Literature DB >> 9285441

Kabuki make-up (Niikawa-Kuroki) syndrome: cognitive abilities and autistic features.

H H Ho1, L C Eaves.   

Abstract

Kabuki make-up syndrome (KMS), also known as Niikawa-Kuroki syndrome, is a rare malformation complex characterized by a peculiar facies with long palpebral fissures and partially everted lower eyelid, mental retardation, dwarfism, and skeletal and dermatoglyphic abnormalities. Four children from different ethnic groups presented with phenotypic manifestation of KMS. They showed variable degrees of learning disabilities, mental retardation, and autistic behavior. Two boys declined in IQ in early adolescence. In addition to being aware of the variable presentation of cognitive and behavioral characteristics in those already diagnosed, it is important to consider KMS when assessing dysmorphic children with learning disabilities and/or autism.

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Year:  1997        PMID: 9285441     DOI: 10.1111/j.1469-8749.1997.tb07470.x

Source DB:  PubMed          Journal:  Dev Med Child Neurol        ISSN: 0012-1622            Impact factor:   5.449


  6 in total

1.  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

2.  A mutation screen in patients with Kabuki syndrome.

Authors:  Yun Li; Nina Bögershausen; Yasemin Alanay; Pelin Ozlem Simsek Kiper; Nadine Plume; Katharina Keupp; Esther Pohl; Barbara Pawlik; Martin Rachwalski; Esther Milz; Michaela Thoenes; Beate Albrecht; Eva-Christina Prott; Margret Lehmkühler; Stephanie Demuth; Gülen Eda Utine; Koray Boduroglu; Katja Frankenbusch; Guntram Borck; Gabriele Gillessen-Kaesbach; Gökhan Yigit; Dagmar Wieczorek; Bernd Wollnik
Journal:  Hum Genet       Date:  2011-05-24       Impact factor: 4.132

3.  A Child with Kabuki Syndrome and Autism Spectrum Disorder.

Authors:  Mehmet Sertçelik; Çağatay Uğur; Aynur Şahin Aközel; Cihat Kağan Gürkan
Journal:  Noro Psikiyatr Ars       Date:  2016-09-01       Impact factor: 1.339

4.  De novo mutations in genes of mediator complex causing syndromic intellectual disability: mediatorpathy or transcriptomopathy?

Authors:  Alfonso Caro-Llopis; Monica Rosello; Carmen Orellana; Silvestre Oltra; Sandra Monfort; Sonia Mayo; Francisco Martinez
Journal:  Pediatr Res       Date:  2016-08-08       Impact factor: 3.756

Review 5.  Kabuki syndrome: clinical and molecular characteristics.

Authors:  Chong-Kun Cheon; Jung Min Ko
Journal:  Korean J Pediatr       Date:  2015-09-21

6.  Neurobehavioral features in individuals with Kabuki syndrome.

Authors:  Cristina Caciolo; Paolo Alfieri; Giorgia Piccini; Maria Cristina Digilio; Francesca Romana Lepri; Marco Tartaglia; Deny Menghini; Stefano Vicari
Journal:  Mol Genet Genomic Med       Date:  2018-03-13       Impact factor: 2.183

  6 in total

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