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Hindawi, Case Reports in Genetics, (2013), p. 1-3, 2013

DOI: 10.1155/2013/364529

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Prenatal Diagnosis of Fetal Peters' Plus Syndrome: A Case Report

Journal article published in 2013 by Neerja Gupta ORCID, Anita Kaul, Madhulika Kabra
This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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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.