / 7(28.6%)

Limitation in Schober test (< 4 cm)

22 /32(68.7%)

2 / 5(40%)

0 / 7(0)

21 / 26(80.7%)

Family history of SpA group of disease, dactylitis, psoriasis or presence of IBD

7 / 32(21.87%)

1 / 5(20%)

1 /8(12.5%)

10 / 32(31.3%)