Literature DB >> 29301000

Developmental Defects Associated With DNA Copy Number Gain of Chromosome 2q33.1: A Case Report and Review of Literature.

Akshaya Gupta1, Jacob Yo2, Gengming Huang2, Lynn Soong3, Jianli Dong2.   

Abstract

Caspases play a vital role during apoptosis. In addition to apoptosis, caspases play a role in cytokine gene induction and work to inhibit apoptosis. In order for individuals to thrive with useful tissue growth, the rate of cell growth and division must surpass the rate of cell division. It is well established that excessive cell death of embryonic cells is a vital process occurring before structural abnormalities, regardless of their nature. Here we describe a 13-month-old male patient with a 4.7Mb interstitial duplication of chromosome 2q33.1. This duplication was identified by chromosomal microarray (CMA) which is the first-tier clinical diagnostic test to identify copy number variants (CNVs) for patients with unexplained developmental delay or intellectual disability. This patient presents with global developmental delay, especially in speech, language, hypotonia, and bilateral simian creases. The duplicated region contains several disease-causing genes. We believe that the phenotype in this patient's case was likely related to the gain of caspase 8 and 10 genes.

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Year:  2018        PMID: 29301000      PMCID: PMC6251611          DOI: 10.1093/labmed/lmx086

Source DB:  PubMed          Journal:  Lab Med        ISSN: 0007-5027


  15 in total

Review 1.  Functions of caspase 8: the identified and the mysterious.

Authors:  Guy S Salvesen; Craig M Walsh
Journal:  Semin Immunol       Date:  2014-05-21       Impact factor: 11.130

2.  Intragenic duplication--a novel causative mechanism for SATB2-associated syndrome.

Authors:  Agne Liedén; Malin Kvarnung; Daniel Nilssson; Ellika Sahlin; Elisabeth Syk Lundberg
Journal:  Am J Med Genet A       Date:  2014-09-23       Impact factor: 2.802

Review 3.  Old, new and emerging functions of caspases.

Authors:  S Shalini; L Dorstyn; S Dawar; S Kumar
Journal:  Cell Death Differ       Date:  2014-12-19       Impact factor: 15.828

Review 4.  Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.

Authors:  David T Miller; Margaret P Adam; Swaroop Aradhya; Leslie G Biesecker; Arthur R Brothman; Nigel P Carter; Deanna M Church; John A Crolla; Evan E Eichler; Charles J Epstein; W Andrew Faucett; Lars Feuk; Jan M Friedman; Ada Hamosh; Laird Jackson; Erin B Kaminsky; Klaas Kok; Ian D Krantz; Robert M Kuhn; Charles Lee; James M Ostell; Carla Rosenberg; Stephen W Scherer; Nancy B Spinner; Dimitri J Stavropoulos; James H Tepperberg; Erik C Thorland; Joris R Vermeesch; Darrel J Waggoner; Michael S Watson; Christa Lese Martin; David H Ledbetter
Journal:  Am J Hum Genet       Date:  2010-05-14       Impact factor: 11.025

5.  American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants.

Authors:  Hutton M Kearney; Erik C Thorland; Kerry K Brown; Fabiola Quintero-Rivera; Sarah T South
Journal:  Genet Med       Date:  2011-07       Impact factor: 8.822

6.  Knockdown of zebrafish Fancd2 causes developmental abnormalities via p53-dependent apoptosis.

Authors:  Ting Xi Liu; Niall G Howlett; Min Deng; David M Langenau; Karl Hsu; Jennifer Rhodes; John P Kanki; Alan D D'Andrea; A Thomas Look
Journal:  Dev Cell       Date:  2003-12       Impact factor: 12.270

7.  Stage-specific apoptosis, developmental delay, and embryonic lethality in mice homozygous for a targeted disruption in the murine Bloom's syndrome gene.

Authors:  N Chester; F Kuo; C Kozak; C D O'Hara; P Leder
Journal:  Genes Dev       Date:  1998-11-01       Impact factor: 11.361

8.  Molecular cloning and characterization of mouse caspase-8.

Authors:  K Sakamaki; S Tsukumo; S Yonehara
Journal:  Eur J Biochem       Date:  1998-04-15

9.  Interstitial duplication of 2q32.1-q33.3 in a patient with epilepsy, developmental delay, and autistic behavior.

Authors:  Daisuke Usui; Shino Shimada; Keiko Shimojima; Midori Sugawara; Hajime Kawasaki; Hideo Shigematu; Yukitoshi Takahashi; Yushi Inoue; Katsumi Imai; Toshiyuki Yamamoto
Journal:  Am J Med Genet A       Date:  2013-03-05       Impact factor: 2.802

Review 10.  SATB2-associated syndrome: Mechanisms, phenotype, and practical recommendations.

Authors:  Yuri A Zarate; Jennifer L Fish
Journal:  Am J Med Genet A       Date:  2016-10-24       Impact factor: 2.802

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