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Updated: Jan 25, 2026

FISH for Pre-implantation Genetic Diagnosis
Published on: February 23, 2011
[Genetic analysis and prenatal diagnosis for a pedigree affected with X-linked Norrie disease]
Xinmiao Yang1, Wenwen Li, Xueping Shen
1Huzhou Maternity and Child Health Care Hospital, Zhejiang 313000, China.
Objective:
To detect mutation of NDP gene in a pedigree affected with Norrie disease.
Methods:
Sanger sequencing was used to analyze the NDP gene at Xp11.3. Prenatal diagnosis was performed on amniotic fluid sample after the causative gene was detected.
Results:
Sanger sequencing has revealed a c.2T>C (p.M1T) missense mutation of the NDP gene in the proband and the fetus. The same variation was not found in ClinVar and HGMD database.
Conclusion:
The c.2T>C mutation of the NDP gene probably underlies the Norrie disease in this pedigree.
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