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                  <mods:namePart>Narbona-Arias, Isidoro</mods:namePart>
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                  <mods:namePart>Andérica-Herrero, José Ramón</mods:namePart>
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                  <mods:namePart>Gómez-Muñoz, Cristina</mods:namePart>
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                  <mods:namePart>Blasco-Alonso, Marta</mods:namePart>
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                  <mods:namePart>Jiménez-López, Jesús Salvador</mods:namePart>
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               <mods:identifier type="citation">Fortún Agud M, Monís Rodríguez S, Narbona Arias I, Andérica Herrero JR, Gómez Muñoz C, Blasco Alonso M, Jiménez López JS. Prenatal Diagnosis of Peters-Plus Syndrome: A Case Report. Life. 2026; 16(1):92. https://doi.org/10.3390/life16010092</mods:identifier>
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               <mods:identifier type="doi">10.3390/life16010092</mods:identifier>
               <mods:abstract>Peters-Plus syndrome is a rare autosomal recessive disorder caused by biallelic pathogenic
variants in the B3GLCT gene and characterized by multisystem involvement. Fewer than
100 cases have been reported to date, and only a limited number have been diagnosed
prenatally. Prenatal identification is challenging due to the variable and non-specific nature
of fetal findings and the frequent absence of detectable ocular anomalies during routine
ultrasound. We report a prenatal diagnosis of Peters-Plus syndrome in a monochorionic diamniotic
twin pregnancy, based on the progressive identification of early-onset intrauterine
growth restriction, rhizomelic limb shortening, craniofacial dysmorphism, and mild central
nervous system abnormalities. Standard cytogenetic and chromosomal microarray analyses
were normal, prompting extended genetic testing. Prenatal exome sequencing identified
a homozygous pathogenic splice-site variant (c.660+1G>A) in B3GLCT in both fetuses,
confirming the diagnosis. This case highlights the importance of recognizing suggestive
multisystem prenatal findings and the crucial role of advanced genetic testing in achieving
an accurate prenatal diagnosis. Early molecular confirmation enables appropriate parental
counseling regarding prognosis, recurrence risk, and future reproductive options.</mods:abstract>
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                  <mods:topic>Diagnóstico prenatal</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Obstetricia</mods:topic>
               </mods:subject>
               <mods:titleInfo>
                  <mods:title>Prenatal Diagnosis of Peters-Plus Syndrome: A Case Report</mods:title>
               </mods:titleInfo>
               <mods:genre>journal article</mods:genre>
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