Uveitis- a rare disease often associated with systemic diseases and infections- a systematic review of 2619 patients

Table 3 Specific entities found in at least 5 patients and age at onset of disease

	Mean	Min	Max	Main (yrs)
JIA	10.8	1	29	<17
APMPPE	20.2	17	27	17-40
Reactive arthritis	34.7	7	66	>17
SLE	30.7	13	53	36-60
Toxoplamosis	29.2	1	79	17-40
Crohn´s disease	34.7	18	64	17-40
Reiter´s disease	35.5	13	64	17-35
Ulcerative colitis	43.4	24	49	17-60
HCF	32.4	12	70	<40
Behcet´s disease	31.1	15	55	<40
Ocular toxocarosis	47.2	11	71	>17
HLA-B27 only eye	37.8	9	82	17-60
Unclassified cases	39.5	2	87	17-60
Psoriatric arthritis	39.8	23	49	36-60
Ancyl. spondylitis	39.5	17	75	17-60
MFC	38.6	16	77	17-60
MS	35.9	14	77	17-40
Sarcoidosis	40.1	5	78	17-60
Serpiginous	45.3	15	76	>36
ARN	43.9	7	62	1 > 17
Ocular herpes	47.8	2	88	>36
Systemic infections	47.5	3	80	17-60
VKH	42.6	30	78	>30
Birdshot	51.4	32	75	36-60
MASQ	55.2	10	80	>36

For each classification, mean age of onset of disease (mean), minimum age at onset of disease (min), maximum age at onset of disease (max) and the main age group where this specific entity is found (main).
JIA: juvenile idiopathic arthritis; APMPPE: acute posterior multifocal placoid pigment epitheliopathy; SLE: systemic lupus erythematosus; HCF: Fuchs’ heterochromic cyclitis; MFC: multifocal choroiditis; MS: multiple sclerosis; ARN: acute retinal necrosis; VKH: Vogt-Koyanagi-Harada disease; MASQ: masquerade syndromes.

ISSN: 1750-1172