Atresia biliar: métodos diagnósticos extra-hepática da síndrome colestática do recém-nascido [thesis]. São Paulo: Faculdade de Medicina – USP; Atresia biliar extrahepática. Evoluciona hacia cirrosis precoz y ocasiona el fallecimiento antes de los 3 años de vida. Es la causa más frecuente. Statistics. Carta al Editor. Quiste de vía biliar tras portoenterostomía de Kasai en atresia de vías biliares extrahepáticas y su relación con colangitis de repetición.

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The magazine, referring to the Spanish-speaking pediatric, indexed in major international databases: You must be signed in to post a comment.

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Atresia biliar extra-hepática: métodos diagnósticos

The factor directly related with the mortality was the history of KP with an OR of 0. It is thought to affect 1 in 10, newborn infants. Check for errors and try again. Log in Sign up. Las infecciones virales pueden ser una posible causa. Please recommend JoVE to your librarian.

You can change the settings or obtain more information by clicking here. Edit article Share article View revision history. Fill out the form below to receive a free trial or learn more about access: The biliary atresia BA is the end result of a destructive and idiopathic inflammatory process affecting the intrahepatic and extrahepatic bile ducts, leading to fibrosis and biliary cirrhosis.

SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact. Synonyms or Alternate Spellings: Get cutting-edge science videos from J o VE sent straight to your inbox every month. KPthe age at delivery was 4.


SRJ is a prestige metric based on the idea that not all citations are the same. The Impact Factor measures the average number of citations received in a particular year by papers published in the journal during the two receding years.

[Prognostic factors related to mortality of children with atresia of bile ducts].

The prognosis of children with BA remains gloomy because they are diagnosed in late stages. The most important factor associated with mortality in these patients is to perform KP.

Luego, utilizando una pipeta de transferencia, recoger y guardar el suero para su uso posterior. Biliary atresia BA is a congenital biliary disorder, which is characterised by an absence or severe deficiency extrahepaticw the extrahepatic biliary tree.

When comparing the groups with and without KP, the lower age at the time of delivery, the age of diagnosis, a lower score on the PELD score and the Child-Pugh for the group with Kasai were statistically significant.

Please check your Internet connection and reload this page. Biliary atresia BA Atresia of the bile ducts. C este panel muestra la tasa de supervivencia biljar los ratones de cada grupo. A total of 66 patients with BA; 49 were girls Please sign in or create an account. National and foreign articles were also selected based on the bibliography of consulted publications, and when necessary, for better understanding of the theme, opinions emitted in theses and textbooks were referred.


We recommend downloading the newest version of Flash here, but we support all versions 10 and above. The objective was to identify factors associated with mortality in children with BA. You will only be able to see the first 20 seconds.

Among the complementary methods, the Biliag cholangiography, ultrasonography and hepatic biopsy should be used, depending on the technological resources of the diagnosis units. Fill out the form below to receive a free trial or learn more about access:.

[Prognostic factors related to mortality of children with atresia of bile ducts].

About Blog Go ad-free. Infants with biliary atresia may appear normal and healthy at birth. CiteScore measures average citations received per document published. To quiz yourself on this article, log in to see multiple choice questions.

A subscription to J o VE is required to view this article. Annals of Pediatrics is the Body of Scientific Expression of the Association and is the vehicle through which members communicate. The experience in England in relation to the “Yellow Alert” program, allowed that the number of children referred to surgical treatment before the 60 days of life increased significantly.

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