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Updated: Apr 29, 2026

Determining the Likelihood of Variant Pathogenicity Using Amino Acid-level Signal-to-Noise Analysis of Genetic Variation
Published on: January 16, 2019
An unusual presentation of Kabuki syndrome: clinical overlap with CHARGE syndrome
Judith M A Verhagen1, Wilma Oostdijk2, Cecilia E J Terwisscha van Scheltinga3
1Department of Clinical Genetics, Erasmus Medical Center Rotterdam, The Netherlands.
Abstract:
Kabuki syndrome is a rare genetic disorder characterized by intellectual disability and multiple congenital anomalies, including short stature, peculiar facial appearance, skeletal anomalies, a variety of visceral malformations and abnormal dermatoglyphic patterns. We describe a case of Kabuki syndrome presenting with atypical features, consisting of bilateral microphthalmia, coloboma, anal atresia and panhypopituitarism, showing considerable phenotypic overlap with CHARGE syndrome. This report demonstrates that clinical follow-up and molecular genetic testing can be useful for establishing the correct diagnosis.
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