Familial cold autoinflammatory syndrome 3

Common Name(s)

Familial cold autoinflammatory syndrome 3

Familial cold autoinflammatory syndrome-2 is an autosomal dominant immune disorder characterized by the development of cutaneous urticaria, erythema, and pruritus in response to cold exposure. Affected individuals have variable additional immunologic defects, including antibody deficiency, decreased numbers of B cells, defective B cells, increased susceptibility to infection, and increased risk of autoimmune disorders (summary by {2:Ombrello et al., 2012}). For a discussion of genetic heterogeneity of FCAS, see FCAS1 ({120100}).
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Familial cold autoinflammatory syndrome 3" for support, advocacy or research.

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Scientific Literature

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Clinical Trial Information This information is provided by ClinicalTrials.gov

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