A Rare Cause of Hyperinsulinemic Hypoglycemia: Kabuki Syndrome

• Main Authors: Mina Mısırlıgil (Author), Yılmaz Yıldız (Author), Onur Akın (Author), Sevinç Odabaşı Güneş (Author), Mutluay Arslan (Author), Bülent Ünay (Author)
• Format: Book
• Published: Galenos Yayincilik, 2021-12-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Kabuki syndrome (KS) is a disease characterized by distinctive facial features, skeletal anomalies and delay in neuromotor development. KS 1 is an autosomal dominant condition caused by mutations in the KMT2D gene, whereas KS 2 is an X-linked disorder caused by mutations in the KDM6A gene. In the ma...