Literature DB >> 26208246

Use of targeted next-generation sequencing for molecular diagnosis of craniosynostosis: Identification of a novel de novo mutation of EFNB1.

Toshiyuki Yamamoto1, Naru Igarashi2, Keiko Shimojima1, Noriko Sangu1, Yuko Sakamoto3, Kazuaki Shimoji4, Shinichi Niijima2.   

Abstract

Craniofrontonasal syndrome (CFNS; MIM#304110) is characterized by asymmetric facial features with hypertelorism and a broad bifid nose due to synostosis of the coronal suture. CFNS shows a unique X-linked inheritance pattern (most affected patients are female and obligate male carriers exhibit a mild manifestation or no typical features at all) associated with the ephrin-B1 gene (EFNB1) located in the Xq13.1 region. In this study, we performed targeted, massively parallel sequencing using a next-generation sequencer, and identified a novel EFNB1 mutation, c.270_271delCA, in a Japanese female patient with craniosynostosis. Because subsequent Sanger sequencing identified no mutation in either parent, this mutation was determined to be de novo in origin. After obtaining molecular diagnosis, a retrospective clinical evaluation confirmed the clinical diagnosis of CFNS in this patient. Comprehensive molecular diagnosis using a next-generation sequencer would be beneficial for early diagnosis of the patients with undiagnosed craniosynostosis.
© 2015 Japanese Teratology Society.

Entities:  

Keywords:  craniofrontonasal syndrome; craniosynostosis; ephrin-B1; massively parallel sequencing; mutation; next-generation sequencer

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Year:  2016        PMID: 26208246     DOI: 10.1111/cga.12123

Source DB:  PubMed          Journal:  Congenit Anom (Kyoto)        ISSN: 0914-3505            Impact factor:   1.409


  3 in total

1.  Clinical Diagnosis of Mendelian Disorders Using a Comprehensive Gene-Targeted Panel Test for Next-Generation Sequencing.

Authors:  Tetsuya Okazaki; Megumi Murata; Masachika Kai; Kaori Adachi; Naoko Nakagawa; Noriko Kasagi; Wataru Matsumura; Yoshihiro Maegaki; Eiji Nanba
Journal:  Yonago Acta Med       Date:  2016-06-29       Impact factor: 1.641

2.  Novel PLA2G6 mutations associated with an exonic deletion due to non-allelic homologous recombination in a patient with infantile neuroaxonal dystrophy.

Authors:  Toshiyuki Yamamoto; Keiko Shimojima; Takashi Shibata; Mari Akiyama; Makio Oka; Tomoyuki Akiyama; Harumi Yoshinaga; Katsuhiro Kobayashi
Journal:  Hum Genome Var       Date:  2015-11-19

3.  Challenges in detecting genomic copy number aberrations using next-generation sequencing data and the eXome Hidden Markov Model: a clinical exome-first diagnostic approach.

Authors:  Toshiyuki Yamamoto; Keiko Shimojima; Yumiko Ondo; Katsumi Imai; Pin Fee Chong; Ryutaro Kira; Mitsuhiro Amemiya; Akira Saito; Nobuhiko Okamoto
Journal:  Hum Genome Var       Date:  2016-08-18
  3 in total

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