Literature DB >> 24862881

An unusual presentation of Kabuki syndrome: clinical overlap with CHARGE syndrome.

Judith M A Verhagen1, Wilma Oostdijk2, Cecilia E J Terwisscha van Scheltinga3, Nicoline E Schalij-Delfos4, Yolande van Bever5.   

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.
Copyright © 2014 Elsevier Masson SAS. All rights reserved.

Entities:  

Keywords:  Anal atresia; Coloboma; Kabuki syndrome; Microphthalmia; Panhypopituitarism

Mesh:

Year:  2014        PMID: 24862881     DOI: 10.1016/j.ejmg.2014.05.005

Source DB:  PubMed          Journal:  Eur J Med Genet        ISSN: 1769-7212            Impact factor:   2.708


  13 in total

1.  UTX-guided neural crest function underlies craniofacial features of Kabuki syndrome.

Authors:  Karl B Shpargel; Joshua Starmer; Chaochen Wang; Kai Ge; Terry Magnuson
Journal:  Proc Natl Acad Sci U S A       Date:  2017-10-09       Impact factor: 11.205

2.  Phenotypic expansion of KMT2D-related disorder: Beyond Kabuki syndrome.

Authors:  Dustin Baldridge; Rebecca C Spillmann; Daniel J Wegner; Jennifer A Wambach; Frances V White; Kathleen Sisco; Tomi L Toler; Patricia I Dickson; F Sessions Cole; Vandana Shashi; Dorothy K Grange
Journal:  Am J Med Genet A       Date:  2020-02-21       Impact factor: 2.802

3.  The KMT2D Kabuki syndrome histone methylase controls neural crest cell differentiation and facial morphology.

Authors:  Karl B Shpargel; Cassidy L Mangini; Guojia Xie; Kai Ge; Terry Magnuson
Journal:  Development       Date:  2020-07-17       Impact factor: 6.862

4.  Rare ocular features in a case of Kabuki syndrome (Niikawa-Kuroki syndrome).

Authors:  Yi-Hsing Chen; Ming-Hui Sun; Shao-Hsuan Hsia; Chi-Chun Lai; Wei-Chi Wu
Journal:  BMC Ophthalmol       Date:  2014-11-24       Impact factor: 2.209

5.  Individual Clinically Diagnosed with CHARGE Syndrome but with a Mutation in KMT2D, a Gene Associated with Kabuki Syndrome: A Case Report.

Authors:  Sonoko Sakata; Satoshi Okada; Kohei Aoyama; Keiichi Hara; Chihiro Tani; Reiko Kagawa; Akari Utsunomiya-Nakamura; Shinichiro Miyagawa; Tsutomu Ogata; Haruo Mizuno; Masao Kobayashi
Journal:  Front Genet       Date:  2017-12-11       Impact factor: 4.599

6.  CHARGE and Kabuki Syndromes: Gene-Specific DNA Methylation Signatures Identify Epigenetic Mechanisms Linking These Clinically Overlapping Conditions.

Authors:  Darci T Butcher; Cheryl Cytrynbaum; Andrei L Turinsky; Michelle T Siu; Michal Inbar-Feigenberg; Roberto Mendoza-Londono; David Chitayat; Susan Walker; Jerry Machado; Oana Caluseriu; Lucie Dupuis; Daria Grafodatskaya; William Reardon; Brigitte Gilbert-Dussardier; Alain Verloes; Frederic Bilan; Jeff M Milunsky; Raveen Basran; Blake Papsin; Tracy L Stockley; Stephen W Scherer; Sanaa Choufani; Michael Brudno; Rosanna Weksberg
Journal:  Am J Hum Genet       Date:  2017-05-04       Impact factor: 11.025

7.  Genetic analysis of CHARGE syndrome identifies overlapping molecular biology.

Authors:  Amanda Moccia; Anshika Srivastava; Jennifer M Skidmore; John A Bernat; Marsha Wheeler; Jessica X Chong; Deborah Nickerson; Michael Bamshad; Margaret A Hefner; Donna M Martin; Stephanie L Bielas
Journal:  Genet Med       Date:  2018-01-04       Impact factor: 8.822

8.  An analysis of body proportions in children with CHARGE syndrome using photogrammetric anthropometry.

Authors:  Bas Penders; Dieuwerke R Dijk; Gianni Bocca; Luc J I Zimmermann; Conny M A van Ravenswaaij-Arts; Willem-Jan M Gerver
Journal:  Am J Med Genet A       Date:  2019-05-27       Impact factor: 2.802

9.  Neuroimaging in Kabuki syndrome and another KMT2D-related disorder.

Authors:  Rachel T Stadelmaier; Margaret A Kenna; Devon Barrett; Thomas E Mullen; Olaf Bodamer; Pankaj B Agrawal; Caroline D Robson; Monica H Wojcik
Journal:  Am J Med Genet A       Date:  2021-08-09       Impact factor: 2.802

10.  A novel KMT2D mutation resulting in Kabuki syndrome: A case report.

Authors:  Jun Lu; Guiling Mo; Yaojun Ling; Lijuan Ji
Journal:  Mol Med Rep       Date:  2016-08-26       Impact factor: 2.952

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