Literature DB >> 24550762

Currarino Syndrome and HPE Microform Associated with a 2.7-Mb Deletion in 7q36.3 Excluding SHH Gene.

C Coutton1, B Poreau2, F Devillard3, C Durand4, S Odent5, C Rozel6, G Vieville3, F Amblard3, P-S Jouk2, V Satre1.   

Abstract

Holoprosencephaly (HPE) is the most common forebrain defect in humans. It results from incomplete midline cleavage of the prosencephalon and can be caused by environmental and genetic factors. HPE is usually described as a continuum of brain malformations from the most severe alobar HPE to the middle interhemispheric fusion variant or syntelencephaly. A microform of HPE is limited to craniofacial features such as congenital nasal pyriform aperture stenosis and single central maxillary incisor, without brain malformation. Among the heterogeneous causes of HPE, point mutations and deletions in the SHH gene at 7q36 have been identified as well as extremely rare chromosomal rearrangements in the long-range enhancers of this gene. Here, we report a boy with an HPE microform associated with a Currarino syndrome. Array CGH detected a de novo 2.7-Mb deletion in the 7q36.3 region including the MNX1 gene, usually responsible for the Currarino triad but excluding SHH, which is just outside the deletion. This new case provides further evidence of the importance of the SHH long-range enhancers in the HPE spectrum.

Entities:  

Keywords:  Currarino syndrome; Holoprosencephaly; Long-range enhancers; Microdeletion 7q36; Sonic hedgehog

Year:  2013        PMID: 24550762      PMCID: PMC3919490          DOI: 10.1159/000355391

Source DB:  PubMed          Journal:  Mol Syndromol        ISSN: 1661-8769


  29 in total

1.  New findings for phenotype-genotype correlations in a large European series of holoprosencephaly cases.

Authors:  Sandra Mercier; Christèle Dubourg; Nicolas Garcelon; Boris Campillo-Gimenez; Isabelle Gicquel; Marion Belleguic; Leslie Ratié; Laurent Pasquier; Philippe Loget; Claude Bendavid; Sylvie Jaillard; Lucie Rochard; Chloé Quélin; Valérie Dupé; Véronique David; Sylvie Odent
Journal:  J Med Genet       Date:  2011-09-22       Impact factor: 6.318

2.  A gene for autosomal dominant sacral agenesis maps to the holoprosencephaly region at 7q36.

Authors:  S A Lynch; P M Bond; A J Copp; W O Kirwan; S Nour; R Balling; E Mariman; J Burn; T Strachan
Journal:  Nat Genet       Date:  1995-09       Impact factor: 38.330

3.  Novel mutations in the MNX1 gene in two families with Currarino syndrome and variable phenotype.

Authors:  Ellen Markljung; Tatjana Adamovic; Jia Cao; Hussein Naji; Sylvie Kaiser; Tomas Wester; Agneta Nordenskjöld
Journal:  Gene       Date:  2012-07-20       Impact factor: 3.688

Review 4.  De novo deletion 7q36 resulting from a distal 7q/8q translocation: phenotypic expression and comparison to the literature.

Authors:  T Lukusa; J R Vermeesch; J P Fryns
Journal:  Genet Couns       Date:  2005

5.  Exome sequencing reveals DNAJB6 mutations in dominantly-inherited myopathy.

Authors:  Matthew B Harms; R Brian Sommerville; Peggy Allred; Shaughn Bell; Duanduan Ma; Paul Cooper; Glenn Lopate; Alan Pestronk; Conrad C Weihl; Robert H Baloh
Journal:  Ann Neurol       Date:  2012-02-14       Impact factor: 10.422

Review 6.  cis-regulatory mutations are a genetic cause of human limb malformations.

