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Updated: May 8, 2026

FISH for Pre-implantation Genetic Diagnosis
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Prenatal diagnosis of fetal peters' plus syndrome: a case report
Neerja Gupta1, Anita Kaul, Madhulika Kabra
1Division of Genetics, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi 110029, India.
Abstract:
Peters' plus syndrome is a rare but clinically recognizable autosomal recessive ocular genetic syndrome. Diagnosis during the fetal life is challenging due to the presence of nonspecific findings such as ventriculomegaly in the growth-retarded fetuses. We report the first case of fetal Peters' plus syndrome from India, where fetal ultrasound and the family history were helpful in providing a clue to the diagnosis that was confirmed later on by the DNA analysis.
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