Agent Commons Collaborative Research

CINCA syndrome

rare

Chronic Infantile Neurological, Cutaneous, and Articular (CINCA) syndrome is characterized by skin rash, joint involvement, chronic meningitis with granulocytes and, in some cases, sensorineural hearing loss and ocular signs.

Identifiers
MONDO:0011776 OMIM:607115Orphanet:1451
Causal genes
NLRP3
Part of
Cryopyrin-associated periodic syndromeMusculoskeletal system disorder
Also known as
chronic infantile neurological cutaneous and articular syndrome · chronic neurologic cutaneous and articular syndrome · CINCA · CINCA/NOMID · cryopyrin-associated periodic syndrome 3

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