CareLit Fachartikel

Prenatal detection of chromosomal abberations: A case report of Trisomy 9

F Mraihi, A Gharsa, S Schlömann, A Achour, D Chelly · Geburtshilfe und Frauenheilkunde · 2016 · Heft 05

Dokument
1115865
CareLit-ID
Jahr
2016
Publikation
PDF
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Metadaten
DOI
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Bibliografische Angaben

Zeitschrift
Geburtshilfe und Frauenheilkunde
Autor:innen
F Mraihi, A Gharsa, S Schlömann, A Achour, D Chelly
Ausgabe
Heft 05 / 2016
Seiten
–
Erschienen: 2016-05-19 00:00:00
ISSN
0016-5751

Zusammenfassung

Introduction: Trisomy 9 is a rare chromosomal abnormality. It combines multiple defects giving a poor prognosis. The therapeutic pregancy interruption is always an option. Case study: We reported a case of a 35- year -patient who had no pathological history and non-consanguineous marriage. She had two children in good health. During this pregnancy, the first trimester ultrasound and measurement of nuchal translucency were not performed. A cystic hygroma was discovered at 18 WG associated to a complex cardiac defect and a left diaphragmatic hernia, without other Ultrasound signs. Amniocentesis showed Trisomy 9. A…

Schlagworte

Amniocentesis Diagnosis Geburtshilfe und Frauenheilkunde