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[Identification of a novel PAX6 mutation in a sporadic case with congenital aniridia]
Chuan Zhang1, Shengju Hao1, Qinghua Zhang1
1Gansu Provincial Key Laboratory of Birth Defects Prevention and Control, Gansu Provincial Maternal and Child Health Care Hospital, Lanzhou, Gansu 730050, China.
Objective:
To identify mutation of the PAX6 gene in a patient with congenital aniridia.
Methods:
DNA was extracted from peripheral blood sample of the patient and analyzed by direct PCR-Sanger sequencing.
Results:
The proband was found to harbor a heterozygous c.239T>A (p.Ile80Asn) mutation of the PAX6 gene. The same mutation was not found in his parents and 150 healthy controls.
Conclusion:
A novel mutation of the PAX6 gene has been identified in a sporadic case with congenital aniridia.
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