Article

Prenatal Diagnosis of Peters-Plus Syndrome: A Case Report

2025-12-11

Abstract excerpt

Peters-Plus syndrome is a rare autosomal recessive disorder characterized by multisystem involvement, with a primary manifestation in the anterior segment of the eye. The hallmark feature, Peters anomaly, presents as central corneal opacity with iridocorneal adhesions. Clinically, patients often exhibit the classic triad of anterior chamber defects, short stature, and brachydactyly, accompanied by craniofacial dys...

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Literature Corpus work: 7fd5cf08-5e0c-5c80-b14f-6c4e11782239
DOI: 10.20944/preprints202512.0997.v1

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