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Case Reports in Genetics
Volume 2013, Article ID 364529, 3 pages
http://dx.doi.org/10.1155/2013/364529
Case Report

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

1Division of Genetics, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi 110029, India
2Fetal Medicine Unit, Indraprastha Apollo Hospital, New Delhi, India

Received 19 June 2013; Accepted 9 July 2013

Academic Editors: P. D. Cotter, C. López Ginés, and P. Saccucci

Copyright © 2013 Neerja Gupta et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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.