Fibrosis hepática congénita y enfermedad poliquística renal autosómica recesiva . Author links open overlay érrez Junquera Fibrosis hepática congénita y enfermedad poliquística renal autosómica recesiva . Article in Anales de Pediatría 52(5) · December with 3 Reads. La enfermedad renal poliquística (PKD, por su sigla en inglés) es una enfermedad genética . Durán-Álvarez S. Enfermedad poliquística autosómica recesiva.

Author: Shaktilkis Doushicage
Country: Ecuador
Language: English (Spanish)
Genre: Video
Published (Last): 27 May 2007
Pages: 213
PDF File Size: 8.46 Mb
ePub File Size: 13.91 Mb
ISBN: 904-3-35564-374-8
Downloads: 87049
Price: Free* [*Free Regsitration Required]
Uploader: Gabar

Annals of Pediatrics is the Body of Scientific Expression of the Association and is the vehicle through which members communicate. Introduction Autosomal recessive polycystic kidney disease ARPKD is a genetic disorder caused by a mutation in the PKD1 gene, which codes for protein polycystin 1, mapped on chromosome 6p Recomendaciones del Grupo de Trabajo de Obesidad de la Are you a health professional able to prescribe or dispense drugs?

Polycystic disease of kidney presenting in childhood. Si continua navegando, consideramos que acepta su uso.

File:Enfermedad poliquística renal autosómica – Wikimedia Commons

De la Rubia, M. Poliqquistica a one stop shop for users enfermedsd OA Journals. 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. To present a brief account of the most relevant aspects of kidney disease: All autosomal polycystic kidney disease patients with stage 5 chronic kidney disease should be considered for transplantation, since it is not contraindicated in most cases. Scopus is a bibliographic database publishing summaries and references concerning articles from scientific journals.


Directory of Open Access Journals DOAJ increases the visibility and ease of use of open access scientific and scholarly journals, aims to be comprehensive and cover all that journals that use a quality control system to guarantee the content.

Combined cystic disease of the liver and kidney. To improve our services and products, we use “cookies” own or third parties authorized to show advertising related to client preferences through the analyses of navigation customer behavior.

Pregnancy in autosomal recessive polycystic kidney disease. These disease presents in two forms, which can be differentiated by their inheritance patterns: Autosomal Dominant Polycystic Kidney Disease.

Scopus Scopus is a bibliographic database publishing summaries and references concerning articles from scientific journals. ARPKD is characterised by the formation of cysts from coalescing dilated renal collecting ducts coexisting with congenital hepatic fibrosis secondary to biliar dysgenesis.

File:Enfermedad poliquística renal autosómica recesiva.jpg

Get a more complete global picture by discovering new insights from research in Latin America, Spain, Portugal, the Caribbean and South Africa. Latindex is the product of cooperation by a network of Latin-American institutions operating in enfermedwd coordinated way to gather and disseminate bibliographic information about serialised scientific publications produced in the region.

The magazine, referring to the Spanish-speaking pediatric, indexed in major international databases: Ludwig symposium on biliary disorders – part I.

J Med Genet, 8pp. Clin Nucl Med, 18pp.



Everolimus in patients with autosomal dominant polycystic kidney disease. Autosomal dominant polycystic kidney disease. Chapman AB, Wei W. Hospital General de Albacete. Hypertension in autosomal dominant polycystic kidney disease. Defective glucose metabolism in polycystic kidney disease identifies a new therapeutic strategy. It is currently being managed in Colombia by the Universidad Nacional de Colombia. Semin Liv Dis, 14pp. I, autosommica copyright holder of this work, release this work into the public domain.

Hospital General de Albacete. Semin Liv Dis, 14pp. The pregnancy had not been monitored, although a previous ultrasonography revealed foetal kidney enlargement. Ludwig symposium on biliary poliquisstica – part I.

Si continua navegando, consideramos enfemedad acepta recewiva uso. Polycystic kidney disease PKD is a common genetic disease in which cystic lesions develop and progressively replace the renal parenchyma.

Renal artery embolization for the symptomatic treatment of adult polycystic kidney disease. Gross pathology of polycystic kidney disease.

IBN Publindex Publindex is a Colombian bibliographic index for classifying, updating, rating and certifying scientific and technological publications. This item has received.

The most significant macroscopic findings were sponge kidneys composed of multiple small cysts and focal hepatic fibrosis. Human Genet, 68pp.