Literature DB >> 10465145

Epilepsy and polymicrogyria in Kabuki make-up (Niikawa-Kuroki) syndrome.

G Di Gennaro1, C Condoluci, C Casali, O Ciccarelli, G Albertini.   

Abstract

Kabuki make-up syndrome is a rare dysmorphogenic disorder characterized by peculiar facial appearance (resembling the make-up of actors in Kabuki, the traditional Japanese theatre), skeletal anomalies, dermatoglyphic abnormalities, postnatal growth deficiency, and mental retardation. Central nervous system dysfunctions, other than mental retardation, are rarely reported; they include microcephaly, brachycephaly, early hypotonia, feeding disorders, subatrophy of the optic nerves, subarachnoid cyst, cerebellar and brainstem atrophy, and epilepsy. These manifestations appear to be more common in non-Japanese patients. Reported is an Italian child with phenotypical appearance of Kabuki make-up syndrome and partial epilepsy who demonstrated polymicrogyria on neuroimaging. This article is the first report of a gyration disorder in Kabuki make-up syndrome. The relationship between epilepsy and polymicrogyria in this patient is discussed.

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Mesh:

Year:  1999        PMID: 10465145     DOI: 10.1016/s0887-8994(99)00030-2

Source DB:  PubMed          Journal:  Pediatr Neurol        ISSN: 0887-8994            Impact factor:   3.372


  8 in total

Review 1.  Genetics of the polymicrogyria syndromes.

Authors:  A Jansen; E Andermann
Journal:  J Med Genet       Date:  2005-05       Impact factor: 6.318

2.  Bilateral perysilvian polymicrogyria in Chiari I malformation.

Authors:  Alberto Spalice; Pasquale Parisi; Mario Mastrangelo; Francesca De Luca; Alberto Verrotti; Paola Iannetti
Journal:  Childs Nerv Syst       Date:  2006-10-13       Impact factor: 1.475

3.  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

4.  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

5.  High Fat Diet Triggers a Reduction in Body Fat Mass in Female Mice Deficient for Utx demethylase.

Authors:  Kazushige Ota; Akiyoshi Komuro; Hisayuki Amano; Akinori Kanai; Kai Ge; Takeshi Ueda; Hitoshi Okada
Journal:  Sci Rep       Date:  2019-07-11       Impact factor: 4.379

6.  Kabuki syndrome and perisylvian cortical dysplasia in a Turkish girl.

Authors:  Yasemin Topcu; Erhan Bayram; Pakize Karaoglu; Uluc Yis; Semra Hız Kurul
Journal:  J Pediatr Neurosci       Date:  2013-09

7.  Precocious and Early Central Puberty in Children With Pre-existing Medical Conditions: A Single Center Study.

Authors:  Sarah Winter; Adélaïde Durand; Raja Brauner
Journal:  Front Pediatr       Date:  2019-02-14       Impact factor: 3.418

Review 8.  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

  8 in total

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