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Page 1
Treatment of keratosis pilaris and its variants: a systematic review.
Maghfour J, Ly S, Haidari W, Taylor SL, Feldman SR. Maghfour J, et al. J Dermatolog Treat. 2022 May;33(3):1231-1242. doi: 10.1080/09546634.2020.1818678. Epub 2020 Sep 14. J Dermatolog Treat. 2022. PMID: 32886029 Review.
INTRODUCTION: Keratosis pilaris (KP) is a common, benign skin condition of follicular hyperkeratosis. ...
INTRODUCTION: Keratosis pilaris (KP) is a common, benign skin condition of follicular hyperkeratosis. ...
Keratosis pilaris: an update and approach to management.
Kodali N, Patel VM, Schwartz RA. Kodali N, et al. Ital J Dermatol Venerol. 2023 Jun;158(3):217-223. doi: 10.23736/S2784-8671.23.07594-1. Epub 2023 May 11. Ital J Dermatol Venerol. 2023. PMID: 37166753 Free article. Review.
Keratosis pilaris (KP) is a common, hyperkeratotic skin condition characterized by small, folliculocentric papules with variable perifollicular erythema. ...KP represents a family of follicular disorders, of which KP simplex is by far the most common. Other variants
Keratosis pilaris (KP) is a common, hyperkeratotic skin condition characterized by small, folliculocentric papules with variab
Keratosis Pilaris and its Subtypes: Associations, New Molecular and Pharmacologic Etiologies, and Therapeutic Options.
Wang JF, Orlow SJ. Wang JF, et al. Am J Clin Dermatol. 2018 Oct;19(5):733-757. doi: 10.1007/s40257-018-0368-3. Am J Clin Dermatol. 2018. PMID: 30043128 Review.
Keratosis pilaris is a common skin disorder comprising less common variants and rare subtypes, including keratosis pilaris rubra, erythromelanosis follicularis faciei et colli, and the spectrum of keratosis pilaris atrophicans. ...
Keratosis pilaris is a common skin disorder comprising less common variants and rare subtypes, including keratosis p
Keratosis pilaris: a common follicular hyperkeratosis.
Hwang S, Schwartz RA. Hwang S, et al. Cutis. 2008 Sep;82(3):177-80. Cutis. 2008. PMID: 18856156 Review.
Keratosis pilaris (KP) is a common inherited disorder of follicular hyperkeratosis It is characterized by small, folliculocentric keratotic papules that may have surrounding erythema. ...When diagnosing KP, the clinician should be aware that a number of diseases are
Keratosis pilaris (KP) is a common inherited disorder of follicular hyperkeratosis It is characterized by small, folliculocent
Trias of keratosis pilaris, ulerythema ophryogenes and 18p monosomy: Zouboulis syndrome.
Liakou AI, Esteves de Carvalho AV, Nazarenko LP. Liakou AI, et al. J Dermatol. 2014 May;41(5):371-6. doi: 10.1111/1346-8138.12442. J Dermatol. 2014. PMID: 24801913 Review.
Keratosis pilaris and ulerythema ophryogenes (keratosis pilaris atrophicans faciei) are part of a group of hereditary disorders of hair follicle keratinization involving follicular inflammation and subsequent atrophy. ...We have reviewed the fiv
Keratosis pilaris and ulerythema ophryogenes (keratosis pilaris atrophicans faciei) are part of a group o
Atrophoderma vermiculatum: a case report and review of the literature on keratosis pilaris atrophicans.
Luria RB, Conologue T. Luria RB, et al. Cutis. 2009 Feb;83(2):83-6. Cutis. 2009. PMID: 19326693 Review.
Atrophoderma vermiculatum (AV) is a rare follicular disorder primarily affecting children with reticular or honeycomb atrophy of the cheeks and forehead. Along with keratosis pilaris atrophicans faciei (KPAF) and keratosis follicularis spinulosa decalvans (KF …
Atrophoderma vermiculatum (AV) is a rare follicular disorder primarily affecting children with reticular or honeycomb atrophy of the cheeks …
[Keratosis pilaris and keratosis pilaris atrophicans faciei].
Arnold AW, Buechner SA. Arnold AW, et al. J Dtsch Dermatol Ges. 2006 Apr;4(4):319-23. doi: 10.1111/j.1610-0387.2006.05933.x. J Dtsch Dermatol Ges. 2006. PMID: 16638061 Review. German.
Keratosis pilaris and ulerythema ophryogenes (keratosis pilaris atrophicans faciei) are hereditary disorders with altered follicular keratinization that show follicular, horny papules surrounded by an erythematous halo. ...On the background of 1
Keratosis pilaris and ulerythema ophryogenes (keratosis pilaris atrophicans faciei) are hereditary disord
Skin manifestations of cardio-facio-cutaneous syndrome.
Borradori L, Blanchet-Bardon C. Borradori L, et al. J Am Acad Dermatol. 1993 May;28(5 Pt 2):815-9. doi: 10.1016/0190-9622(93)70108-6. J Am Acad Dermatol. 1993. PMID: 8491871 Review.
Our two patients had many of the cardinal features of the disorder: a peculiar craniofacial appearance with sparse curly hair, low-set posteriorly rotated ears, moderate to severe mental retardation, heart defects, and cutaneous abnormalities such as ichthyosis, widespread ker
Our two patients had many of the cardinal features of the disorder: a peculiar craniofacial appearance with sparse curly hair, low-set poste …
Ulerythema ophryogenes, a rarely reported cutaneous manifestation of noonan syndrome: case report and review of the literature.
Li K, Ann Thomas M, Haber RM. Li K, et al. J Cutan Med Surg. 2013 May-Jun;17(3):212-8. doi: 10.2310/7750.2011.11017. J Cutan Med Surg. 2013. PMID: 23673306 Review.
BACKGROUND: Ulerythema ophryogenes (also known as keratosis pilaris atrophicans faciei) is a rarely reported cutaneous manifestation of Noonan syndrome. ...
BACKGROUND: Ulerythema ophryogenes (also known as keratosis pilaris atrophicans faciei) is a rarely reported cutaneous …
11 results