Homozygous mutation in the NPHP3 gene causing foetal nephronophthisis

Uzma Abdullah1, Muhammad Farooq2,3, Ambrin Fatima1

  • 1Human Molecular Genetics Laboratory, Health Biotechnology Division, National Institute for Biotechnology and Genetic Engineering (NIBGE), PIEAS, Faisalabad, Pakistan.

Nephrology (Carlton, Vic.)
|September 19, 2017
PubMed
Summary

This study identified a rare NPHP3 gene mutation in a Pakistani family presenting with fetal hyper-echogenic kidneys. Molecular testing is crucial for diagnosing ciliopathies and assessing familial risks.

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