KERATOSIS FOLLICULARIS SPINULOSA DECALVANS: REPORT OF A CASE AND LITERATURE REVIEW [PDF]
Keratosis follicularis spinulosa decalvans (KFSD) represents a rare, probably X-linked recessive genodermatosis, characterized by keratosis pilaris of face, trunk and extremities, followed by atrophy, cicatricial alopecia of the scalp, eyebrows and ...
P. Mansouri. +1 more
doaj +4 more sources
Keratosis follicularis spinulosa decalvans in a 15 months Cypriot girl [PDF]
Keratosis follicularis spinulosa decalvans (KFSD) is a rare disease with unknown etiology. It clinically presents with diffuse follicular hyperkeratosis of scalp which progress to atrophy, cicatricial alopecia, and photophobia.
Asli Kaptanoglu +2 more
doaj +2 more sources
Co-occurrence of erythrosis pigmentosa mediofacialis and erythromelanosis follicularis faciei et colli associated with keratosis pilaris in an adolescent female [PDF]
Erythromelanosis follicularis faciei et colli (EFFC) is a rare disease characterized by a triad of reddish-brown pigmentation, erythema and follicular papules localized on face and neck and is usually described in males.
Sarita Kalwaniya +3 more
doaj +2 more sources
Lichen Planus Follicularis Tumidus of the Vulva: A Case Report and Literature Review
Lichen planus follicularis tumidus (LPFT) is a rare variant of follicular lichen planus that predominantly affects the postauricular region, although cases involving the nasal ala and vulva have also been reported.
Kong Xiangjun +4 more
doaj +2 more sources
Keratosis follicularis spinulosa [PDF]
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core +8 more sources
Keratosis follicularis is a genetic disorder that is inherited in an autosomal dominant pattern. Physical examination classically shows keratotic papules that are distributed mostly on the so-called "seborrheic" areas of the body. Nail involvement is not uncommon and is characterized by V-shaped nicking at the distal aspect of the nail bed ...
Kosann, Meredith K, +1 more
openaire +5 more sources
The Role of Trichoscopy in Keratosis Follicularis Spinulosa Decalvans: Case Report and Review of the Literature. [PDF]
Keratosis follicularis spinulosa decalvans (KFSD) is a rare, X-linked, hereditary disorder of keratinization, characterized by skin involvement and progressive scarring alopecia of scalp, eyebrows, and eyelashes. The diagnosis is helped by the particular
Alessandrini A +4 more
europepmc +2 more sources
Eine neuartige MBTPS2‐Missense‐Variante identifiziert Keratosis follicularis spinulosa decalvans in einem Fall von neonataler Erythrodermie [PDF]
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 24, Issue 3, Page 392-397, March 2026.
Cuperus E +7 more
europepmc +2 more sources
The Girl with a Pearl Earring: A dermatological puzzle. [PDF]
Journal of the European Academy of Dermatology and Venereology, Volume 39, Issue 12, Page 2037-2038, December 2025.
Girolomoni G, Gisondi P, Maurelli M.
europepmc +2 more sources

