Case Report: Unusual Aggregation of Different Glomerulopathies in a Family Resolved by Genetic Testing and Reverse Phenotyping.

Kumar, Reeti; Keskinyan, Vahakn; Stangl, Megan Chryst; Lane, Brandon M; Buckley, Anne F; Barisoni, Laura; Howell, David N; Gbadegesin, Rasheed A

Kumar, Reeti; Keskinyan, Vahakn; Stangl, Megan Chryst; Lane, Brandon M; Buckley, Anne F; Barisoni, Laura; Howell, David N; Gbadegesin, Rasheed A.

Afiliação

Kumar R; Division of Nephrology, Department of Pediatrics, Duke University Medical Center, Durham, NC, United States.
Keskinyan V; Division of Nephrology, Department of Pediatrics, Duke University Medical Center, Durham, NC, United States.
Stangl MC; Division of Nephrology, Department of Pediatrics, Duke University Medical Center, Durham, NC, United States.
Lane BM; Division of Nephrology, Department of Pediatrics, Duke University Medical Center, Durham, NC, United States.
Buckley AF; Division of Renal Pathology, Department of Pathology, Duke University Medical Center, Durham, NC, United States.
Barisoni L; Division of Renal Pathology, Department of Pathology, Duke University Medical Center, Durham, NC, United States.
Howell DN; Division of Renal Pathology, Department of Pathology, Duke University Medical Center, Durham, NC, United States.
Gbadegesin RA; Division of Nephrology, Department of Pediatrics, Duke University Medical Center, Durham, NC, United States.

Front Pediatr ; 10: 826330, 2022.

Article em En | MEDLINE | ID: mdl-35295700

Palavras-chave

COL4A5 gene; IgA nephropathy; acute glomerulonephritis; glomerular disease; reverse phenotype

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Front Pediatr Ano de publicação: 2022 Tipo de documento: Article

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