Familial reactive perforating collagenosis
ORPHA:79147· ICD-10 L87.1
Definition
Familial reactive perforating collagenosis is a very rare genetic skin disease characterized by transepidermal elimination of collagen fibers presenting as recurrent spontaneously involuting keratotic papules or nodules.
- Prevalence
- <1 / 1 000 000
- Age of onset
- Childhood