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Children's Health Issues
Hereditary Periodic Fever Syndromes
PFAPA Syndrome
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Topics in Hereditary Periodic Fever Syndromes
  • Overview of Hereditary Periodic Fever Syndromes
  • Familial Mediterranean Fever
  • PFAPA Syndrome
     
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    PFAPA Syndrome

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    PFAPA (periodic fevers with aphthous stomatitis, pharyngitis, and adenitis) syndrome causes recurrent episodes of fever that last 3 to 6 days, mouth sores (stomatitis), a sore throat (pharyngitis), and swollen lymph glands (adenitis). It typically starts between ages 2 and 5 years.

    PFAPA syndrome is a relatively common periodic fever in children. Although a genetic cause has not been established, doctors tend to group PFAPA with hereditary fever syndromes. The syndrome typically starts between the ages of 2 and 5 years and tends to be more common among boys.

    About once a month, children have a fever that lasts 3 to 6 days. The syndrome causes fatigue, chills, and occasionally abdominal pain and headache, as well as fever, sore throat, mouth ulcers, and swollen lymph glands. Children are healthy between episodes, and growth is normal. Children tend to outgrow the syndrome.

    A doctor usually bases the diagnosis on symptoms and the pattern in which they occur. Blood tests may be done to measure substances that indicate inflammation (called markers).

    No treatment is required, but children may be given corticosteroids to relieve symptoms. CimetidineSome Trade Names
    TAGAMET
    seems to cure the syndrome in some children, as may removing the tonsils (tonsillectomy).

    Last full review/revision January 2009 by Stephen E. Goldfinger, MD

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    corticosteroid

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