ENFERMEDAD DE DARIER PDF

La enfermedad de Darier es una genodermatosis caracterizada por queratinización tegumentaria particular, más frecuente en la 2.a–3.a décadas de la vida. La disqueratosis folicular (enfermedad de Darier-White) es un trastorno infrecuente autosómico dominante en el que se produce una queratinización alterada. A rule concerning the segmental manifestation of autosomal dominant skin disorders: Review of clinical examples providing evidence for dichotomous types of.

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CiteScore measures average citations received per document published. Darier disease with paired segmental mani-festation of either excessive or absent involvement. Go to the members area of the website of the AEDV, https: The disease has a variety of manifestations and lacks consistent genotype—phenotype correlations.

In the year has been indexed in the Medlinedatabase, and darire become a vehicle for expressing the most current Spanish medicine and modern. Acantholytic dyske-ratotic epidermal nevus: Subscriber If you already have your login data, please click here. Previous article Next article. Variant cutaneous phenotypes associated with misense mutations, but neuropsychiatric features are independent of mutation class.

Enfermedad de Darier unilateral y segmentaria de tipo 1 | Anales de Pediatría

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Show more Show less. You can change the settings or obtain more information by clicking here. Continuing navigation will be considered as acceptance of this use. Other classic signs of the disease may be present in the same patient or relatives. Nat Genet, 21pp.

Enfermedad de Darier segmentaria | Actas Dermo-Sifiliográficas (English Edition)

SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field. March Pages Continuing navigation will be considered as acceptance of this use.

CiteScore measures average citations received per document published. Histologically, suprabasal acantholysis and abundant dyskeratotic cells were seen.

May Pages Print Send to a friend Export reference Mendeley Statistics. SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact. Acral Hemorrhagic Darier Disease. Si continua navegando, consideramos que acepta su uso. ATP2A2 mutations in Darier’s disease. We present daier case of Darier’s disease in a young man, with a 3 year clinical history of skin lesions but no family history of this condition.

Reportamos 3 nuevos casos de esta variante desencadenados por traumatismo y evidenciando buena respuesta con retinoides. Implications for genetic studies.

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All articles are subjected to a rigorous process of revision in pairs, and careful editing for literary and scientific style. You can change the settings or obtain more information by clicking here. Subscriber If you already have your login data, please click here.

Go to the members area of the website of the AEDV, https: If you are a member of the AEDV: Review of clinical examples providing evidence for dichotomous types of severity. Hum Mol Genet, 8pp. Show more Show less.

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From Monday to Friday from 9 a. Histopathology reveals dyskeratosis and suprabasal acantholysis with hemorrhagic lacunae. Si continua navegando, consideramos que acepta su uso. If you are a member of the AEDV: Subscriber If you already have your login data, please click here.

SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field.