Author(s): Lederer D, Grisart B, Digilio MC, Benoit V, Crespin M,
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Abstract Kabuki syndrome (KS) is a rare genetic disease that causes developmental delay and congenital anomalies. Since the identification of MLL2 mutations as the primary cause of KS, such mutations have been identified in 56\%-76\% of affected individuals, suggesting that there may be additional genes associated with KS. Here, we describe three KS individuals with de novo partial or complete deletions of an X chromosome gene, KDM6A, that encodes a histone demethylase that interacts with MLL2. Although KDM6A escapes X inactivation, we found a skewed X inactivation pattern, in which the deleted X chromosome was inactivated in the majority of the cells. This study identifies KDM6A mutations as another cause of KS and highlights the growing role of histone methylases and histone demethylases in multiple-congenital-anomaly and intellectual-disability syndromes. Copyright © 2012 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved.
This article was published in Am J Hum Genet
and referenced in Journal of Steroids & Hormonal Science