Results 11 to 20 of about 14,871 (251)

Keratosis follicularis spinulosa decalvans associated with acne keloidalis nuchae [PDF]

open access: diamond, 2014
Keratosis follicularis spinulosa decalvans (KFSD) is a keratinization disorder characterized by diffuse follicular hyperkeratosis, progressive cicatricial alopecia, corneal dystrophy, and photophobia. Acne keloidalis nuchae (AKN) is a syndrome of chronic
İlteriş Oğuz Topal   +3 more
core   +3 more sources

Keratosis follicularis spinulosa decalvans in a 15 months Cypriot girl

open access: diamondIndian Journal of Paediatric Dermatology, 2016
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   +3 more sources

Keratosis follicularis spinulosa decalvans

open access: diamondIndian Journal of Dermatology, Venereology, and Leprology, 2016
A 15-year-old boy, fifth child of a non-consanguineous marriage, presented to us with complaints of recurrent, raised, scaly, itchy lesions over the scalp of 7 years duration. Symptoms started 7 years back when his mother noticed some red, raised lesions
Anuj Bhatnagar   +3 more
semanticscholar   +3 more sources

Keratosis Follicularis Spinulosa Decalvans Associated With Woolly Hair: A Case Report. [PDF]

open access: yesCureus
Keratosis follicularis spinulosa decalvans X-linked (KFSDX) is part of the spectrum of a rare disorder known as keratosis pilaris atrophicans. Here, we report the case of a 14-year-old boy who presented with a history of abnormal hair since birth.
Brashi R   +5 more
europepmc   +2 more sources

Co-occurrence of erythrosis pigmentosa mediofacialis and erythromelanosis follicularis faciei et colli associated with keratosis pilaris in an adolescent female

open access: diamondIndian Journal of Dermatology, 2016
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

Darier-White Disease with Sensorineural Hearing Loss – A Case Report [PDF]

open access: yesRwanda Medical Journal, 2022
Darier-White disease (keratosis follicularis) is a rare autosomal dominant genodermatosis characterized by hyperkeratotic papules and plaques in seborrheic areas, often presenting with nail abnormalities and occasionally mucous membrane changes ...
E. B. Henshaw   +2 more
doaj   +4 more sources

KERATOSIS FOLLICULARIS SPINULOSA DECALVANS: REPORT OF A CASE AND LITERATURE REVIEW [PDF]

open access: greenActa Medica Iranica, 1999
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   +3 more sources

Molecular Pathogenesis and Complications Associated with Keratosis Follicularis: A Clinical Review [PDF]

open access: diamondSKIN The Journal of Cutaneous Medicine, 2021
Keratosis follicularis or Darier's disease (DD) is a rare autosomal dominant disorder characterized by the appearance of multiple scaly papules affecting seborrheic areas.
Hira Ghani   +3 more
openalex   +2 more sources

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