Conditions / Skin
primary localized cutaneous amyloidosis 1
info · Skin
A primary cutaneous amyloidosis that has_material_basis_in heterozygous mutation in the gene encoding oncostatin M receptor-beta (OSMR) on chromosome 5p13.
Signs and symptoms
- Lichenification
- Cutaneous amyloidosis
- Pruritus
- Dry skin
- Scaling skin
Also known as: familial primary localized cutaneous amyloidosis-1