ENFERMEDAD DE DOWLING-DEGOS PDF

Dowling-Degos disease is characterized by a lacy or net-like reticulate pattern of abnormally dark skin coloring hyperpigmentation , particularly in the body's folds and creases. These skin changes typically first appear in the armpits and groin area and can later spread to other skin folds such as the crook of the elbow and back of the knee. Less commonly, pigmentation changes can also occur on the wrist, back of the hand, face, scalp, scrotum in males , and vulva in females. Individuals with Dowling-Degos disease may also have dark lesions on the face and back that resemble blackheads, red bumps around the mouth that resemble acne, or depressed or pitted scars on the face similar to acne scars but with no history of acne. Cysts within the hair follicle pilar cysts may develop, most commonly on the scalp.

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Key words:. Enfermedad de Dowling-Degos. Dermatol Rev Mex ; Enfermedad de Dowling- Degos. Actas Dermosifiliogr ; Rev Cent Dermatol Pascua ; A heterozygous frameshift mutation in the V1 domain of keratin 5 in a family with Dowling-Degos disease. J Invest Dermatol ; Derm Venez ; Am J Hum Genet ; Degos R, Ossipowski B. Ann Dermatol Syphiligr ; Loss-offunction mutations in the keratin 5 gene lead to Dowling- Degos disease.

Type 1 segmental Galli-Galli disease resulting from a previously unreported keratin 5 mutation. A gene locus responsible for reticulate pigmented anomaly of the flexures maps to chromosome 17p J Invest Dermatol ; Unique brown star shape on dermatoscopy of generalized Dowling- Degos disease. Australas J Dermatol ; Wititsuwannakul J, Noppakun N. Generalized Dowling-Degos disease: case reports. Ann Dermatol ; Enfermedad de Dowling-Degos asociada con carcinoma basocelular.

Dermatol Peruan ; Dowling-Degos disease and hidradenitis suppurativa: Co occurrence or association? Indian Dermatol Online J ; Hidradenitis suppurativa, Dowling-Degos and multiple epidermal cysts: a new follicular occlusion triad. Clin Exp Dermatol ; Dowling-Degos disease: classic clinical and histopathological presentation.

An Bras Dermatol ; Dowling-Degos disease: case report and review of the literature. Dermatology ; Wholeexome sequencing identifies ADAM10 mutations as a cause of reticulate acropigmentation of Kitamura, a clinical entity distinct from Dowling-Degos disease.

Hum Mol Genet ; J Cosmet Laser Ther ; Follicular Dowling- Degos disease: A rare variant of an evolving dermatosis. Indian J Dermatol Venereol Leprol ; Presentation of reticulate acropigmentation of Kitamura and Dowling-Degos disease overlap. J Clin Aesthet Dermatol ; Dowling-Degos disease involving the vulva and back: case report and review of the literature. Dermatol Online J ; Three cases of Dowling Degos disease in two families. Indian J Dermatol Venereol Leprol ; Kawaguchi M, Hearing VJ.

The roles of ADAMs family proteinases in skin diseases. Enzyme Res ; A case of reticulate acropigmentation of Kitamura: Dowling-Degos disease overlap with unusual clinical manifestations. Indian J Dermatol ; Genome-wide linkage, exome sequencing and functional analyses identify ABCB6 as the pathogenic gene of dyschromatosis universalis hereditaria. PLoS One ; Discromatosis hereditaria universal: relato de un caso.

Dermatol Pediatr Lat ; Five novel mutations in the ADAR1 gene associated with dyschromatosis symmetrica hereditaria. BMC Med Genet ; Dyschromatosis symmetrica hereditaria of late onset? Case Rep Dermatol Med ; Papilomatosis confluente y reticulada. Arch Argent Dermatol ; Familial confluent and reticulated papillomatosis. Arch Dermatol ; KRT14 haploinsufficiency results in increased susceptibility of keratinocytes to TNF-alpha-induced apoptosis and causes Naegeli-Franceschetti-Jadassohn syndrome.

Itin PH, Burger B. Spontaneous fading of reticular pigmentation in Naegeli-Franceschetti-Jadassohn syndrome. Naegeli-Franceschetti-Jadassohn syndrome and dermatopathia pigmentosa reticularis: two allelic ectodermal dysplasias caused by dominant mutations in KRT Fifty-four novel mutations in the NF1 gene and integrated analyses of the mutations that modulate splicing.

Int J Mol Med ; Millikan LE. Adapalene: an update on newer comparative studies between the various retinoids. Int J of Dermatol ; Dermatol Surg ; Full text How to cite this article. Key words: Dowling-Degos disease, keratin 5, protein O-fucosyltransferase 1, protein O-glucosyltransferase 1, Galli-Galli disease.

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Dermatology Online Journal

Key words:. Enfermedad de Dowling-Degos. Dermatol Rev Mex ; Enfermedad de Dowling- Degos. Actas Dermosifiliogr ;

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2014, Number 6

Skip to search form Skip to main content You are currently offline. Some features of the site may not work correctly. Dowling-Degos disease DDD or reticular pigmented anomaly of the flexures is a rare autosomal dominant genodermatosis with variable penetrance. It mainly affects young women and is characterized by acquired reticular hyperpigmentation of the large skin folds. View PDF.

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Dowling-Degos disease

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