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Melkersson-Rosenthal syndrome

Orpha number ORPHA2483
Prevalence of rare diseases Unknown
Inheritance -
Age of onset Childhood
ICD 10 code
  • G51.2
MIM number
Synonym(s) -

Summary

The Melkersson-Rosenthal syndrome is a rare disorder characterized by a triad of recurrent orofacial swelling, relapsing facial paralysis and fissured tongue and onset in childhood or early adolescence. It has an estimated incidence of 8/10,000. The etiology is unknown but hereditary predisposition is suspected. *Author: Orphanet (June 2006)*.

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