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.
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.
Area of Science:
- Genetics
- Pediatrics
- Medical Imaging
Background:
- Ciliopathies are a group of genetic disorders caused by defects in cilia.
- NPHP3 gene mutations are a known cause of nephronophthisis, a type of ciliopathy.
- Fetal hyper-echogenic kidneys can be an ultrasound finding suggestive of certain genetic conditions.
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