Growth retardation versus overgrowth:: Silver-Russell syndrome is genetically opposite to Beckwith-Wiedemann syndrome

被引:83
|
作者
Eggermann, Thomas [1 ]
Eggermann, Katja [1 ]
Schoenherr, Nadine [1 ]
机构
[1] Rhein Westfal TH Aachen, Inst Human Genet, D-52074 Aachen, Germany
关键词
D O I
10.1016/j.tig.2008.01.003
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Human growth is a complex process that requires the appropriate interaction of many players. Central members in the growth pathways are regulated epigenetically and thereby reflect the profound significance of imprinting for correct mammalian ontogenesis. In this review, we show that the growth retardation disorder Silver-Russell syndrome (SRS) is a suitable model to decipher the role of imprinting in growth. As we will show, SRS should not only be regarded as the genetically (and clinically) opposite disease to Beckwith-Wiedemann syndrome, but it also represents the first human disorder with imprinting disturbances that affect two different chromosomes (i.e. chromosomes 7 and 11). Thus, a functional interaction between factors encoded by chromosomes 7 and 11 is likely.
引用
收藏
页码:195 / 204
页数:10
相关论文
共 50 条
  • [2] Modeling human epigenetic disorders in mice: Beckwith-Wiedemann syndrome and Silver-Russell syndrome
    Chang, Suhee
    Bartolomei, Marisa S.
    DISEASE MODELS & MECHANISMS, 2020, 13 (05)
  • [3] Silver-Russell Syndrome and Beckwith-Wiedemann Syndrome Phenotypes Associated with 11p Duplication in a Single Family
    Cardarelli, Laura
    Sparago, Angela
    De Crescenzo, Agostina
    Nalesso, Elisa
    Zavan, Barbara
    Cubellis, Maria Vittoria
    Selicorni, Angelo
    Cavicchioli, Paola
    Pozzan, Giovanni Battista
    Petrella, Marilena
    Riccio, Andrea
    PEDIATRIC AND DEVELOPMENTAL PATHOLOGY, 2010, 13 (04) : 326 - 330
  • [4] Beckwith-Wiedemann and Silver-Russell syndromes: opposite developmental imbalances in imprinted regulators of placental function and embryonic growth
    Jacob, K. J.
    Robinson, W. P.
    Lefebvre, L.
    CLINICAL GENETICS, 2013, 84 (04) : 326 - 334
  • [5] Diagnostic testing for Beckwith-Wiedemann syndrome/Russell-Silver syndrome: The GGC experience
    Abidi, Fatima
    Fang, Xiaolan
    Fletcher, Robin
    Wang, Jiyong
    Jones, Julie
    Friez, Michael
    Lee, Jennifer
    GENETICS IN MEDICINE, 2022, 24 (03) : S196 - S196
  • [6] Discrepant molecular and clinical diagnoses in Beckwith-Wiedemann and Silver-Russell syndromes
    Mackay, Deborah J. G.
    Bliek, Jet
    Lombardi, Maria Paola
    Russo, Silvia
    Calzari, Luciano
    Guzzetti, Sara
    Izzi, Claudia
    Selicorni, Angelo
    Melis, Daniela
    Temple, Karen
    Maher, Eamonn
    Brioude, Frederic
    Netchine, Irene
    Eggermann, Thomas
    GENETICS RESEARCH, 2019, 101
  • [7] Need for a precise molecular diagnosis in Beckwith-Wiedemann and Silver-Russell syndrome: what has to be considered and why it is important
    Thomas Eggermann
    Johanna Brück
    Cordula Knopp
    György Fekete
    Christian Kratz
    Velibor Tasic
    Ingo Kurth
    Miriam Elbracht
    Katja Eggermann
    Matthias Begemann
    Journal of Molecular Medicine, 2020, 98 : 1447 - 1455
  • [8] Disruption of genomic neighbourhood at the imprinted IGF2-H19 locus in Beckwith-Wiedemann syndrome and Silver-Russell syndrome
    Nativio, Raffaella
    Sparago, Angela
    Ito, Yoko
    Weksberg, Rosanna
    Riccio, Andrea
    Murrell, Adele
    HUMAN MOLECULAR GENETICS, 2011, 20 (07) : 1363 - 1374
  • [9] Need for a precise molecular diagnosis in Beckwith-Wiedemann and Silver-Russell syndrome: what has to be considered and why it is important
    Eggermann, Thomas
    Bruck, Johanna
    Knopp, Cordula
    Fekete, Gyorgy
    Kratz, Christian
    Tasic, Velibor
    Kurth, Ingo
    Elbracht, Miriam
    Eggermann, Katja
    Begemann, Matthias
    JOURNAL OF MOLECULAR MEDICINE-JMM, 2020, 98 (10): : 1447 - 1455
  • [10] Case Studies of Two Classical Imprinting Growth Disorders: Silver-Russell and Beckwith-Wiedemann Syndromes
    Kaur, Parminder
    Chaudhry, Chakshu
    Kaur, Anupriya
    Panigrahi, Inusha
    Srivastava, Priyanka
    JOURNAL OF PEDIATRIC GENETICS, 2024, 13 (02) : 127 - 132