Distinctively Different Phenotypes of Two Cases with a Rare Karyotype of 45,X/47,XYY Mosaicism: Case Report and Literature Review

• Ngā kaituhi matua: Özge Köprülü (Author), Sezer Acar (Author), Kadri Murat Erdoğan (Author), Özlem Nalbantoğlu (Author), Tarık Kırkgöz (Author), Gülçin Arslan (Author), Beyhan Özkaya (Author), Yaşar Bekir Kutbay (Author), Behzat Özkan (Author)
• Hōputu: Pukapuka
• I whakaputaina: Galenos Yayinevi, 2022-12-01T00:00:00Z.
• Ngā marau: article
• Urunga tuihono: Connect to this object online.

The 45,X/47,XYY mosaicism is an extremely rare genetic disorder with highly phenotypic manifestations such as ovotesticular disorders of sexual development, mixed gonadal dysgenesis and Turner syndrome. Herein, we report two cases with very distinctive phenotypes despite having the same sex chromoso...