A case of congenital nephrotic syndrome with crescents caused by a novel compound heterozygous pairing of NPHS1 genetic variants

Authors

Kyle N Goodman, Washington University School of Medicine in St. Louis
Pongpratch Puapatanakul, Washington University School of Medicine in St. Louis
Kevin T Barton, Washington University School of Medicine in St. Louis
Mai He, Washington University School of Medicine in St. Louis
Jeffrey H Miner, Washington University School of Medicine in St. Louis
Joseph P Gaut, Washington University School of Medicine in St. Louis

Journal

Case Reports in Nephrology

Publication Date

2-27-2024

Volume

2024

First Page

5121375

Document Type

Open Access Publication

DOI

10.1155/2024/5121375

Rights and Permissions

Goodman KN, Puapatanakul P, Barton KT, He M, Miner JH, Gaut JP. A Case of Congenital Nephrotic Syndrome with Crescents Caused by a Novel Compound Heterozygous Pairing of NPHS1 Genetic Variants. Case Rep Nephrol. 2024 Feb 27;2024:5121375. doi: 10.1155/2024/5121375. Copyright © 2024 Kyle N. Goodman et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Recommended Citation

Goodman, Kyle N; Puapatanakul, Pongpratch; Barton, Kevin T; He, Mai; Miner, Jeffrey H; and Gaut, Joseph P, "A case of congenital nephrotic syndrome with crescents caused by a novel compound heterozygous pairing of NPHS1 genetic variants." Case Reports in Nephrology. 2024, 5121375 (2024).
https://digitalcommons.wustl.edu/oa_4/3581

Department

ICTS (Institute of Clinical and Translational Sciences)