A Rare Cause of Hyperinsulinemic Hypoglycemia: Kabuki Syndrome
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...
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Autores principales: | Mina Mısırlıgil, Yılmaz Yıldız, Onur Akın, Sevinç Odabaşı Güneş, Mutluay Arslan, Bülent Ünay |
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Formato: | article |
Lenguaje: | EN |
Publicado: |
Galenos Yayincilik
2021
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Materias: | |
Acceso en línea: | https://doaj.org/article/027c57406003485e89453a93e2924fd3 |
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