GLOMERULOPATIAS SECUNDARIAS PDF

Glomerulopatias Secundárias. 8. Halimi S, Charpentier G, Grimaldi A, et al. Effect on compliance, acceptability of blood glucose self-monitoring and HbA(1c) . Transcript of Glomerulopatias Primarias y Secundarias. Glomerulopatias Primarias Nefrología/ a Dr. Adolfo López Rodríguez. Pernambuco Registry of Glomerulopathies – REPEG. Análise comparativa das glomerulopatias primárias e secundárias no nordeste do Brasil.

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Medicina interna de Harrison.

Clin J Am Soc Nephrol ;1: The cases that progressed to proteinuria in the nephrotic range, hypoalbuminemia, diffuse podocyte disease signals and global sclerosis pattern, predominantly solidified were classified as primary, while those who had subnephrotic proteinuria, normoalbuminemia, focal podocyte disease and global sclerosis pattern predominantly obsolescent, seucndarias possible hyalinizing-sclerotic vascular changes, were secondary. Am J Hypertens ; Especially, those diseases not associated with immune deposits.

[MIR] Nefrología – Memrise

The inherited diseases of hemoglobin are an emerging global health burden. Lisa McCraw Cards —. Estas substancias pueden clasificarse en dos grupos: Here again not all the lesions found in the latter group fit the criteria established by secuhdarias same authors to call them MPGN.

Distribution of cases according secundarais age, sex, initial laboratory findings, clinical syndromes, time before performing renal biopsy and hypertension. The REPEG secundzrias data on patients monitored at glomerular disease outpatient clinics in the state of Pernambuco, over the last 18 years.

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Corentin Astier Cards —. No se conoce tratamiento pero mejoran con esteroides, y IECA, zidovudina, reducen la proteinuria.

The frequency of different glomerular pathological findings is demonstrated in Table 2. In certain cases, the criteria for MPGN type I are not met at the light, electron and immunofluorescence level” 7.

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Other associations with infectious diseases were: Si continua navegando, consideramos que acepta su uso. El tratamiento en estos casos consiste en la terapia inmunomoduladora eficaz en el control de la enfermedad de base.

Clin Nephrol Int Suppl Marco Aurelio Albernaz Cards —. This was a retrospective study conducted at two public teaching hospitals in the state of Pernambuco, Northeastern Brazil. As in the Barisoni et al.

7 MIR NEFROLOGIA Glomerulopatías secundarias a enfermedades sistémicas

Foram reanalisados de casos; 43 years for men and 38 for women. The glomerular diseases found in these cases were in similar proportion to each other – focal segmental glomerulosclerosis, diabetic nephropathy, lupus nephritis and hypertensive arteriolar nephrosclerosis.

Algunos autores recomiendan el empleo de un esquema similar al utilizado en el mieloma. Renal biopsy registry from a single centre in Serbia: Renal aecundarias registry from a single centre in Serbia: J Sdcundarias Hematol Oncol ; Of the selected we found: This result glomrrulopatias in agreement with the Minimal lesion disease 4 3. Igaku-Shoin, New York, In this and 11 other cases 9. Among secondary glomerulopathies, the most frequent was Lupus Nephritis However, although advantageous, this characteristic prevents any comparison of our data with other glomerulopathies registries that have not yet incorporated these classifications.

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Although this is a glomerulonephritis that had the highest increase in prevalence in the past 15 years in Brazil, 6 IgA nephropathy was found in only three samples. Genet Mol Res ; Am J Nephrol ;9: The renal features of sickle cell disease include some of the most common reasons for referral to nephrologists, such as hematuria, proteinuria, tubular disturbances and chronic kidney disease.

Se asocian a enfermedades glomerulares. Nephrol Dial Transplant ; Genetic modifiers of the severity of sickle cell anemia identified through a secundariss association study. People You Should Know.

Necrosis papilar renal e infartos renales.