/CINCA syndrome

CINCA syndrome

Rare Disease

MONDO:0011776

Also Known As

CINCA syndromeCINCA/NOMIDIOMID syndromeNOMIDNOMID syndromeNeonatal-Onset Multisystem Inflammatory DiseasePrieur-Griscelli syndromechronic infantile neurological cutaneous and articular syndromechronic infantile neurological cutaneous articular syndromechronic neurologic cutaneous and articular syndromecryopyrin-associated periodic syndrome 3infantile-onset multisystem inflammatory diseaseneonatal-onset multisystem inflammatory diseaseCINCACryopyrin-associated periodic syndrome 3IOMIDPrieur Griscelli syndromeinfantile onset multisystem inflammatory diseasemultisystem inflammatory disease, neonatal-onsetneonatal onset multisystem inflammatory disease

Definition

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.

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Associated Genes

NLRP3 ↗

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

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