Familial Primary Localized Cutaneous Amyloidosis Results from Either Dominant or Recessive Mutations in OSMR.

The article discusses research which investigated occurrence of familial primary localized cutaneous amyloidosis (FPLCA) in two families. Topics explored include pathogenic mutations that are commonly associated with FPLCA, the clinical and histopathological evaluation of the blood samples gathered from participating family members, and the oncostatin M receptor (OSMR) mutations observed in FPLCA patients.