Results 181 to 190 of about 3,796 (217)
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International Journal of Dermatology, 2000
A 48‐year‐old Caucasian man recounted the onset of keratotic papules on the trunk at the age of 8 years, with subsequent spread to the forearms, scalp, and forehead. His most severe disease was present on the legs. He complained of pain, itching, and noted exacerbations in the summer and with sweating.
R, Katta, J, Reed, J E, Wolf
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A 48‐year‐old Caucasian man recounted the onset of keratotic papules on the trunk at the age of 8 years, with subsequent spread to the forearms, scalp, and forehead. His most severe disease was present on the legs. He complained of pain, itching, and noted exacerbations in the summer and with sweating.
R, Katta, J, Reed, J E, Wolf
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DARIER'S DISEASE OF THE LARYNX
Archives of Otolaryngology - Head and Neck Surgery, 1955DARIER'S disease is a rare but wellrecognized dermatologic disorder of unknown etiology characterized by papular, vesicular, and occasionally ulcerating lesions of the skin, particularly of the face, extremities, and inguinal region. Although it most frequently occurs in childhood, examples in infancy 1 as well as adulthood 2 have been recorded.
E R, FISHER, S L, KYLER
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British Journal of Dermatology, 1995
Darier's disease is an inherited disorder with well-recognized patterns of presentation. Lesions commonly affect the trunk and flexures. The diagnosis is based on the typical clinical appearance and histology showing acantholytic dyskeratosis. We report two unusual cases with prominent nodular, comedonal lesions on the face and scalp.
E K, Derrick, C R, Darley, S, Burge
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Darier's disease is an inherited disorder with well-recognized patterns of presentation. Lesions commonly affect the trunk and flexures. The diagnosis is based on the typical clinical appearance and histology showing acantholytic dyskeratosis. We report two unusual cases with prominent nodular, comedonal lesions on the face and scalp.
E K, Derrick, C R, Darley, S, Burge
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Archives of Dermatology, 1947
SINCE the first description by Darier 1 in 1889 more than three hundred and fifty papers have been published dealing with Darier's disease, a relatively rare condition, the cause of which, in spite of numerous investigations, remains undetermined. New knowledge of vitamin deficiency states brought promise of a fresh attack on the problem. Peck, Chargin
A D, PORTER, E W, GODDING, S R, BRUNAUER
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SINCE the first description by Darier 1 in 1889 more than three hundred and fifty papers have been published dealing with Darier's disease, a relatively rare condition, the cause of which, in spite of numerous investigations, remains undetermined. New knowledge of vitamin deficiency states brought promise of a fresh attack on the problem. Peck, Chargin
A D, PORTER, E W, GODDING, S R, BRUNAUER
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Darier's disease and psychosis
Psychiatry Research, 1996There are some reports in the literature about the comorbidity of Darier's Disease (keratosis follicularis) and psychiatric illness (e.g. mental retardation or affective disorders). Here we present evidence that schizophreniform psychosis may also be associated with Darier's Disease.
Hellwig, Bernhard +2 more
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International Journal of Dermatology, 1984
A 27‐year‐old, unmarried twin woman of the ethnic Malay presented with numerous tiny, firm, rough‐textured papules distributed symetrically over the faceb, neck, and chest for 13 years (Figs. 1 and 2) A few areas were covered with yellowish crusts and were slightly malodorous.
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A 27‐year‐old, unmarried twin woman of the ethnic Malay presented with numerous tiny, firm, rough‐textured papules distributed symetrically over the faceb, neck, and chest for 13 years (Figs. 1 and 2) A few areas were covered with yellowish crusts and were slightly malodorous.
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Dermatoglyphics in Darier's disease
British Journal of Dermatology, 1997Palmar and fingerprints were taken from 70 patients with Darier's disease and 409 normal controls. The dermatoglyphic characteristics of each group were determined and comparisons were made between them. Dermatoglyphic abnormalities were found; some confirmed previous findings and some were novel, but they are too small in degree and frequency to be of
D, Blackwell, S, Shuster
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Giornale italiano di dermatologia e venereologia : organo ufficiale, Societa italiana di dermatologia e sifilografia, 2016
[No abstract available]
BAHALI, Anil G. +6 more
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[No abstract available]
BAHALI, Anil G. +6 more
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Darier's (Darier–White) disease/keratosis follicularis
International Journal of Dermatology, 2004Darier’s (Darier–White) disease/keratosis follicularis was initially reported in the year 1889 by Darier and White independently. Darier’s disease has since (for over a century) fascinated research workers. 1–12 Almost all cases of the disease are attributed to mutations in the sarcoplasmic endoreticulum Ca 2+ -ATPase isoform-2 (SERCA-2).
Virendra N, Sehgal, Govind, Srivastava
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