A recently recognised chronic inflammatory disease of early onset characterised by the triad of rash, central nervous system involvement and arthropathy

Clinical and Experimental Rheumatology

Volumn 19, Issue 1, 2001, Pages 103-106

  Prieur, A M ^a  

^a UNIVERSITÉ PARIS DESCARTES   (France)

Author keywords

Chronic meningitis; Neonatal onset; Systemic disease

Indexed keywords

ANTIRHEUMATIC AGENT; CYTOTOXIC AGENT; GLUCOCORTICOID; NONSTEROID ANTIINFLAMMATORY AGENT;

AMYLOIDOSIS; ARTHROPATHY; ARTICLE; BIRTH; CENTRAL NERVOUS SYSTEM; CHRONIC INFLAMMATION; CINCA SYNDROME; CLINICAL FEATURE; CLINICAL OBSERVATION; DEATH; DISEASE COURSE; FAMILIAL DISEASE; FEVER; HEARING IMPAIRMENT; HUMAN; INFECTION; LIFESPAN; MENINGITIS; PAIN; PRIORITY JOURNAL; PROGNOSIS; RASH; TREATMENT FAILURE; VASCULITIS; VISUAL IMPAIRMENT;

AGE OF ONSET; ARTHRITIS, JUVENILE RHEUMATOID; ARTHROPATHY, NEUROGENIC; CENTRAL NERVOUS SYSTEM DISEASES; CHRONIC DISEASE; EXANTHEMA; HUMANS; INFANT; INFANT WELFARE; INFANT, NEWBORN; INFLAMMATION; SEX FACTORS; SYNDROME;

EID: 0035098521     PISSN: 0392856X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (33)

1. Aspect nosologique des formes systémiques d'arthrite chronique juvénile à début très précoce. A propos de 17 observations
2. Arthropathy with rash, chronic meningitis, neurological changes and arthritis
3. Adult toxoplasmosis in one family
4. Syndrome for diagnosis: Dwarfinism, persistently open fontanel, recurrent meningitis, recurrent subdural effusions with temporary alternate sided hemiplegia; high tone deafness; visual defect with pseudopapilloedena; intellectual development; recurrent acute polyarthritis; erythema marginatum, splenomegaly and iron resistant hypochromic anemia
5. Infantile chronic relapsing inflammation of the brain, skin and joints
6. Familial arthropathy with rash, uveitis and mental retardation
7. Familial vasculitis (life-long morbiliform urticaria, neurological changes and arthritis)
8. Chronic meningitis, polyarthritis, Iymphadenitis and pulmonary hemosiderosis
9. Neonatal onset multisystem inflammatory disease
10. Infantile multisystem inflammatory disease: A specific syndrome?
11. Infantile multisystem inflammatory disease: Another case of a new syndrome
12. Infantile-onset multisystem inflammatory disease
13. Severe refractory neonatal inflammatory syndrome as the manifestation of a systemic multivisceral and meningeal syndrome
14. NOMID - A neonatal syndrome of multisystem inflammation
15. Neonatal onset multisystem inflammatory disease
16. CINCA/NOMID (CN): Further clinical observations
17. Infantile-onset multisystem inflammatory disease: A differential diagnosis of systemic juvenile rheumatoid arthritis
18. Chronic, infantile, neurological, cutaneous and articular syndrome (CINCA) in infant
19. Bi-symptomatic CINCA syndrome with inaugural urticaria and major articular lesions
20. A chronic, infantile, neurological, cutaneous and articular (CINCA) syndrome: A specific entity analysed in 30 patients
21. The chronic, infantile, neurological, cutaneous and articular syndrome (CINCA)
22. The chronic, infantile, neurological, cutaneous and articular syndrome (CINCA Europe, NOMID USA)
23. Ocular manifestations in a recent recognized chronic inflammatory disease of childhood
24. Infantile-onset multisystem inflammatory disease: Radiological findings
25. Joint diseases in the first year of life
26. Mutations in MKV, encoding mevalonate kinase, cause hyeprimmunoglobulinaemia D and periodic fever syndrome
27. Mutations in the gene encoding mevalonate kinase cause hyper-IgD and periodic fever syndrome
28. Early onset "sarcoidosis" and "familial granulomatous arthritis (arteritis)": The same disease
29. Familial granulomatous arthritis, iritis and rash
30. Genetic linkage of familial granulomatous inflammatory arthritis, skin rash, and uveitis to chromosome 16
31. Germline mutations in the extracellular domains of the 55 kDa TNF receptor, TNFR1, define a family of dominantly inherited autoinflammatory syndromes
32. Genetic linkage of the Muckle-Wells syndrome to chromosome 1 q44
33. In vivo study of growth cartilage in children with the infantile onset neurologic, cutaneous and articular syndrome. Inhibitory effect of patient's sera on cultured normal human chondrocyte metabolism