Nefropatía por IGA

Se realizó una revisión bibliográfica. La bibliografía correspondiente a los últimos años se consultó con el objetivo de profundizar en el estudio de la nefropatía IgA y se revisaron las características patogénicas y clinicopatogénicas de la enfermedad, así como su abordaje terapéutico. La nefropatí...

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Published in:Revista cubana de pediatria Vol. 72; no. 3; pp. 194 - 202
Main Authors: González García, Oria, Álvarez Díaz, Saylí, Morell Contreras, Mercedes, Espinosa López, Digna Ma
Format: Journal Article
Language:Portuguese
Spanish
Published: Editorial Ciencias Médicas 01-09-2000
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Abstract Se realizó una revisión bibliográfica. La bibliografía correspondiente a los últimos años se consultó con el objetivo de profundizar en el estudio de la nefropatía IgA y se revisaron las características patogénicas y clinicopatogénicas de la enfermedad, así como su abordaje terapéutico. La nefropatía IgA se reconoce como la causa más común de enfermedad glomerular y fueron la hematuria recurrente y la presencia de depósitos de IgA en el mesangio, los signos clínicos y patológicos más característicos de esta enfermedad. La nefropatía IgA no es una afección benigna, su evolución es crónica y progresiva. La proteinuria es un indicador de mal pronóstico y no existe un tratamiento específico eficaz para ella por lo que constituye un reto para el futuro.
AbstractList Se realizó una revisión bibliográfica. La bibliografía correspondiente a los últimos años se consultó con el objetivo de profundizar en el estudio de la nefropatía IgA y se revisaron las características patogénicas y clinicopatogénicas de la enfermedad, así como su abordaje terapéutico. La nefropatía IgA se reconoce como la causa más común de enfermedad glomerular y fueron la hematuria recurrente y la presencia de depósitos de IgA en el mesangio, los signos clínicos y patológicos más característicos de esta enfermedad. La nefropatía IgA no es una afección benigna, su evolución es crónica y progresiva. La proteinuria es un indicador de mal pronóstico y no existe un tratamiento específico eficaz para ella por lo que constituye un reto para el futuro.
Author Espinosa López, Digna Ma
Álvarez Díaz, Saylí
González García, Oria
Morell Contreras, Mercedes
AuthorAffiliation Hospital Pediátrico Universitario Centro Habana
Hospital Pediátrico William Soler
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  givenname: Oria
  surname: González García
  fullname: González García, Oria
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  givenname: Saylí
  surname: Álvarez Díaz
  fullname: Álvarez Díaz, Saylí
  organization: Hospital Pediátrico William Soler
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  givenname: Mercedes
  surname: Morell Contreras
  fullname: Morell Contreras, Mercedes
  organization: Hospital Pediátrico Universitario Centro Habana
– sequence: 4
  givenname: Digna Ma
  surname: Espinosa López
  fullname: Espinosa López, Digna Ma
  organization: Hospital Pediátrico Universitario Centro Habana
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Keywords GLOMERU-LONEPHRITIS, IGA
GLOMERULONEFRITIS
GLOMERULONEPHRITIS, IGA
CHILD
NIÑO
GLOMERULONEFRITIS POR IGA
Language Portuguese
Spanish
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