Familial multiple discoid fibromas
ORPHA:538756· ICD-10 D23.9
Definition
A rare, genetic, skin tumor disorder characterized by childhood-onset of multiple, benign, asymptomatic, white to flesh-colored papules predominantly located on the face, ears, neck and trunk, not associated with systemic organ involvement, malignancies or FLCN gene locus mutation.
- Prevalence
- <1 / 1 000 000
- Age of onset
- Adolescent, Adult, Childhood, Infancy, Neonatal