Keratosis follicularis spinulosa decalvans in Infant/Neonate
KFSD begins in early childhood with keratosis pilaris on the face, which progresses to the trunk and extremities. Limited or widespread cicatricial alopecia of the scalp, eyelashes, and eyebrows ensues. Boys may have corneal dystrophy with associated photophobia. A pustular variant with crusting and scaling on the scalp may occur around puberty. The overall presentation in girls in X-linked dominant cases may be milder than in boys.
For more information on X-linked KFSD, see OMIM.
For more information on autosomal dominant KFSD, see OMIM.
Q82.8 – Other specified congenital malformations of skin
238626006 – Keratosis follicularis spinulosa decalvans
- Keratosis pilaris atrophicans faciei (ulerythema ophryogenes)
- Tinea capitis
- Follicular mucinosis
- Dissecting cellulitis
- Atrichia with papular lesions
- Ichthyosis follicularis alopecia-photophobia syndrome
- Atrophoderma vermiculatum
- Keratitis ichthyosis and deafness syndrome (KID syndrome)
- Lipoid proteinosis
- Graham-Little syndrome
- Lichen planopilaris
- Folliculitis decalvans