Heerfordt syndrome
Synopsis

The precise cause has not been identified. A minority of patients have a close family member with the syndrome. Most patients present as young or middle-aged adults, although the disease may present at any age. There is some evidence to show Heerfordt syndrome may result from a combination of environmental factors and possibly a hereditary component, but the evidence is insufficient.
Prognosis is dependent on managing the patient's underlying systemic symptoms. The disease course is variable as spontaneous remission may occur in over half of patients, while other patients may require more continuous management with corticosteroids.
Codes
D86.89 – Sarcoidosis of other sites
SNOMEDCT:
4416007 – Heerfordt's syndrome
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Last Updated:06/20/2019