Literature DB >> 1285376

Kabuki make-up (Niikawa-Kuroki) syndrome: a study of 16 non-Japanese cases.

N Philip1, P Meinecke, A David, J Dean, S Ayme, R Clark, E Gross-Kieselstein, D Hosenfeld, A Moncla, D Muller.   

Abstract

Kabuki make-up (Niikawa-Kuroki) syndrome has been described mainly in Japanese patients. In this paper we report sixteen new cases from Europe and North America, suggesting that Kabuki make-up syndrome may be more common outside of Japan than supposed. Their features are compared with those of the Japanese patients and most of our findings are similar to those previously reported. The facial phenotype is specific and easily recognizable, regardless of ethnic origin. Postnatal growth retardation and mild mental retardation are confirmed to be cardinal manifestations of the syndrome. Skeletal anomalies were present in all cases but most of the radiological changes were non-specific. The specificity of metacarpophalangeal pattern profile is not confirmed. Conversely, dermatoglyphic analysis is helpful in the diagnosis of this condition. Two differences have emerged between the Japanese patients and those in this study. Firstly, two-thirds of the patients in this series had significant neurological dysfunction other than mental retardation. Secondly, joint hypermobility appears more common in non-Japanese patients. Confirmation of these findings requires further studies.

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Year:  1992        PMID: 1285376

Source DB:  PubMed          Journal:  Clin Dysmorphol        ISSN: 0962-8827            Impact factor:   0.816


  15 in total

1.  Molecularly confirmed Kabuki (Niikawa-Kuroki) syndrome patients demonstrate a specific cognitive profile with extensive visuospatial abnormalities.

Authors:  J Harris; E M Mahone; H T Bjornsson
Journal:  J Intellect Disabil Res       Date:  2019-02-14

2.  Kabuki syndrome-like features in monozygotic twin boys with a pseudodicentric chromosome 13.

Authors:  S A Lynch; K A Ashcroft; S Zwolinski; C Clarke; J Burn
Journal:  J Med Genet       Date:  1995-03       Impact factor: 6.318

3.  Three patients with ring (X) chromosomes and a severe phenotype.

Authors:  N R Dennis; A L Collins; J A Crolla; A E Cockwell; A M Fisher; P A Jacobs
Journal:  J Med Genet       Date:  1993-06       Impact factor: 6.318

4.  The Kabuki (Niikawa-Kuroki) syndrome: further delineation of the phenotype in 29 non-Japanese patients.

Authors:  C Schrander-Stumpel; P Meinecke; G Wilson; G Gillessen-Kaesbach; S Tinschert; R König; N Philip; R Rizzo; J Schrander; L Pfeiffer
Journal:  Eur J Pediatr       Date:  1994-06       Impact factor: 3.183

5.  Infrequent Manifestations of Kabuki Syndrome in a Patient with Novel MLL2 Mutation.

Authors:  Y A Zarate; H Zhan; J R Jones
Journal:  Mol Syndromol       Date:  2012-08-30

6.  Surgical treatment of hip dislocation in Kabuki syndrome: use of incomplete periacetabular osteotomy for posterior acetabular wall deficiency.

Authors:  Akifusa Wada; Tomoyuki Nakamura; Toru Yamaguchi; Haruhisa Yanagida; Kazuyuki Takamura; Yutaka Oketani; Hideaki Kubota; Toshio Fujii
Journal:  J Child Orthop       Date:  2012-07-24       Impact factor: 1.548

7.  Coarctation of the aorta in Kabuki syndrome.

Authors:  H E Hughes; S J Davies
Journal:  Arch Dis Child       Date:  1994-06       Impact factor: 3.791

8.  Facial Dysmorphisms, Macrodontia, Focal Epilepsy, and Thinning of the Corpus Callosum: A Rare Mild Form of Kabuki Syndrome.

Authors:  Valentina Bruni; Cristina Scozzafava; Maria Gnazzo; Francesca Parisi; Simona Sestito; Licia Pensabene; Antonio Novelli; Daniela Concolino
Journal:  J Pediatr Genet       Date:  2020-02-17

9.  Kabuki Syndrome and Anorectal Malformations: Implications for Diagnosis and Treatment.

Authors:  Sotirios Siminas; Colin Tennant Baillie; Richard Turnock
Journal:  European J Pediatr Surg Rep       Date:  2015-05-28

Review 10.  Dermatoglyphics in kidney diseases: a review.

Authors:  Buddhika T B Wijerathne; Robert J Meier; Sujatha S Salgado; Suneth B Agampodi
Journal:  Springerplus       Date:  2016-03-08
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