Cryopyrin-associated periodic syndrome (patient information)

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Sahar Memar Montazerin, M.D.[2]

Overview

The cryopyrin-associated periodic syndrome consists of three separate diseases that occur due to a defect in the same gene.

What are the Symptoms of cryopyrin-associated periodic syndrome?

  • The symptoms depend on the severity and type of the disease.
  • Generally, disease severity increases from mild to severe in the following order: familial cold autoinflammatory syndrome (FCAS), Muckle-Wells syndrome, neonatal-onset multisystem inflammatory disease (NOMID).
  • Common symptoms include:
  • FCAS specific symptom is a maculopapular, urticaria-like rash.
  • Symptoms are triggered by cold or cooling temperatures.

What Causes cryopyrin-associated periodic syndrome?

  • CAPS occurs due to a defect in a gene that is responsible for the production of cryopyrin.
  • Cryopyrin is a protein which plays an important role in controlling inflammation.

Who is at Highest Risk?

Diagnosis

When to Seek Urgent Medical Care?

Treatment Options

Where to find Medical Care for cryopyrin-associated periodic syndrome?

  • Medical care for cryopyrin-associated periodic syndrome can be found here.

Prevention

  • There is no preventive method for the cryopyrin-associated periodic syndrome.

What to Expect (Outlook/Prognosis)?

  • Prognosis is poor in the severe form of the disease.

Possible Complications

Sources

http://www.nlm.nih.gov/medlineplus/ency/article/000434.htm

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