Authors:  Julia E VanderMeer; Nadav Ahituv
Journal:  Dev Dyn       Date:  2011-01-11       Impact factor: 3.780

7.  Spectrum of HLXB9 gene mutations in Currarino syndrome and genotype-phenotype correlation.

Authors:  C Crétolle; A Pelet; D Sanlaville; M Zérah; J Amiel; F Jaubert; Y Révillon; L Baala; A Munnich; C Nihoul-Fékété; S Lyonnet
Journal:  Hum Mutat       Date:  2008-07       Impact factor: 4.878

8.  Regulation of a remote Shh forebrain enhancer by the Six3 homeoprotein.

Authors:  Yongsu Jeong; Federico Coluccio Leskow; Kenia El-Jaick; Erich Roessler; Maximilian Muenke; Anastasia Yocum; Christele Dubourg; Xue Li; Xin Geng; Guillermo Oliver; Douglas J Epstein
Journal:  Nat Genet       Date:  2008-10-05       Impact factor: 38.330

Review 9.  Structural and functional diversities between members of the human HSPB, HSPH, HSPA, and DNAJ chaperone families.

Authors:  Michel J Vos; Jurre Hageman; Serena Carra; Harm H Kampinga
Journal:  Biochemistry       Date:  2008-06-17       Impact factor: 3.162

10.  Mutations affecting the cytoplasmic functions of the co-chaperone DNAJB6 cause limb-girdle muscular dystrophy.

Authors:  Jaakko Sarparanta; Per Harald Jonson; Christelle Golzio; Satu Sandell; Helena Luque; Mark Screen; Kristin McDonald; Jeffrey M Stajich; Ibrahim Mahjneh; Anna Vihola; Olayinka Raheem; Sini Penttilä; Sara Lehtinen; Sanna Huovinen; Johanna Palmio; Giorgio Tasca; Enzo Ricci; Peter Hackman; Michael Hauser; Nicholas Katsanis; Bjarne Udd
Journal:  Nat Genet       Date:  2012-02-26       Impact factor: 38.330

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  5 in total

1.  Spectrum of MNX1 Pathogenic Variants and Associated Clinical Features in Korean Patients with Currarino Syndrome.

Authors:  Seungjun Lee; Eun Jin Kim; Sung Im Cho; Hyunwoong Park; Soo Hyun Seo; Moon Woo Seong; Sung Sup Park; Sung Eun Jung; Seong Cheol Lee; Kwi Won Park; Hyun Young Kim
Journal:  Ann Lab Med       Date:  2018-05       Impact factor: 3.464

2.  Currarino syndrome and microcephaly due to a rare 7q36.2 microdeletion: a case report.

Authors:  Lucia Cococcioni; Susanna Paccagnini; Elena Pozzi; Luigina Spaccini; Elisa Cattaneo; Serena Redaelli; Francesca Crosti; Gian Vincenzo Zuccotti
Journal:  Ital J Pediatr       Date:  2018-05-25       Impact factor: 2.638

3.  Novel MNX1 mutations and genotype-phenotype analysis of patients with Currarino syndrome.

Authors:  Lu Han; Zhen Zhang; Hui Wang; Hui Song; Qing Gao; Yuchun Yan; Ran Tao; Ping Xiao; Long Li; Qian Jiang; Qi Li
Journal:  Orphanet J Rare Dis       Date:  2020-06-22       Impact factor: 4.123

Review 4.  Currarino syndrome: a comprehensive genetic review of a rare congenital disorder.

Authors:  Gabriel C Dworschak; Heiko M Reutter; Michael Ludwig
Journal:  Orphanet J Rare Dis       Date:  2021-04-09       Impact factor: 4.123

5.  Case Report: Congenital Brain Dysplasia, Developmental Delay and Intellectual Disability in a Patient With a 7q35-7q36.3 Deletion.

Authors:  Liang-Liang Fan; Yue Sheng; Chen-Yu Wang; Ya-Li Li; Ji-Shi Liu
Journal:  Front Genet       Date:  2021-12-01       Impact factor: 4.599

  5 in total

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