Underrecognized Frasier syndrome revisited: Paradoxical immunocomplex deposition.

Fujita, Masashi; Aizawa, Tomomi; Tsugawa, Koji; Mattinzoli, Deborah; Nozu, Kandai; Joh, Kensuke; Tanaka, Hiroshi

Fujita, Masashi; Aizawa, Tomomi; Tsugawa, Koji; Mattinzoli, Deborah; Nozu, Kandai; Joh, Kensuke; Tanaka, Hiroshi.

Afiliação

Fujita M; Department of Pediatrics, Hirosaki University Hospital, Hirosaki, Japan.
Aizawa T; Department of Pediatrics, Hirosaki University Hospital, Hirosaki, Japan.
Tsugawa K; Department of Pediatrics, Hirosaki University Hospital, Hirosaki, Japan.
Mattinzoli D; Department of Pediatrics, Renal Research Laboratory, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Nozu K; Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
Joh K; Department of Pathology, The Jikei Medical University, Tokyo, Japan.
Tanaka H; Department of Pediatrics, Hirosaki University Hospital, Hirosaki, Japan.

Pediatr Int ; 64(1): e15350, 2022 01.

Article em En | MEDLINE | ID: mdl-36421979

Assuntos

Glomerulosclerose Segmentar e Focal; Síndrome Nefrótica; Humanos; Síndrome de Frasier

Palavras-chave

Frasier syndrome; Wilms' tumor suppressor gene 1; immunocomplex deposition; membranoproliferative lesion

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Glomerulosclerose Segmentar e Focal / Síndrome Nefrótica Limite: Humans Idioma: En Revista: Pediatr Int Assunto da revista: PEDIATRIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Japão

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