An unusual kidney presentation of severe proteinuria in a 2-year-old girl: Answers.

Nawata, Aya; Morishita, Takahiro; Hisano, Satoshi; Nakagawa, Kaneyasu; Kusuhara, Koichi; Nakayama, Toshiyuki

Nawata, Aya; Morishita, Takahiro; Hisano, Satoshi; Nakagawa, Kaneyasu; Kusuhara, Koichi; Nakayama, Toshiyuki.

Afiliação

Nawata A; Department of Pathology, School of Medicine, University of Occupational and Environmental Health, 1-1 Iseigaoka, Yahatanishi-ku, Kitakyushu, Fukuoka, Japan. aya.y0116@gmail.com.
Morishita T; Department of Pediatrics, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, Japan.
Hisano S; Department of Pathology, School of Medicine, University of Occupational and Environmental Health, 1-1 Iseigaoka, Yahatanishi-ku, Kitakyushu, Fukuoka, Japan.
Nakagawa K; Department of Medicine and Clinical Science, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Kusuhara K; Department of Pediatrics, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, Japan.
Nakayama T; Department of Pathology, School of Medicine, University of Occupational and Environmental Health, 1-1 Iseigaoka, Yahatanishi-ku, Kitakyushu, Fukuoka, Japan.

Pediatr Nephrol ; 36(5): 1153-1157, 2021 05.

Article em En | MEDLINE | ID: mdl-32789578

Palavras-chave

Child; Epilepsy; Facial dysmorphism; Galloway-Mowat syndrome; Glomerular endothelial cell injury; Kidney-limited thrombotic microangiopathy; Severe proteinuria

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Pediatr Nephrol Assunto da revista: NEFROLOGIA / PEDIATRIA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Japão

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