Literature DB >> 15258833

A 1-Mb critical region in six patients with 9q34.3 terminal deletion syndrome.

Naoki Harada1,2,3, Remco Visser1,4,5, Angie Dawson6, Makoto Fukamachi7, Mie Iwakoshi8, Nobuhiko Okamoto9, Tatsuya Kishino2,10, Norio Niikawa1,2, Naomichi Matsumoto11,12,13.   

Abstract

Patients with 9q34.3 terminal deletion usually show a clinically recognizable phenotype characterized by specific facial features (microcephaly, flat face, arched eyebrows, hypertelorism, short nose, anteverted nostrils, carp mouth and protruding tongue) in combination with severe mental retardation, hypotonia, and other anomalies. We analyzed six unrelated patients with a various 9q34.3 terminal deletion. While having different-sized 9q34.3 deletions, all of these patients shared several distinctive anomalies. These anomalies are likely to arise from a commonly deleted region at distal 9q34.3. Fluorescence in situ hybridization (FISH) analysis using a dozen BAC clones mapped at the 9q34.13-q34.3 region defined the shortest region of deletion overlap (SRO) as a 1-Mb segment proximal to 9qter containing eight known genes. Possible candidate genes delineating specific phenotypes of the 9q34.3 terminal deletion syndrome are discussed.

Entities:  

Mesh:

Year:  2004        PMID: 15258833     DOI: 10.1007/s10038-004-0166-z

Source DB:  PubMed          Journal:  J Hum Genet        ISSN: 1434-5161            Impact factor:   3.172


  15 in total

1.  Cryptic terminal deletion of chromosome 9q34: a novel cause of syndromic obesity in childhood?

Authors:  V Cormier-Daire; F Molinari; M Rio; O Raoul; M-C de Blois; S Romana; M Vekemans; A Munnich; L Colleaux
Journal:  J Med Genet       Date:  2003-04       Impact factor: 6.318

2.  Subtelomere specific microarray based comparative genomic hybridisation: a rapid detection system for cryptic rearrangements in idiopathic mental retardation.

Authors:  N Harada; E Hatchwell; N Okamoto; M Tsukahara; K Kurosawa; H Kawame; T Kondoh; H Ohashi; R Tsukino; Y Kondoh; O Shimokawa; T Ida; T Nagai; Y Fukushima; K Yoshiura; N Niikawa; N Matsumoto
Journal:  J Med Genet       Date:  2004-02       Impact factor: 6.318

3.  Improved telomere detection using a telomere repeat probe (TTAGGG)n generated by PCR.

Authors:  J W Ijdo; R A Wells; A Baldini; S T Reeders
Journal:  Nucleic Acids Res       Date:  1991-09-11       Impact factor: 16.971

4.  E2F-6, a member of the E2F family that can behave as a transcriptional repressor.

Authors:  J M Trimarchi; B Fairchild; R Verona; K Moberg; N Andon; J A Lees
Journal:  Proc Natl Acad Sci U S A       Date:  1998-03-17       Impact factor: 11.205

5.  Homozygosity mapping in families with Joubert syndrome identifies a locus on chromosome 9q34.3 and evidence for genetic heterogeneity.

Authors:  K Saar; L Al-Gazali; L Sztriha; F Rueschendorf; M Nur-E-Kamal; A Reis; R Bayoumi
Journal:  Am J Hum Genet       Date:  1999-12       Impact factor: 11.025

6.  A PKC epsilon-ENH-channel complex specifically modulates N-type Ca2+ channels.

Authors:  Yuka Maeno-Hikichi; Shaohua Chang; Kiyoyuki Matsumura; Meizan Lai; Hong Lin; Noritaka Nakagawa; Shun'ichi Kuroda; Ji-fang Zhang
Journal:  Nat Neurosci       Date:  2003-05       Impact factor: 24.884

7.  MIZIP, a highly conserved, vertebrate specific melanin-concentrating hormone receptor 1 interacting zinc-finger protein.

Authors:  Dietmar Bächner; Hans-Jürgen Kreienkamp; Dietmar Richter
Journal:  FEBS Lett       Date:  2002-08-28       Impact factor: 4.124

Review 8.  9q34.3 deletion syndrome in three unrelated children.

Authors:  Mie Iwakoshi; Nobuhiko Okamoto; Naoki Harada; Tsuyoshi Nakamura; Shunji Yamamori; Hiroko Fujita; Norio Niikawa; Naomichi Matsumoto
Journal:  Am J Med Genet A       Date:  2004-04-30       Impact factor: 2.802

Review 9.  Uniparental disomy in humans: development of an imprinting map and its implications for prenatal diagnosis.

