Results 191 to 200 of about 14,871 (251)
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Keratosis follicularis spinulosa decalvans in a woman with XY karyotype
International Journal of Dermatology, 2022the back, therefore, we do not consider it to be pathogenic. The eruption tends to persist from a few months to 90 months. The optimal treatment of NSA is unknown.
Rubén Linares-Navarro +2 more
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Successful Treatment of Keratosis Follicularis Spinulosa Decalvans With an 800-nm Diode Laser.
Dermatologic Surgery, 2020Keratosis follicularis spinulosa decalvans (KFSD) is a rare genodermatosis characterized by widespread keratosis pilaris and progressive cicatricial alopecia of the scalp, eyebrows, and eyelashes; photophobia; and corneal dystrophy.
B. Bhoyrul, R. Sinclair
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Reflectance confocal microscopy in keratosis follicularis squamosa
Skin research and technology, 2020Dear Editor, First described by Dohi and Momose in 1903, keratosis follicularis squamosa (KFS) is a rare disorder of follicular keratinization, which is well recognized in Japan but rarely reported in China.1 It appears clinically as scaly patches up to ...
Xiaopo Wang, Jianfang Sun
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Keratosis follicularis spinulosa decalvans
Der Hautarzt, 2007Keratosis follicularis spinulosa decalvans is a rare, X-linked disorder of keratinization of the hair follicle with inflammation and atrophy associated with corneal dystrophy and other symptoms. A family with several affected members is reported. The unaffected parents were related.
D, Helbig, S, Grabbe, T, Jansen
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Observations on Keratosis Follicularis
Archives of Dermatology, 1960Keratosis follicularis, commonly referred to as Darier's disease, is a rare, persistent, cutaneous disorder characterized by malodorous, greasy, crusted, sometimes pustular, hyperkeratotic brownish-red papules located primarily on the scalp, face, retroauricular areas and the trunk.
J N, PENROD +2 more
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Novel mutation in MBTPS2 causes keratosis follicularis spinulosa decalvans in a large Chinese family
International Journal of Dermatology, 2018Keratosis follicularis spinulosa decalvans (KFSD; OMIM 308800) is a rare genetic disorder characterized by a peculiar triad of keratotic follicular papules and progressive alopecia of the scalp, eyelashes, and eyebrows.
Chong Chen +4 more
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Archives of Dermatology and Syphilology, 1943
In 1938 Peck 1 studied a case of Darier's disease in a man aged 25. It occurred to him that since the chief pathologic change is a follicular dyskeratosis, the disease might possibly be due to vitamin A deficiency. He therefore tried the effect of large doses of this vitamin and obtained considerable clinical improvement.
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In 1938 Peck 1 studied a case of Darier's disease in a man aged 25. It occurred to him that since the chief pathologic change is a follicular dyskeratosis, the disease might possibly be due to vitamin A deficiency. He therefore tried the effect of large doses of this vitamin and obtained considerable clinical improvement.
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EJD. European journal of dermatology, 2019
of urticarial reactions, with infliximab were negative on immediate and two-day readings (prick tests and intradermoreaction [IDR]: 0.02 mg/mL, 0.2 mg/mL and 2 mg/mL).
Y. Nakamura +8 more
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of urticarial reactions, with infliximab were negative on immediate and two-day readings (prick tests and intradermoreaction [IDR]: 0.02 mg/mL, 0.2 mg/mL and 2 mg/mL).
Y. Nakamura +8 more
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Unilateral Keratosis Follicularis
Archives of Dermatology, 1977To the Editor.— Keratosis follicularis (Darier's disease) usually presents as a symmetrical eruption of keratotic, often greasy, follicular and perifollicular papules. Sites of predilection are the chest, upper back, extremities, scalp, and inguinal area. It is thought to be transmitted as an autosomal dominant with incomplete penetrance.
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Clincal and Experimental Dermatology, 2022
A. Murad, Wilma F. Bergfeld
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A. Murad, Wilma F. Bergfeld
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