|
|
(One intermediate revision by one other user not shown) |
Line 1: |
Line 1: |
| __NOTOC__
| | #redirest [[Cryopyrin-associated periodic syndrome]] |
| {{SI}}
| |
| {{CMG}}
| |
| | |
| {{SK}} NOMID; chronic neurologic cutaneous and articular syndrome; CINCA
| |
| ==Overview==
| |
| '''Neonatal onset multisystem inflammatory disease''' (also known as '''NOMID''', '''Chronic Neurologic Cutaneous and Articular Syndrome''', or '''CINCA''') is a [[rare disease|rare]] genetic [[periodic fever syndrome]] which causes uncontrolled inflammation in multiple parts of the body starting in the newborn period. Symptoms include skin rashes, severe [[arthritis]], and chronic [[meningitis]] leading to neurologic damage.
| |
| | |
| NOMID can result from a mutation in the [[CIAS1]] gene, which helps control inflammation. Mutations in this gene also cause [[familial cold urticaria]] and [[Muckle-Wells syndrome]]. NOMID has been successfully treated with the drug [[anakinra]].
| |
| | |
| ==References==
| |
| *{{OMIM|607115}}
| |
| * Goldbach-Mansky, R. et al. ''Neonatal-Onset Multisystem Inflammatory Disease Responsive to Interleukin-1{beta} Inhibition'' N Engl J Med 2006 355: 581-592.
| |
| | |
| [[Category:Rheumatology]]
| |
| | |
| {{WH}}
| |
| {{WikiDoc Sources}}
| |