A novel NPHS1 mutation associated with temporary elevation of maternal serum alfa-fetoprotein and late onset of proteinuria

Int Urol Nephrol. 2021 Feb;53(2):391-392. doi: 10.1007/s11255-020-02645-1. Epub 2020 Sep 17.

Authors

Gizem Yıldız¹, Meral Torun Bayram¹, Alper Soylu², Salih Kavukçu³

Affiliations

¹ Department of Pediatric Nephrology, Dokuz Eylül University Medical Faculty, Balçova, 35340, Izmir, Turkey.
² Department of Pediatric Nephrology and Rheumatology, Dokuz Eylül University Medical Faculty, Izmir, Turkey. alper.soylu@deu.edu.tr.
³ Department of Pediatric Nephrology and Rheumatology, Dokuz Eylül University Medical Faculty, Izmir, Turkey.

PMID: 32944892
DOI: 10.1007/s11255-020-02645-1

No abstract available

Publication types

Case Reports
Letter

MeSH terms

Age of Onset
Child
Female
Glomerulosclerosis, Focal Segmental / genetics*
Humans
Membrane Proteins / genetics*
Mutation*
Pregnancy
Proteinuria / genetics*
Time Factors
alpha-Fetoproteins / analysis*

Substances

Membrane Proteins
alpha-Fetoproteins
nephrin