Literature DB >> 7277096

Kabuki make-up syndrome: a syndrome of mental retardation, unusual facies, large and protruding ears, and postnatal growth deficiency.

N Niikawa, N Matsuura, Y Fukushima, T Ohsawa, T Kajii.   

Abstract

A previously unrecognized mental retardation malformation syndrome was observed in five unrelated Japanese children. Consistent clinical features included moderate-to-severe mental retardation, progressive dwarfism of postnatal onset, a peculiar facies characterized by long palpebral fissures, with eversion of the lateral third of the lower eyelids, arched eyebrows, broad and depressed nasal tip, large prominent earlobes, short fifth fingers, abnormal dermatoglyphics including absence of digital triradius c or d, and frequent otitis media in infancy. Inconsistent abnormalities included epicanthal folds, cleft or high-arched palate, widely spaced teeth, low occipital hair line, scoliosis, and dislocation of the hip joint. Neither familial occurrence nor parental consanguinity was noted. The etiology of the malformation syndrome remains unknown.

Entities:  

Mesh:

Year:  1981        PMID: 7277096     DOI: 10.1016/s0022-3476(81)80255-7

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  94 in total

1.  Kabuki make-up syndrome.

Authors:  M L Kulkarni; Sudarshan K Shetty; V K Chandrasekar; Preethi M Kulkarni
Journal:  Indian J Pediatr       Date:  2004-09       Impact factor: 1.967

2.  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

3.  Kabuki syndrome: diagnostic and treatment considerations.

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

4.  Exploring by whole exome sequencing patients with initial diagnosis of Rubinstein-Taybi syndrome: the interconnections of epigenetic machinery disorders.

Authors:  Gloria Negri; Pamela Magini; Donatella Milani; Milena Crippa; Elisa Biamino; Maria Piccione; Stefano Sotgiu; Chiara Perrìa; Giuseppina Vitiello; Marina Frontali; Antonella Boni; Elisabetta Di Fede; Maria Chiara Gandini; Elisa Adele Colombo; Michael J Bamshad; Deborah A Nickerson; Joshua D Smith; Italia Loddo; Palma Finelli; Marco Seri; Tommaso Pippucci; Lidia Larizza; Cristina Gervasini
Journal:  Hum Genet       Date:  2019-02-26       Impact factor: 4.132

5.  A novel constellation of cardiac findings for Kabuki syndrome: hypoplastic left heart syndrome and partial anomalous pulmonary venous drainage.

Authors:  Raveen Shahdadpuri; Sally Ann Lynch; H Murchan; Colin J McMahon
Journal:  Pediatr Cardiol       Date:  2008-02-19       Impact factor: 1.655

6.  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

Review 7.  Epigenetics, autism spectrum, and neurodevelopmental disorders.

Authors:  Sampathkumar Rangasamy; Santosh R D'Mello; Vinodh Narayanan
Journal:  Neurotherapeutics       Date:  2013-10       Impact factor: 7.620

8.  Precocious chondrocyte differentiation disrupts skeletal growth in Kabuki syndrome mice.

Authors:  Jill A Fahrner; Wan-Ying Lin; Ryan C Riddle; Leandros Boukas; Valerie B DeLeon; Sheetal Chopra; Susan E Lad; Teresa Romeo Luperchio; Kasper D Hansen; Hans T Bjornsson
Journal:  JCI Insight       Date:  2019-10-17

9.  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

10.  Comparative analysis of RNA-Seq alignment algorithms and the RNA-Seq unified mapper (RUM).

Authors:  Gregory R Grant; Michael H Farkas; Angel D Pizarro; Nicholas F Lahens; Jonathan Schug; Brian P Brunk; Christian J Stoeckert; John B Hogenesch; Eric A Pierce
Journal:  Bioinformatics       Date:  2011-07-19       Impact factor: 6.937

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.