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

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&#...

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Detalles Bibliográficos
Autores principales:	Gupta, Neerja, Kaul, Anita, Kabra, Madhulika
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Hindawi Publishing Corporation 2013
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3745879/ https://www.ncbi.nlm.nih.gov/pubmed/23984120 http://dx.doi.org/10.1155/2013/364529

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