Literature DB >> 27761175

MR Imaging Findings in Xp21.2 Duplication Syndrome.

Matthew T Whitehead1, Guy Helman2, Andrea L Gropman2.   

Abstract

Xp21.2 duplication syndrome is a rare genetic disorder of undetermined prevalence and clinical relevance. As the use of chromosomal microarray has become first line for the work-up of childhood developmental delay, more gene deletions and duplications have been recognized. To the best of our knowledge, the imaging findings of Xp21.2 duplication syndrome have not been reported. We report a case of a 33 month-old male referred for developmental delay that was found to have an Xp21.2 duplication containing IL1RAPL1 and multiple midline brain malformations.

Entities:  

Keywords:  Xq21.2 duplication; corpus callosum; fornix; hypothalamus; olfactory; vermis

Mesh:

Year:  2016        PMID: 27761175      PMCID: PMC5065289          DOI: 10.3941/jrcr.v10i5.2563

Source DB:  PubMed          Journal:  J Radiol Case Rep        ISSN: 1943-0922


  11 in total

1.  Molecular and clinical characterization of a small duplication Xp in a human female with psychiatric disorders.

Authors:  Maria Piccione; Cinzia Sanfilippo; Simona Cavani; Patrizia Salatiello; Michela Malacarne; Mauro Pierluigi; Marco Fichera; Daniela Luciano; Giovanni Corsello
Journal:  J Genet       Date:  2011-12       Impact factor: 1.166

2.  Copy-number variations on the X chromosome in Japanese patients with mental retardation detected by array-based comparative genomic hybridization analysis.

Authors:  Shozo Honda; Shin Hayashi; Issei Imoto; Jun Toyama; Hitoshi Okazawa; Eiji Nakagawa; Yu-Ichi Goto; Johji Inazawa
Journal:  J Hum Genet       Date:  2010-07-08       Impact factor: 3.172

3.  IL-1 receptor accessory protein-like 1 associated with mental retardation and autism mediates synapse formation by trans-synaptic interaction with protein tyrosine phosphatase δ.

Authors:  Tomoyuki Yoshida; Misato Yasumura; Takeshi Uemura; Sung-Jin Lee; Moonjin Ra; Ryo Taguchi; Yoichiro Iwakura; Masayoshi Mishina
Journal:  J Neurosci       Date:  2011-09-21       Impact factor: 6.167

4.  A new member of the IL-1 receptor family highly expressed in hippocampus and involved in X-linked mental retardation.

Authors:  A Carrié; L Jun; T Bienvenu; M C Vinet; N McDonell; P Couvert; R Zemni; A Cardona; G Van Buggenhout; S Frints; B Hamel; C Moraine; H H Ropers; T Strom; G R Howell; A Whittaker; M T Ross; A Kahn; J P Fryns; C Beldjord; P Marynen; J Chelly
Journal:  Nat Genet       Date:  1999-09       Impact factor: 38.330

Review 5.  Common fragile sites, extremely large genes, neural development and cancer.

Authors:  David I Smith; Yu Zhu; Sarah McAvoy; Robert Kuhn
Journal:  Cancer Lett       Date:  2005-10-10       Impact factor: 8.679

6.  Mapping of a gene for non-specific X linked mental retardation: evidence for linkage to chromosomal region Xp21.1-Xp22.3.

Authors:  L Kozák; P Chiurazzi; M Genuardi; M G Pomponi; M Zollino; G Neri
Journal:  J Med Genet       Date:  1993-10       Impact factor: 6.318

7.  Novel mutation of IL1RAPL1 gene in a nonspecific X-linked mental retardation (MRX) family.

Authors:  Magdalena Nawara; Jakub Klapecki; Katarzyna Borg; Marta Jurek; Sarah Moreno; Jolanta Tryfon; Jerzy Bal; Jamel Chelly; Tadeusz Mazurczak
Journal:  Am J Med Genet A       Date:  2008-12-15       Impact factor: 2.802

8.  Isolated 46,XY gonadal dysgenesis in two sisters caused by a Xp21.2 interstitial duplication containing the DAX1 gene.

Authors:  Michela Barbaro; Mikael Oscarson; Jacqueline Schoumans; Johan Staaf; Sten A Ivarsson; Anna Wedell
Journal:  J Clin Endocrinol Metab       Date:  2007-05-15       Impact factor: 5.958

9.  Tuber cinereum diverticula in a 28-month-old with xq21 deletion syndrome.

Authors:  Matthew T Whitehead; Gilbert Vezina
Journal:  Case Rep Radiol       Date:  2014-07-13

10.  Efficient strategy for the molecular diagnosis of intellectual disability using targeted high-throughput sequencing.

Authors:  Claire Redin; Bénédicte Gérard; Julia Lauer; Yvan Herenger; Jean Muller; Angélique Quartier; Alice Masurel-Paulet; Marjolaine Willems; Gaétan Lesca; Salima El-Chehadeh; Stéphanie Le Gras; Serge Vicaire; Muriel Philipps; Michaël Dumas; Véronique Geoffroy; Claire Feger; Nicolas Haumesser; Yves Alembik; Magalie Barth; Dominique Bonneau; Estelle Colin; Hélène Dollfus; Bérénice Doray; Marie-Ange Delrue; Valérie Drouin-Garraud; Elisabeth Flori; Mélanie Fradin; Christine Francannet; Alice Goldenberg; Serge Lumbroso; Michèle Mathieu-Dramard; Dominique Martin-Coignard; Didier Lacombe; Gilles Morin; Anne Polge; Sylvie Sukno; Christel Thauvin-Robinet; Julien Thevenon; Martine Doco-Fenzy; David Genevieve; Pierre Sarda; Patrick Edery; Bertrand Isidor; Bernard Jost; Laurence Olivier-Faivre; Jean-Louis Mandel; Amélie Piton
Journal:  J Med Genet       Date:  2014-08-28       Impact factor: 6.318

View more
  1 in total

1.  Identification of microduplications at Xp21.2 and Xq13.1 in neurodevelopmental disorders.

Authors:  Hannaleena Kokkonen; Auli Siren; Tuomo Määttä; Magda Kamila Kadlubowska; Anushree Acharya; Liz M Nouel-Saied; Suzanne M Leal; Irma Järvelä; Isabelle Schrauwen
Journal:  Mol Genet Genomic Med       Date:  2021-05-12       Impact factor: 2.473

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.