ty -jour a2 -saccucci，P.A2 -LópezGinés，C.A2 -Cotter，P.D。Au -Gupta，Neerja au -Kaul -Kaul -Kaul，Anita au -Kabra -Kabra，Madhulika py -2013 da -2013 da -2013/07/29 ti -prenatal诊断of Fetal Peters’ Plus Syndrome: A Case Report SP - 364529 VL - 2013 AB - 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. SN - 2090-6544 UR - https://doi.org/10.1155/2013/364529 DO - 10.1155/2013/364529 JF - Case Reports in Genetics PB - Hindawi Publishing Corporation KW - ER -