APOL1-Associated Collapsing Focal Segmental Glomerulosclerosis in a Patient With Stimulator of Interferon Genes (STING)-Associated Vasculopathy With Onset in Infancy (SAVI).

Abid, Qassim; Best Rocha, Alejandro; Larsen, Christopher P; Schulert, Grant; Marsh, Rebecca; Yasin, Shima; Patty-Resk, Cathy; Valentini, Rudolph P; Adams, Matthew; Baracco, Rossana

Abid, Qassim; Best Rocha, Alejandro; Larsen, Christopher P; Schulert, Grant; Marsh, Rebecca; Yasin, Shima; Patty-Resk, Cathy; Valentini, Rudolph P; Adams, Matthew; Baracco, Rossana.

Afiliação

Abid Q; Division of Pediatric Nephrology, Department of Pediatrics, Wayne State University, Children's Hospital of Michigan, Detroit, MI.
Best Rocha A; Arkana Laboratories, Little Rock, AR.
Larsen CP; Division of Pediatric Nephrology, Department of Pediatrics, Wayne State University, Children's Hospital of Michigan, Detroit, MI.
Schulert G; Division of Rheumatology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH.
Marsh R; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH; Division of Bone Marrow Transplantation & Immune Deficiency, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Yasin S; Division of Rheumatology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Patty-Resk C; Division of Pediatric Rheumatology, Department of Pediatrics, Wayne State University, Children's Hospital of Michigan, Detroit, MI.
Valentini RP; Division of Pediatric Nephrology, Department of Pediatrics, Wayne State University, Children's Hospital of Michigan, Detroit, MI.
Adams M; Division of Pediatric Rheumatology, Department of Pediatrics, Wayne State University, Children's Hospital of Michigan, Detroit, MI.
Baracco R; Division of Pediatric Nephrology, Department of Pediatrics, Wayne State University, Children's Hospital of Michigan, Detroit, MI. Electronic address: rbaracco@med.wayne.edu.

Am J Kidney Dis ; 75(2): 287-290, 2020 02.

Article em En | MEDLINE | ID: mdl-31601430

Assuntos

Apolipoproteína L1/genética; DNA/genética; Glomerulosclerose Segmentar e Focal/genética; Interferon Tipo I/metabolismo; Doenças Vasculares/etiologia; Apolipoproteína L1/metabolismo; Genótipo; Glomerulosclerose Segmentar e Focal/metabolismo; Glomerulosclerose Segmentar e Focal/patologia; Humanos; Recém-Nascido; Glomérulos Renais/ultraestrutura; Masculino; Microscopia Eletrônica; Doenças Vasculares/diagnóstico; Doenças Vasculares/metabolismo

Palavras-chave

African ancestry; Apolipoprotein L1 (APOL1); SAVI; case report; collapsing glomerulopathy; focal segmental glomerulosclerosis (FSGS); genetic risk; inflammatory state; interferon (IFN); interferonopathy; kidney biopsy; kidney disease; risk allele

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Vasculares / DNA / Glomerulosclerose Segmentar e Focal / Interferon Tipo I / Apolipoproteína L1 Tipo de estudo: Diagnostic_studies / Risk_factors_studies Limite: Humans / Male / Newborn Idioma: En Revista: Am J Kidney Dis Ano de publicação: 2020 Tipo de documento: Article País de publicação: Estados Unidos

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