Literature DB >> 15691356

Kabuki syndrome: a review.

M P Adam1, L Hudgins.   

Abstract

Kabuki syndrome (KS) (Kabuki make-up syndrome, Niikawa-Kuroki syndrome) is a multiple malformation/mental retardation syndrome that was described initially in Japan but is now known to occur in many other ethnic groups. It is characterized by distinctive facial features (eversion of the lower lateral eyelid, arched eyebrows with the lateral one-third dispersed or sparse, depressed nasal tip, and prominent ears), skeletal anomalies, dermatoglyphic abnormalities, short stature, and mental retardation. A number of other manifestations involving other organ systems can aid in the diagnosis and management of KS. This review will focus on the diagnostic criteria, the common and rare features of KS by organ system, and the possible etiology of this interesting condition.

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Year:  2005        PMID: 15691356     DOI: 10.1111/j.1399-0004.2004.00348.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  48 in total

1.  How genetically heterogeneous is Kabuki syndrome?: MLL2 testing in 116 patients, review and analyses of mutation and phenotypic spectrum.

Authors:  Siddharth Banka; Ratna Veeramachaneni; William Reardon; Emma Howard; Sancha Bunstone; Nicola Ragge; Michael J Parker; Yanick J Crow; Bronwyn Kerr; Helen Kingston; Kay Metcalfe; Kate Chandler; Alex Magee; Fiona Stewart; Vivienne P M McConnell; Deirdre E Donnelly; Siren Berland; Gunnar Houge; Jenny E Morton; Christine Oley; Nicole Revencu; Soo-Mi Park; Sally J Davies; Andrew E Fry; Sally Ann Lynch; Harinder Gill; Susann Schweiger; Wayne W K Lam; John Tolmie; Shehla N Mohammed; Emma Hobson; Audrey Smith; Moira Blyth; Christopher Bennett; Pradeep C Vasudevan; Sixto García-Miñaúr; Alex Henderson; Judith Goodship; Michael J Wright; Richard Fisher; Richard Gibbons; Susan M Price; Deepthi C de Silva; I Karen Temple; Amanda L Collins; Katherine Lachlan; Frances Elmslie; Meriel McEntagart; Bruce Castle; Jill Clayton-Smith; Graeme C Black; Dian Donnai
Journal:  Eur J Hum Genet       Date:  2011-11-30       Impact factor: 4.246

2.  Kabuki syndrome: diagnostic and treatment considerations.

Authors:  Bethany D Kasdon; Judith E Fox
Journal:  Ment Health Fam Med       Date:  2012-09

3.  Case report: autistic disorder in Kabuki syndrome.

Authors:  Burcu Akin Sari; Kadri Karaer; Sahin Bodur; A Sebnem Soysal
Journal:  J Autism Dev Disord       Date:  2007-08-25

4.  Double aortic arch: an unreported anomaly with Kabuki syndrome.

Authors:  Sergio Moral; Flavio Zuccarino; Pablo Loma-Osorio
Journal:  Pediatr Cardiol       Date:  2008-08-07       Impact factor: 1.655

5.  Report of the First Clinical Case of a Moroccan Kabuki Patient with a Novel MLL2 Mutation.

Authors:  I Ratbi; N Fejjal; L Micale; B Augello; C Fusco; J Lyahyai; G Merla; A Sefiani
Journal:  Mol Syndromol       Date:  2013-01-30

6.  Refractory ITP in a patient with Kabuki syndrome: response to low-dose rituximab.

Authors:  Brian Kerr; Philip Murphy; John Quinn
Journal:  Int J Hematol       Date:  2017-01-30       Impact factor: 2.490

7.  Anesthesia management in a patient with kabuki syndrome.

Authors:  Yunus Oktay Atalay; Cengiz Kaya; Yasemin Burcu Ustun; Ali Haydar Sahinoglu
Journal:  Med Arch       Date:  2014-10-15

8.  The C20orf133 gene is disrupted in a patient with Kabuki syndrome.

Authors:  Nicole M C Maas; Tom Van de Putte; Cindy Melotte; Annick Francis; Constance T R M Schrander-Stumpel; Damien Sanlaville; David Genevieve; Stanislas Lyonnet; Boyan Dimitrov; Koenraad Devriendt; Jean-Pierre Fryns; Joris R Vermeesch
Journal:  BMJ Case Rep       Date:  2009-06-30

9.  Kabuki syndrome genes KMT2D and KDM6A: functional analyses demonstrate critical roles in craniofacial, heart and brain development.

Authors:  Peter M Van Laarhoven; Leif R Neitzel; Anita M Quintana; Elizabeth A Geiger; Elaine H Zackai; David E Clouthier; Kristin B Artinger; Jeffrey E Ming; Tamim H Shaikh
Journal:  Hum Mol Genet       Date:  2015-05-13       Impact factor: 6.150

10.  Trans-tail regulation of MLL4-catalyzed H3K4 methylation by H4R3 symmetric dimethylation is mediated by a tandem PHD of MLL4.

Authors:  Shilpa S Dhar; Sung-Hun Lee; Pu-Yeh Kan; Philipp Voigt; Li Ma; Xiaobing Shi; Danny Reinberg; Min Gyu Lee
Journal:  Genes Dev       Date:  2012-12-15       Impact factor: 11.361

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