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

• Hoofdauteurs: Kyoung Sung Yun (Auteur), Seung Han Shin (Auteur), Jaemoon Koh (Auteur), Jung Min Ko (Auteur), Jung Yoon Choi (Auteur), Nam-Joon Yi (Auteur)
• Formaat: Boek
• Gepubliceerd in: Elsevier, 2024-09-01T00:00:00Z.
• Onderwerpen: article
• Online toegang: 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...