Tables v. KDIGO Board Members vi. Reference Keys vii. Abbreviations and Acronyms viiii. Notice. Foreword. Work Group Membership. Abstract. Glomerulopatias en pediatria. Year: Month: June. Date: June 17, to June 18, Location: Asuncion, Paraguay. Course director: Diana Baez de. 10 Oct Transcript of GLOMERULOPATIAS PRIMARIAS PROLIFERATIVAS. Ovillo que se origina en la arteriola aferente y drenan en la eferente.

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Supplemental Content Full text links. J Am Soc Nephrol.

World Kidney Day 2016: averting the legacy of kidney disease-focus on childhood.

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Membranoproliferative glomerulonephritis and C3 glomerulopathy: Se proponen dos tipos de GnMP Figura Although there are no specific treatments currently available for C3G, a better understanding of their pathogenesis would set the stage for the possible use glomerklopatias anti-complement drugs, as eculizumab.

Nat Rev Immunol ;9: Clin Nephrol ; See more popular or the latest prezis. Bomback et al, recientemente han publicado una serie de 6 casos 3 con DDD y 3 con GnC3 tratados con eculizumab.

Glomerulopatías C3. Una nueva perspectiva en enfermedades glomerulares

Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies. Los microorganismos que se han vinculado a esta glomerulonefritis incluyen el Estafilococo, Micobacterias, Estreptococo, Propionibacterium acnes, Mycoplasma pneumoniae, Brucella, Coxiella burnetii, Nocardia, Meningococo, Plasmodium y Schistosoma. Composition of nephritic factor generated glomerular deposits in membranoproliferative glomerulonephritis type 2.

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World Kidney Day averting the legacy of kidney disease-focus on childhood. – PubMed – NCBI

Present to your audience Glomerulopatia remote presentation. Sethi S, Fervenza FC. Use of eculizumab for atypical haemolytic uraemic syndrome and C3 glomerulopathies. Membranoproliferative glomerulonephritis type II dense deposit disease: C3 deposition glomerulopathy due to a functional factor H defect.

En una cohorte recientemente publicada, Servais et al.

Glomerulopatias secundarias by Maria Elizabeth Salazar- Maulen on Prezi

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A veces el componente exudativo es tan importante que puede sugerir una Gn postinfecciosa. Send link to edit together this prezi using Prezi Meeting learn more: Send the link below via email or IM. Invited audience members will follow you as you navigate and present People invited to a presentation do not need a Prezi account This link expires 10 minutes after you close the presentation A maximum of 30 users can follow your presentation Learn more about this feature in our knowledge base article.

Do you really want to delete this prezi? Bomback A, Appel GB. El tratamiento en estos casos consiste en la terapia inmunomoduladora eficaz en el control de la enfermedad de base.

The evaluation of C3G in a patient should focus on the complement cascade, as deregulation of the alternative pathway and terminal complement cascade underlies pathogenesis. Eculizumab for dense deposit disease and C3 glomerulonephritis. Manifestaciones Clinicas La proteinuria y la insuficiencia renal son las manifestaciones principales de la amiloidosis renal.

Chronic kidney disease CKD in childhood differs from that in adults, as the largest diagnostic group among children includes congenital anomalies and inherited disorders, with glomerulopathies and kidney disease in the setting of diabetes being relatively uncommon.