Literature DB >> 21595003

A microduplication on chromosome 17p13.1p13.3 including the PAFAH1B1 (LIS1) gene.

Kristiina Avela1, Katja Aktan-Collan, Nina Horelli-Kuitunen, Sakari Knuutila, Mirja Somer.   

Abstract

Recently, three children with a microduplication in 17p13 including the PAFAH1B1 gene that encodes LIS1 were reported. LIS1 overexpression has earlier been shown to affect brain development by causing migrational defects and reductions in brain volume [Bi et al., 2009]. Here, we report an additional patient with a microduplication on chromosome 17p13.1p13.3 including the PAFAH1B1 gene, that was inserted into the long arm of chromosome 4. The patient had psychomotor and growth retardation, dysmorphic features, small ventricular septal defect (VSD), and immunoglobulin abnormality. Only subtle abnormalities in brain MRI scan were seen. Interestingly, the facial features of our patient closely resemble those previously reported in 17p trisomy patients.

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Year:  2011        PMID: 21595003     DOI: 10.1002/ajmg.a.33944

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  9 in total

1.  Regulation of neuronal morphogenesis by 14-3-3epsilon (Ywhae) via the microtubule binding protein, doublecortin.

Authors:  Brett Cornell; Tomoka Wachi; Vladimir Zhukarev; Kazuhito Toyo-Oka
Journal:  Hum Mol Genet       Date:  2016-10-15       Impact factor: 6.150

2.  Clinical and Molecular Cytogenetic Characterisation of Children with Developmental Delay and Dysmorphic Features.

Authors:  Sara Bertok; Mojca Žerjav Tanšek; Primož Kotnik; Tadej Battelino; Marija Volk; Vanna Pecile; Lisa Cleva; Paolo Gasparini; Jernej Kovač; Tinka Hovnik
Journal:  Zdr Varst       Date:  2015-03-13

3.  Case Report: First Case of Non-restrictive Ventricular Septal Defect With Congestive Heart Failure in a Chinese Han Male Infant Carrying a Class II Chromosome 17p13.3 Microduplication.

Authors:  Yung-Yu Yang; Chun-Ting Liu; Li-Fan Pai; Chih-Fen Hu; Shyi-Jou Chen; Wan-Fu Hsu
Journal:  Front Pediatr       Date:  2022-02-28       Impact factor: 3.418

4.  [Application of single nucleotide polymorphism microarray in clinical diagnosis of intellectual disability or retardation].

Authors:  Junjie Hu; Yeqing Qian; Yixi Sun; Jialing Yu; Yuqin Luo; Minyue Dong
Journal:  Zhejiang Da Xue Xue Bao Yi Xue Ban       Date:  2019-06-25

5.  Prenatal diagnosis of 17p13.1p13.3 duplication.

Authors:  Kirsi Kiiski; Tiiu Roovere; Riina Zordania; Harriet von Koskull; Nina Horelli-Kuitunen
Journal:  Case Rep Med       Date:  2012-10-17

6.  A cryptic balanced translocation (5;17), a puzzle revealed through a critical evaluation of the pedigree and a FISH focused on candidate loci suggested by the phenotype.

Authors:  N Perrotti; Paola Malatesta; A Primerano; E Colao; C Villella; M D Nocera; A Ciambrone; E Luciano; L D'Antona; M F M Vismara; S Loddo; A Novelli
Journal:  Mol Cytogenet       Date:  2015-09-02       Impact factor: 2.009

Review 7.  LIS1 and DCX: Implications for Brain Development and Human Disease in Relation to Microtubules.

Authors:  Orly Reiner
Journal:  Scientifica (Cairo)       Date:  2013-03-17

Review 8.  14-3-3 Proteins in Brain Development: Neurogenesis, Neuronal Migration and Neuromorphogenesis.

Authors:  Brett Cornell; Kazuhito Toyo-Oka
Journal:  Front Mol Neurosci       Date:  2017-10-12       Impact factor: 5.639

Review 9.  Responsible Genes for Neuronal Migration in the Chromosome 17p13.3: Beyond Pafah1b1(Lis1), Crk and Ywhae(14-3-3ε).

Authors:  Xiaonan Liu; Sarah A Bennison; Lozen Robinson; Kazuhito Toyo-Oka
Journal:  Brain Sci       Date:  2021-12-30
  9 in total

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