Full-house nephropathy associated with high expression of SPATA5L1 due to a genetic pathogenic variant
Rheumatology (Oxford)
.
2022 Apr 11;61(4):e84-e86.
doi: 10.1093/rheumatology/keab896.
Authors
Luciana Martins de Carvalho
1
2
,
Graziella Ribeiro de Sousa
3
,
Ronald Moura
4
,
Fabiano Saggioro
5
6
,
Inalda Facincani
1
,
Roberto Costa
7
,
Paola Pinheiro Kahwage
1
2
,
Rosane Gomes de Paula Queiroz
1
,
Elvis Terci Valera
1
,
Sergio Crovella
8
,
Paula Sandrin-Garcia
9
10
Affiliations
1
Department of Pediatrics.
2
Division of Pediatric Rheumatology.
3
Department of Genetics, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto, Brazil.
4
Department of Advanced Diagnostics, Institute for Maternal and Child Health-IRCCS "Burlo Garofolo", Trieste, Italy.
5
Department of Pathology, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto.
6
Department of Pathology, Rede D'Or, São Paulo, SP.
7
Department of Medicine, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto, Brazil.
8
Department of Biological and Environmental Sciences, College of Arts and Sciences, Qatar University, Doha, Qatar.
9
Keizo Asami Immunopathology Laboratory.
10
Genetics Department, Federal University of Pernambuco, Recife, Brazil.
PMID:
34864870
DOI:
10.1093/rheumatology/keab896
No abstract available
Publication types
Research Support, Non-U.S. Gov't
MeSH terms
Humans
Kidney Diseases*
Lupus Nephritis* / pathology