First trimester diagnosis of an unusual case of double aneuploidy with karyotype 48,XXY,+18 (Klinefelter-Edwards syndromes)

Objective: Double aneuploidy cases involving autosomal and sex chromosomes are very rare. Therefore, it is difficult to determine the clinical features and prognosis of these cases. In this case, a fetus with 48,XYY,+18 karyotype is presented. Case(s): Cystic hygroma, cleft lip and palate, and clubb...

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Bibliografski detalji
Glavni autori: Hakan Gölbaşı (Autor), Merve Saka Güvenç (Autor), Ceren Gölbaşı (Autor), İbrahim Ömeroğlu (Autor), Atalay Ekin (Autor)
Format: Knjiga
Izdano: Perinatal Medicine Foundation, 2022-04-01T00:00:00Z.
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