Keratosis follicularis spinulosa decalvans (KFSD) is a rare, inherited, skin disorder. KFSD is characterized by hardening of the skin (keratosis) on several parts of the body.

Keratosis follicularis spinulosa decalvans is a rare genodermatosis occurring during infancy or childhood, predominantly affecting males, and characterized by diffuse follicular …

Keratosis follicularis spinulosa decalvans is a disorder affecting the hair follicles characterized by scarring alopecia of the scalp, eyebrows, and axillae, sometimes associated with photophobia …

Keratosis follicularis spinulosa decalvans (KFSD) is an X-linked xenodermatosis characterized by scarring alopecia and follicular hyperkeratosis. This condition mainly affects males with …

• We report herein two cases of keratosis follicularis spinulosa decalvans (KFSD) and review the literature on this condition. The entity is one of a group of related disorders that shows …

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 …

Keratosis Follicularis Spinulosa Decalvans is a rare genetic disorder that affects the hair follicles and skin. The types of Keratosis Follicularis Spinulosa Decalvans include classical KFSD, …

Keratosis follicularis spinulosa decalvans (KFSD) is an uncommon inherited skin condition. Most cases are found in men. Females who have the disease tend to have milder symptoms. KFSD …

Keratosis follicularis spinulosa decalvans (KFSD) is a rare, inherited, skin condition. KFSD is a form of ichthyoses, a group of inherited conditions of the skin in which the skin tends to be …

Keratosis Follicularis Spinulosa Decalvans (KFSD) is a skin disorder that is believed to be an X-linked genetic condition, since a majority of the individuals affected are males. It develops …