prenatal diagnosis of fetal peters’ plus syndrome: a case report
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ID: 164764
2013
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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.
| Reference Key |
gupta2013caseprenatal
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|---|---|
| Authors | ;Neerja Gupta;Anita Kaul;Madhulika Kabra |
| Journal | journal of food processing and preservation |
| Year | 2013 |
| DOI |
10.1155/2013/364529
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| URL | |
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