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Keratosis pilaris und Keratosis pilaris atrophicans faciei
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, 2006SummaryKeratosis 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. Ulerythema ophryogenes is an uncommon variant of keratosis pilaris characterized by erythematous follicular papules of the ...
Andreas W, Arnold, Stanislaw A, Buechner
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Archives of Dermatology, 1950
DURING the past fifteen years we have observed at the Pennhurst State School for feebleminded persons a group of patients exhibiting an asymptomatic follicular hyperkeratosis scattered diffusely over the dorsum of the trunk but usually without involvement of the extensor surfaces of the extremities.
F P, COOMBS, T, BUTTERWORTH
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DURING the past fifteen years we have observed at the Pennhurst State School for feebleminded persons a group of patients exhibiting an asymptomatic follicular hyperkeratosis scattered diffusely over the dorsum of the trunk but usually without involvement of the extensor surfaces of the extremities.
F P, COOMBS, T, BUTTERWORTH
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Journal of the American Academy of Dermatology, 2002
To the Editor: Although keratosis pilaris is mainly a cosmetic nuisance, it is often emotionally disturbing and difficult to treat. Urea, lactic acid, topical corticosteroids, topical and systemic retinoids, and other treatments have been used with varying success. Tazaroten selectively transactivates the retinoic acid receptors of the skin.
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To the Editor: Although keratosis pilaris is mainly a cosmetic nuisance, it is often emotionally disturbing and difficult to treat. Urea, lactic acid, topical corticosteroids, topical and systemic retinoids, and other treatments have been used with varying success. Tazaroten selectively transactivates the retinoic acid receptors of the skin.
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Keratosis pilaris decalvans non-atrophicans
Clinical and Experimental Dermatology, 1993A patient is described who presented with an eruption of tiny follicular keratotic papules on the limbs and the trunk accompanied by profuse hair loss. Histologically, a diagnosis of keratosis pilaris was made. The eruption cleared spontaneously in 3 months with complete regrowth of hair. Neither atrophy nor scarring remained.
DRAGO, FRANCESCO +3 more
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Natural history of keratosis pilaris
British Journal of Dermatology, 1994A questionnaire was sent to 83 patients in the south Buckinghamshire area, in whom a primary diagnosis of keratosis pilaris (KP) had been made within the preceding 20 years. Of the 50 questionnaires returned, one was invalid, and 49 were evaluated. The age range of patients surveyed was 18 months-25 years; 61% were female and 39% male.
L, Poskitt, J D, Wilkinson
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OIL CONTACT KERATOSIS PILARIS *
Australasian Journal of Dermatology, 1985SUMMARYA case is reported of a 55‐year‐old man of Greek origin who was employed by a bolt manufacturer. During the course of his work the patient was constantly in contact with cutting oil. He developed keratosis pilaris on the oil‐soaked areas. This is the first report of keratosis pilaris occurring as a reaction to contact with cutting oil in which ...
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2013
Keratosis pilaris atrophicans faciei (KPAF), also commonly known as ulerythema ophryogenes, is a rare disorder characterized by erythematous small keratotic papules that resolve with atrophy and resultant focal alopecia. This uncommon condition always involves the face, especially the eyebrows.
Omar Pacha, Adelaide Hebert
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Keratosis pilaris atrophicans faciei (KPAF), also commonly known as ulerythema ophryogenes, is a rare disorder characterized by erythematous small keratotic papules that resolve with atrophy and resultant focal alopecia. This uncommon condition always involves the face, especially the eyebrows.
Omar Pacha, Adelaide Hebert
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KERATOSIS PILARIS RUBRA ATROPHICANS FACIEI
Archives of Dermatology, 1948REPORT OF A CASE A WHITE girl, R. J., 16 years old, was first seen in July 1940. The condition of her skin had been present since early childhood and had not changed much. As shown in the genealogic chart, it was a hereditary condition and had resisted every type of treatment up to the time of examination.
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American family physician, 1978
This benign skin disorder is recognized by a characteristic appearance and a positive family history. Safe, effective treatment with urea creams and lotions is available.
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This benign skin disorder is recognized by a characteristic appearance and a positive family history. Safe, effective treatment with urea creams and lotions is available.
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