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J. Bras. Nefrol. vol.38 número2

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E

RRATA

|

E

RRATUM

271

E

VITANDOOLEGADODADOENÇARENAL

- F

OCONAINFÂNCIA

A

VERTINGTHELEGACYOFKIDNEYDISEASE

-

FOCUSONCHILDHOOD

Julie R Ingelfinger 1,2, Franz Schaefer 3, Kamyar Kalantar-Zadeh 4,5em nome da World Kidney Day

Steering Committee*

1 Harvard Medical School. 2 Massachusetts General Hospital. 3 University of Heidelberg Head. 4 University of California Irvine. 5 UCLA Fielding School of Public Health.

*Os membros do Comité Administrativo do Dia Mundial do Rim são: Philip Kam Tao Li, Guillermo Garcia-Garcia, William G. Couser, Timur Erk, Julie R Ingelfinger, Kamyar Kalantar-Zadeh, Charles Kernahan, Charlotte Osafo, Miguel C. Riella, Luca Segantini, Elena Zakharova.

No Editorial publicado no Jornal Brasileiro de Nefrologia 38 (1), com número de DOI:

10.5935/0101-2800.20160002, na Tabela 2 onde se lê "HA: Hipertensão Arterial" leia-se

NH: Nefropatia hereditária.

Volume 38 Edição 1 - Jan/Fev/Mar 2016

DOI: 10.5935/0101-2800.20160039

DRC

DRT

Etiologia

Porcentagem

(Faixa)

Etiologia

Percontagem

(Faixa)

CAKUT

48-59%

CAKUT

34-43%

GN

5-14%

GN

15-29%

NH

10-19%

HA

12-22%

SHU

2-6%

SHU

2-6%

Cística

5-9%

Cística

6-12%

Isquêmica

2-4%

Isquêmica

2%

Causas raras incluem SN congênita, doenças metabólicas, cistinose/ Causas mistas dependem de como tais entidades são classificadas CAKUT: Anomalias congênitas do rim e trato urinário; GN: Glomerulonefrite; NH: Nefropatia hereditária; SHU: Síndrome Hemolítica-Urêmica *de Harambat

et al. Dados da DRC do NAPRTCS, Dados Italianos e Dados Belgas. Dados sobre a DRT vêm de ANZDATA, ESPN/ERA-EDTA, UK Renal Registry e do Registro Japonês.

Referências

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