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

• Main Authors: Kyoung Sung Yun (Author), Seung Han Shin (Author), Jaemoon Koh (Author), Jung Min Ko (Author), Jung Yoon Choi (Author), Nam-Joon Yi (Author)
• Format: Book
• Published: Elsevier, 2024-09-01T00:00:00Z.
• Subjects: article
• Online Access: 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...