Authors:  D H Ledbetter; E Engel
Journal:  Hum Mol Genet       Date:  1995       Impact factor: 6.150

10.  Cryptic chromosome rearrangements detected by subtelomere assay in patients with mental retardation and dysmorphic features.

Authors:  A J Dawson; S Putnam; J Schultz; D Riordan; C Prasad; C R Greenberg; B N Chodirker; A A Mhanni; A E Chudley
Journal:  Clin Genet       Date:  2002-12       Impact factor: 4.438

View more
  10 in total

1.  Molecular mechanisms for subtelomeric rearrangements associated with the 9q34.3 microdeletion syndrome.

Authors:  Svetlana A Yatsenko; Ellen K Brundage; Erin K Roney; Sau Wai Cheung; A Craig Chinault; James R Lupski
Journal:  Hum Mol Genet       Date:  2009-03-17       Impact factor: 6.150

2.  Loss-of-function mutations in euchromatin histone methyl transferase 1 (EHMT1) cause the 9q34 subtelomeric deletion syndrome.

Authors:  Tjitske Kleefstra; Han G Brunner; Jeanne Amiel; Astrid R Oudakker; Willy M Nillesen; Alex Magee; David Geneviève; Valérie Cormier-Daire; Hilde van Esch; Jean-Pierre Fryns; Ben C J Hamel; Erik A Sistermans; Bert B A de Vries; Hans van Bokhoven
Journal:  Am J Hum Genet       Date:  2006-06-13       Impact factor: 11.025

3.  Mutation of zebrafish Snapc4 is associated with loss of the intrahepatic biliary network.

Authors:  Madeline Schaub; Justin Nussbaum; Heather Verkade; Elke A Ober; Didier Y R Stainier; Takuya F Sakaguchi
Journal:  Dev Biol       Date:  2011-12-23       Impact factor: 3.582

4.  Update on Kleefstra Syndrome.

Authors:  M H Willemsen; A T Vulto-van Silfhout; W M Nillesen; W M Wissink-Lindhout; H van Bokhoven; N Philip; E M Berry-Kravis; U Kini; C M A van Ravenswaaij-Arts; B Delle Chiaie; A M M Innes; G Houge; T Kosonen; K Cremer; M Fannemel; A Stray-Pedersen; W Reardon; J Ignatius; K Lachlan; C Mircher; P T J M Helderman van den Enden; M Mastebroek; P E Cohn-Hokke; H G Yntema; S Drunat; T Kleefstra
Journal:  Mol Syndromol       Date:  2012-01-24

Review 5.  Cytogenomic Aberrations in Congenital Cardiovascular Malformations.

Authors:  Mahshid Azamian; Seema R Lalani
Journal:  Mol Syndromol       Date:  2016-04-26

6.  Phenotype and variations associated with the deletion of the 1q44 cytoband and the pathogenic duplication in the 9q32q34.3 cytobands.

Authors:  Ana Gómez-Carpintero García; Ana Vidal Esteban; Amanda Bermejo Gómez; Ruth Camila Púa Torrejón
Journal:  BMJ Case Rep       Date:  2020-03-08

Review 7.  Reprogramming of the epigenome in neurodevelopmental disorders.

Authors:  Khadija D Wilson; Elizabeth G Porter; Benjamin A Garcia
Journal:  Crit Rev Biochem Mol Biol       Date:  2021-10-02       Impact factor: 8.697

Review 8.  Histone Lysine Methylation and Neurodevelopmental Disorders.

Authors:  Jeong-Hoon Kim; Jang Ho Lee; Im-Soon Lee; Sung Bae Lee; Kyoung Sang Cho
Journal:  Int J Mol Sci       Date:  2017-06-30       Impact factor: 5.923

Review 9.  The sociability spectrum: evidence from reciprocal genetic copy number variations.

Authors:  Alejandro López-Tobón; Sebastiano Trattaro; Giuseppe Testa
Journal:  Mol Autism       Date:  2020-06-16       Impact factor: 7.509

10.  Genetic Imbalances in Argentinean Patients with Congenital Conotruncal Heart Defects.

Authors:  Marisol Delea; Lucía D Espeche; Carlos D Bruque; María Paz Bidondo; Lucía S Massara; Jaen Oliveri; Paloma Brun; Viviana R Cosentino; Celeste Martinoli; Norma Tolaba; Claudina Picon; María Eugenia Ponce Zaldua; Silvia Ávila; Viviana Gutnisky; Myriam Perez; Lilian Furforo; Noemí D Buzzalino; Rosa Liascovich; Boris Groisman; Mónica Rittler; Sandra Rozental; Pablo Barbero; Liliana Dain
Journal:  Genes (Basel)       Date:  2018-09-11       Impact factor: 4.096

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.