Keratosis follicularis spinulosa decalvans
Medical condition
From Wikipedia, the free encyclopedia
Keratosis follicularis spinulosa decalvans is a rare X-linked disorder described by Siemens in 1926. It is a disease that begins in infancy with keratosis pilaris localized on the face, then evolves to more diffuse involvement.[1]: 580, 762 [2]: 649, 714 [3]
Other namesSiemens-1 syndrome
| Keratosis follicularis spinulosa decalvans | |
|---|---|
| Other names | Siemens-1 syndrome |
| Specialty | Medical genetics |