Literature DB >> 16643546

Kabuki syndrome: oral and general features seen in a 2-year-old Chinese boy.

M Atar1, W Lee, D O'Donnell.   

Abstract

This report describes the case of a young Chinese boy with Kabuki syndrome (KS). KS is a congenital condition characterized by multiple anomalies, especially of the face, and is usually associated with mild to moderate mental retardation. The patient presented with the characteristic facial features of KS and some skeletal and neurological anomalies including a butterfly vertebrae with scoliosis, cerebral atrophy, and irregular dentition. Dental examination revealed screwdriver-shaped incisors and a high arched maxilla, features typical of patients with KS, as well as very poor oral hygiene and early childhood caries. This report includes discussion of the aetiology of KS as well as discussion of the long-term prognosis for this particular patient, and patients with KS in general, with consideration of associated dental and medical issues.

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Year:  2006        PMID: 16643546     DOI: 10.1111/j.1365-263X.2006.00699.x

Source DB:  PubMed          Journal:  Int J Paediatr Dent        ISSN: 0960-7439            Impact factor:   3.455


  6 in total

Review 1.  Kabuki syndrome: a Chinese case series and systematic review of the spectrum of mutations.

Authors:  Shuang Liu; Xiafei Hong; Cheng Shen; Quan Shi; Jian Wang; Feng Xiong; Zhengqing Qiu
Journal:  BMC Med Genet       Date:  2015-04-21       Impact factor: 2.103

Review 2.  Butterfly Vertebrae: A Systematic Review of the Literature and Analysis.

Authors:  Yoshihiro Katsuura; Han Jo Kim
Journal:  Global Spine J       Date:  2018-09-18

3.  Orofacial features and medical profile of eight individuals with Kabuki syndrome.

Authors:  N Silva-Andrade; K López-Ortega; M Gallottini
Journal:  Med Oral Patol Oral Cir Bucal       Date:  2019-09-01

Review 4.  Kabuki Syndrome-Clinical Review with Molecular Aspects.

Authors:  Snir Boniel; Krystyna Szymańska; Robert Śmigiel; Krzysztof Szczałuba
Journal:  Genes (Basel)       Date:  2021-03-25       Impact factor: 4.096

5.  KMT2D deficiency disturbs the proliferation and cell cycle activity of dental epithelial cell line (LS8) partially via Wnt signaling.

Authors:  Liping Pang; Hua Tian; Xuejun Gao; Weiping Wang; Xiaoyan Wang; Zhichun Zhang
Journal:  Biosci Rep       Date:  2021-11-26       Impact factor: 3.840

Review 6.  Clinical heterogeneity of Kabuki syndrome in a cohort of Italian patients and review of the literature.

Authors:  Francesca Di Candia; Paolo Fontana; Pamela Paglia; Mariateresa Falco; Carmen Rosano; Carmelo Piscopo; Gerarda Cappuccio; Maria Anna Siano; Daniele De Brasi; Claudia Mandato; Ilaria De Maggio; Gabriella Maria Squeo; Matteo Della Monica; Gioacchino Scarano; Fortunato Lonardo; Pietro Strisciuglio; Giuseppe Merla; Daniela Melis
Journal:  Eur J Pediatr       Date:  2021-07-07       Impact factor: 3.183

  6 in total

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