Results 121 to 130 of about 1,856 (171)
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Journal of Dermatology, 2016
AbstractDarier disease (DD) is a type of inherited keratinizing disorder that exhibits autosomal dominant inheritance. DD is caused by the mutations of ATP2A2, which encodes an endoplasmic reticulum calcium pump, sarco/endoplasmic reticulum ATPase type 2 (SERCA2).
exaly +3 more sources
AbstractDarier disease (DD) is a type of inherited keratinizing disorder that exhibits autosomal dominant inheritance. DD is caused by the mutations of ATP2A2, which encodes an endoplasmic reticulum calcium pump, sarco/endoplasmic reticulum ATPase type 2 (SERCA2).
exaly +3 more sources
British Journal of Dermatology, 2005
Darier's disease is a rare, dominantly inherited genodermatosis. Although it has been well studied in caucasians, very little is known about the clinical spectrum of this disorder among Asians.To determine the demographic and clinical profile of Asian patients with Darier's disease.This is a retrospective study of all new cases of Darier's disease seen
B K, Goh, P, Ang, C L, Goh
exaly +3 more sources
Darier's disease is a rare, dominantly inherited genodermatosis. Although it has been well studied in caucasians, very little is known about the clinical spectrum of this disorder among Asians.To determine the demographic and clinical profile of Asian patients with Darier's disease.This is a retrospective study of all new cases of Darier's disease seen
B K, Goh, P, Ang, C L, Goh
exaly +3 more sources
2018
Darier’s disease is an uncommon, autosomal-dominant inherited disorder. It is characterized by greasy, hyperkeratotic, skin-colored, or yellowish-brown papules that show a characteristic dermatoscopic pattern which consists of a central yellowish-brownish area of different morphologies (“star-like,” branched, polygonal, or roundish-oval), generally ...
Enzo Errichetti, Giuseppe Stinco
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Darier’s disease is an uncommon, autosomal-dominant inherited disorder. It is characterized by greasy, hyperkeratotic, skin-colored, or yellowish-brown papules that show a characteristic dermatoscopic pattern which consists of a central yellowish-brownish area of different morphologies (“star-like,” branched, polygonal, or roundish-oval), generally ...
Enzo Errichetti, Giuseppe Stinco
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Archives of Dermatology, 1964
Four cases of Darier's disease (keratosis follicularis) with unusual acral hemorrhagic lesions are presented and discussed. It is suggested that the lesions represent hemorrhage into lacunae secondary to trauma.
W N, JONES, T E, NIX, W H, CLARK
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Four cases of Darier's disease (keratosis follicularis) with unusual acral hemorrhagic lesions are presented and discussed. It is suggested that the lesions represent hemorrhage into lacunae secondary to trauma.
W N, JONES, T E, NIX, W H, CLARK
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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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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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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.
openaire +2 more sources