Chronic infantile neurological cutaneous and articular syndrome

CINCA syndrome is a rare congenital inflammatory disorder characterized by a triad of neonatal onset of cutaneous symptoms, chronic meningitis, and joint manifestations with recurrent fever and inflammation.

Alternative names

FCAS, CINCA, NOMID

Multisystem inflammatory disease, neonatal-onset

Neonatal onset multisystem inflammatory disease

Chronic infantile neurologic cutaneous articular syndrome

Classification

  • Periodic fever syndromes
    • Cold autoinflammatory syndrome

Inheritance

Autosomal dominant

OMIM

#607115 CINCA syndrome

*606416 Cias1 gene; CIAS1

Incidence

Incidence is not known.