Keratosis Pilaris Rubra Atrophicans Faciei

Hecht, Hugo

doi:10.1001/archderm.1948.01520200044005

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1964

2021

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Cited by 15 publications

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“…Although some individuals have had low serum vitamin A levels, oral and parenteral supplementation did not change the disease course (1,2,7,10), with one exception. Hecht (11) demonstrated moderate improvement using oral vitamin A and iron. However, return of the disease was noted after discontinuation.…”

Section: Discussionmentioning

confidence: 99%

Keratosis Pilaris Atrophicans: Case Series and Review

Callaway

Lesher

2004

Pediatric Dermatology

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Section: Discussionmentioning

confidence: 99%

Keratosis Pilaris Atrophicans: Case Series and Review

Callaway

Lesher

2004

Pediatric Dermatology

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Keratosis follicularis spinulosa decalvans. Report of two cases and literature review

Rand¹

1983

Archives of Dermatology

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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 pilaris with inflammation followed by atrophy. The clinical features and course of KFSD are characteristic. During infancy, keratosis pilaris begins on the face and, by childhood, progresses to involve the trunk and extremities. Sometime during childhood or up to the early teenage years, a cicatricial alopecia of the scalp and eyebrows develops and is the hallmark of this disorder. Hyperkeratosis of the palms and soles is a frequently associated finding and is usually manifested during adolescence. Other features occurring with this syndrome include atopy, photophobia, and corneal abnormalities. Sex-linked inheritance has been proposed by several authors.

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Ulerythema Ophryogenes

Davenport¹

1964

Arch Dermatol

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Keratosis Pilaris Rubra Atrophicans Faciei

Cited by 15 publications

References 2 publications

Keratosis Pilaris Atrophicans: Case Series and Review

Keratosis Pilaris Atrophicans: Case Series and Review

Keratosis follicularis spinulosa decalvans. Report of two cases and literature review

Ulerythema Ophryogenes

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