Genetic and pathological findings in a boy with psoriasis and C3 glomerulonephritis: A case report and literature review-Reference-Cited by-同舟云学术

Genetic and pathological findings in a boy with psoriasis and C3 glomerulonephritis: A case report and literature review

Published:2020-07-28 Issue:10 Volume:8 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Wei Lei¹,Fang Ye²³,Cao Guanghai¹,Zhang Shufeng¹,Tian Ming¹,Shen Qian²³,Xu Hong²³,Liu Cuihua¹,Rao Jia²³⁴^ORCID

Affiliation:

1. Department of Nephrology and Rheumatology Children's Hospital of Zhengzhou UniversityHenan Children’s HospitalZhengzhou Children’s Hospital Zhengzhou Henan China

2. Department of Nephrology Children's Hospital of Fudan UniversityNational Pediatric Medical Center of China Shanghai China

3. Shanghai Kidney Development and Pediatric Kidney Disease Research Center Shanghai China

4. Shanghai Key Lab of Birth Defect Children's Hospital of Fudan University Shanghai China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1430

Reference21 articles.

1. The paracaspase MALT 1 mediates CARD 14‐induced signaling in keratinocytes

2. Widening spectrum of renal involvement in psoriasis: First reported case of C3 glomerulonephritis in a psoriatic patient

3. Recent insights into C3 glomerulopathy

4. Observations of a large Dent disease cohort

5. Psoriasis

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