Article

Prenatal diagnosis of Pfeiffer syndrome type 2 with increased nuchal translucency

2021-04-27

Abstract excerpt

Pfeiffer syndrome (PS) is a rare autosomal dominant genetic disorder characterized by craniosynostosis, broad thumbs / toes. Here we report a case of PS type 2 with increased nuchal translucency at early trimester.

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Literature Corpus work: 49db46d1-5b76-5ee1-aba5-d7cc3a6ffdc3
DOI: 10.22541/au.161953506.64936732/v1

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