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Possibilities and Limitations of Prenatal Diagnosis of Rare Imprinting Syndromes: Prader–Willi Syndrome

2025-12-16

Abstract excerpt

<h4>Background: </h4> Prader-Willi syndrome (PWS) is a multisystemic complex imprinting disorder. Prenatal diagnosis of PWS is still a challenge with non-specific ultrasound markers and limitations for diagnosis with non-invasive screening methods. Prenatal suspicion and early postnatal diagnosis are mandatory for promoting healthy growth and development, preventing complications, and providing health care profess...

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Literature Corpus work
3e4a9556-4310-56c8-8159-0f1d5f4c68a8
DOI
10.20944/preprints202512.1379.v1
Open publication

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Possibilities and Limitations of Prenatal Diagnosis of Rare Imprinting Syndromes: Prader–Willi SyndromeDOI 10.20944/preprints202512.1379.v1
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