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

Abstract EN

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.