ENFERMEDAD RENAL POLIQUISTICA AUTOSOMICA DOMINANTE PDF

ECG bpm. Genética Progresiva Quistes de diferentes tamaños 60 años –> Insuficiencia Renal Autosomica dominante. Clasificación en. Antecedente familiar; Presencia al menos 2 quistes renales en uno o ambos lados ( años); Dos quistes en cada riñon ( años). Autosómica Dominante/ Recesiva Enfermedad Poliquística Renal. Trastorno multisistémico caracterizado por múltiples quistes renales.

Author: Grolmaran Zulumi
Country: Italy
Language: English (Spanish)
Genre: Photos
Published (Last): 22 December 2010
Pages: 301
PDF File Size: 14.37 Mb
ePub File Size: 4.71 Mb
ISBN: 944-4-94808-808-8
Downloads: 43956
Price: Free* [*Free Regsitration Required]
Uploader: Maum

Autosomal dominant polycystic kidney disease | Radiology Reference Article |

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 nefermedad.

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 ARPKD is characterised by the formation of cysts from coalescing dilated renal collecting ducts coexisting with domibante hepatic fibrosis secondary to biliar dysgenesis.

  CONECTADOS EN EL CIBERESPACIO ROBERTO APARICI PDF

poliquistiica We report the autopsy findings in a 2 h old, term female infant with severe oligohydramnios. The pregnancy had not been monitored, although a previous ultrasonography revealed foetal kidney enlargement.

The most significant macroscopic findings were sponge kidneys composed of multiple small cysts and focal hepatic fibrosis. Microscopically a diagnosis of autosomal recessive polycystic kidney disease with biliary dysgenesis was made.

The clinical and pathological findings are correlated and the most important necropsy findings are described. The relevant literature autosomoca reviewed and recent advances in the pathology, genetics, diagnosis, ultrasonography, prevention and treatment of ARPKD are discussed.

Previous article Next article. January – March Pages Autosomal recessive polycystic kidney disease. This item has received. Show more Show less.

Enfermedad poliquistica renal by Melissa Gastelum on Prezi Next

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 ARPKD is characterised by the formation of cysts from coalescing dilated renal collecting ducts coexisting with congenital hepatic fibrosis secondary to biliar dysgenesis.

Case report We report the autopsy findings in a 2 h old, term female infant with severe oligohydramnios. Microscopically a diagnosis of autosomal recessive polycystic kidney disease with biliary dysgenesis was made. Discussion The clinical and pathological findings are correlated and domjnante most important necropsy findings are described.

  INSTRUKCJA SUBIEKT GT PDF

The relevant literature is reviewed and recent advances in the pathology, genetics, diagnosis, ultrasonography, prevention and treatment of ARPKD are discussed.

Subscriber If you already have your login data, please click here. From Monday to Friday from 9 a. Subscribe to our Newsletter.

Print Send to a friend Export reference Mendeley Statistics. Iodine seeds in prostatic transurethral resection Pulmonary cysts in smoking-related interstitial fibrosis: Si continua navegando, consideramos que acepta su uso.

ENFERMEDAD RENAL POLIQUISTICA EBOOK

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. Continuing navigation will be considered as acceptance of this use.

You can change the settings or obtain more information by clicking here. Se renak a navegar, consideramos que aceita o seu uso. Are you a health professional able to prescribe or dispense drugs?