65 top medical experts on X-Linked Keratosis Follicularis Spinulosa Decalvans across 7 countries and 2 U.S. states, including 5 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.
- X-Linked Keratosis Follicularis Spinulosa Decalvans: Keratosis follicularis spinulosa decalvans is a rare genodermatosis occurring during infancy or childhood, predominantly affecting males, and characterized by diffuse follicular hyperkeratosis associated with progressive cicatricial alopecia of the scalp, eyebrows and eyelashes. Additional findings can include photophobia, corneal dystrophy, facial erythema, and/or palmoplantar keratoderma.
- Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
- Synonyms: Keratosis follicularis spinulosa decalvans, Keratosis follicularis spinulosa decalvans cum ophiasi, Kfsdx
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