EPIDERMOLISIS AMPOLLAR SIMPLE PDF

Dijinn Summary and related texts. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a ismple for diagnosis or treatment. Both hyper- and hypopigmentation can occur, typically in areas of blistering. As a result, severe forms of the disease may be fatal. Recommendations for the evaluation of parents of a proband with an apparent de novo pathogenic variant include taking a personal history and performing a physical examination if the history epidermoliis suggestive.

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Milabar SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field. This was a descriptive, cross-sectional chart-review study in which we recorded the type and main subtypes of EB and the presence or absence of DC.

You can change the settings or obtain more information by clicking here. Previous article Next article. Periodic follow-up should be performed to make an early diagnosis and start treatment. Read this article in English. Go to the members area of the website of the AEDV, https: DC is typically in an advanced phase when detected, leading to a poorer prognosis.

Results Fifty-seven patients with EB were found, 19 with EB simplex, 10 with junctional EB, 27 with dystrophic EB 14 dominant dystrophic and 13 recessive dystrophicand just 1 with Kindler syndrome. Introduction and objective In recent decades, an association has been reported between epidermolysis bullosa EB and dilated cardiomyopathy DC.

This item has received. Epidermolysis bullosa simplex, Kobner Twenty-three patients had presented factors that could have had a causal relationship with the potential onset of DC. Methods This was a descriptive, cross-sectional chart-review study in which we recorded the type and main subtypes of EB and the presence or absence of DC. Subscribe to our Newsletter. Si continua navegando, consideramos que acepta su uso. CiteScore measures average citations received per document published.

Twenty-three patients had presented factors that could have had a causal relationship with the potential onset of DC. Fifty-seven patients with EB were found, 19 with EB simplex, 10 with junctional EB, 27 with dystrophic EB 14 dominant dystrophic and 13 recessive dystrophicand just 1 with Kindler syndrome.

Subscriber If you already have your login data, please click here. Continuing navigation will be considered as acceptance of this use. SRJ is a prestige metric based on the idea that not all citations are the same. In recent decades, an association has been reported between epidermolysis bullosa EB and dilated cardiomyopathy DC.

DC was detected in only 2 patients with recessive dystrophic EB. All articles are subjected to a rigorous process of revision in pairs, and careful editing for literary and scientific style.

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Epidermólisis ampollar

Methods This was a descriptive, cross-sectional chart-review study in which we recorded the type and main subtypes of EB and the presence or absence of DC. DC is typically in an advanced phase when detected, leading to a poorer prognosis. CiteScore measures average citations received per document published. This item eipdermolisis received. Go to the members area of the website of the AEDV, https: All articles are subjected to a rigorous process of revision in pairs, and careful editing for literary and scientific style.

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EPIDERMOLISIS AMPOLLAR SIMPLE PDF

Previous article Next article. Pemphigus Vegetans in the Inguinal Folds. Show more Show less. DC was detected in only 2 patients with recessive dystrophic EB. C — Generalized epidermolysis bullosa simplex Are you a health skmple able to prescribe or dispense drugs?

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