CINCA syndrome

Get in touch with RARE Concierge.

Contact RARE Concierge

CINCA syndrome

Synonyms: Chronic infantile neurological cutaneous and articular syndrome | IOMID syndrome | Infantile-onset multisystem inflammatory disease | NOMID syndrome | Neonatal-onset multisystem inflammatory disease | Prieur-Griscelli syndrome

A rare genetic cryopyrin-associated periodic syndrome (CAPS) characterized by neonatal onset of systemic inflammation urticarial skin rash and arthritis/arthralgia resulting in severe arthropathy and central nervous system involvement (including chronic aseptic meningitis brain atrophy and sensorineural hearing loss).

Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.

Reference: Access aggregated data from Orphanet at Orphadata.

Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version April 2024

Newly diagnosed with
CINCA syndrome?

Our RARE Concierge Services Guides are available to assist you by providing information, resources and connections as you navigate your rare disease journey.

Get Concierge Help

Advocacy Organizations

Clinical Trials

For a list of clinical trials in this disease area, please click here.