Table 1.

Summary table of Neonatal onset multisystem inflammatory disease (NOMID)

ETIOLOGY	NOMID is an autoinflammatory disorder characterized by the triad of neonatal onset of cutaneous symptoms, arthropathy and central nervous system symptoms.
INCIDENCE	Since NOMID is a newly discovered condition and is a very rare condition, the actual incidence and prevalence of the disease is difficult to determine.
GENDER RATIO	Males and females are affected equally
AGE PREDILECTION	Most children are affected before age of 10 years old
RISK FACTORS	It is discovered to be due to alterations in a gene identified as the Cold-induced Auto-inflammatory Syndrome 1 (CIAS1) gene (Autosomal Dominant).
TREATMENT	The treatment is supportive, or aimed solely at controlling symptoms and maximizing function. Some reports showed that early treatment with anakinra related with better outcome of arthropathy.
PROGNOSIS	The prognosis for patients with NOMID is not good and debilitating especially due to the arthropathy.
FINDINGS ON IMAGING	Bulky mass in the physis with heterogenous calcification within.