EPIDERMOLISIS AMPOLLOSA DISTROFICA PDF

Suele asociarse a epidermólisis ampollosa distrófica dominante. La epidermólisis ampollosa juncional tipo Herlitz es una variante rara, habitualmente mortal. Epidermolysis bullosa is a group of genetic conditions that cause the skin to be very fragile and to blister easily. Blisters and skin erosions form in response to. A number sign (#) is used with this entry because autosomal recessive dystrophic epidermolysis bullosa (RDEB) and the RDEB localisata variant are caused by.

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OMIM Entry – # – EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE; RDEB

In the year has been indexed in the Medlinedatabase, and has become a vehicle for expressing the most current Spanish medicine and modern. All articles are subjected to a rigorous process of revision in pairs, and careful editing for literary and scientific style. CiteScore measures average citations received per document published.

SRJ is a prestige metric based on the idea that not all citations are the same. SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact.

SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field. In recent decades, an association has been reported between epidermolysis bullosa EB and dilated cardiomyopathy DC.

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DC is typically in an advanced phase when detected, leading to a poorer prognosis. 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.

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. DC was detected in only 2 patients with recessive dystrophic EB.

Twenty-three patients epidermlisis presented factors that could have had a causal relationship with the potential onset of DC. Periodic follow-up should be performed to make an early diagnosis and start treatment.

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Show more Show less. Introduction and objective In recent decades, an distroffica has been reported between epidermolysis bullosa EB and dilated cardiomyopathy 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. 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.

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Twenty-three patients had presented factors that could have had a causal relationship with the potential onset of DC. Periodic follow-up should epiedrmolisis performed to make an early diagnosis and start treatment.

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