A case report of a preterm infant with KBG syndrome and hepatoblastoma

• Glavni autori: Kyoung Sung Yun (Autor), Seung Han Shin (Autor), Jaemoon Koh (Autor), Jung Min Ko (Autor), Jung Yoon Choi (Autor), Nam-Joon Yi (Autor)
• Format: Knjiga
• Izdano: Elsevier, 2024-09-01T00:00:00Z.
• Teme: article
• Online pristup: Connect to this object online.

Background: KBG syndrome is a rare autosomal dominant genetic disease characterized by facial dysmorphism, developmental disorders, and short stature. The syndrome is caused by the haploinsufficiency of the ankyrin repeat domain-containing protein 11 (ANKRD11). Recently, there have been concerns tha...