Jacobsen syndrome: a case report and clinical features of a rare genetic syndrome

• Váldodahkkit: Kazım Öztarhan (Dahkki), Talya Kaptaç (Dahkki), Mutlu Karkucak (Dahkki), Ece Öztarhan (Dahkki), Ali Gedikbaşı (Dahkki)
• Materiálatiipa: Girji
• Almmustuhtton: Perinatal Medicine Foundation, 2022-12-01T00:00:00Z.
• Fáttát: article
• Liŋkkat: Connect to this object online.

Objective: Jacobsen syndrome is an infrequent contiguous gene syndrome that involves the deletion of the long arm of chromosome 11. It is mostly accompanied by intellectual disability and other abnormalities. The majority of the patients are hospitalized or lost within the first two years of life. C...