Microcephaly with a simplified gyral pattern in a child with a de novo TUBA1A variant

被引:5
|
作者
Wei, Heming [1 ]
Krishnappa, Janardhan [2 ,3 ]
Lin, Grace [1 ]
Kavalloor, Nirmal [4 ]
Lim, Jiin Ying [5 ]
Goh, Chew-Yin Jasmine [6 ]
Jamuar, Saumya Shekhar [3 ,5 ]
Thomas, Terrence [2 ,3 ]
Tan, Ene Choo [1 ,3 ]
机构
[1] KK Womens & Childrens Hosp, Res Lab, 100 Bukit Timah Rd, Singapore 229899, Singapore
[2] KK Womens & Childrens Hosp, Dept Paediat, Neurol Serv, Singapore, Singapore
[3] SingHlth Duke NUS Med Sch, Paediat Acad Clin Programme, Singapore, Singapore
[4] KK Womens & Childrens Hosp, Dept Neonatol, Singapore, Singapore
[5] KK Womens & Childrens Hosp, Dept Paediat, Genet Serv, Singapore, Singapore
[6] KK Womens & Childrens Hosp, Div Nursing, Singapore, Singapore
基金
英国医学研究理事会;
关键词
NEURONAL MIGRATION; WIDE SPECTRUM; MUTATIONS; BRAIN;
D O I
10.1002/ajmg.a.61444
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:576 / 578
页数:3
相关论文
共 50 条
  • [31] A recurrent de novo variant in NUSAP1 escapes nonsense-mediated decay and leads to microcephaly, epilepsy, and developmental delay
    Mo, Alisa
    Paz-Ebstein, Emuna
    Yanovsky-Dagan, Shira
    Lai, Abbe
    Mor-Shaked, Hagar
    Gilboa, Tal
    Yang, Edward
    Shao, Diane D.
    Walsh, Christopher A.
    Harel, Tamar
    CLINICAL GENETICS, 2023, 104 (01) : 73 - 80
  • [32] De novo missense variant in the KIT proto-oncogene in a child with piebaldism
    Koh, M.
    EXPERIMENTAL DERMATOLOGY, 2016, 25 : 8 - 8
  • [33] A 6.9 Mb 1qter deletion/4.4 Mb 18pter duplication in a boy with extreme microcephaly with simplified gyral pattern, vermis hypoplasia and corpus callosum agenesis
    Andrieux, Joris
    Cuvellier, Jean-Christophe
    Duban-Bedu, Benedicte
    Joriot-Chekaf, Sylvie
    Dieux-Coeslier, Anne
    Manouvrier-Hanu, Sylvie
    Delobel, Bruno
    Vallee, Louis
    EUROPEAN JOURNAL OF MEDICAL GENETICS, 2008, 51 (01) : 87 - 91
  • [34] A novel 1.4 Mb de novo microdeletion of chromosome 1q21.3 in a child with microcephaly, dysmorphic features and mental retardation
    Reddy, Sujana
    Dolzhanskaya, Natalia
    Krogh, Jacquelyn
    Velinov, Milen
    EUROPEAN JOURNAL OF MEDICAL GENETICS, 2009, 52 (06) : 443 - 445
  • [35] Functional analysis of a novel de novo variant in PPP5C associated with microcephaly, seizures, and developmental delay
    Fielder, Sara M.
    Rosenfeld, Jill A.
    Burrage, Lindsay C.
    Emrick, Lisa
    Lalani, Seema
    Attali, Ruben
    Bembenek, Joshua N.
    Hieu Hoang
    Baldridge, Dustin
    Silverman, Gary A.
    Schedl, Tim
    Pak, Stephen C.
    MOLECULAR GENETICS AND METABOLISM, 2022, 136 (01) : 65 - 73
  • [36] A de novo ATXN2L variant in a child with developmental delay and macrocephaly
    Alzahrani, Fatema
    Albatti, Turki H.
    Alkuraya, Fowzan S.
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2021, 185 (03) : 949 - 951
  • [37] A de novo inframe deletion variant in CAPZA2 tentacle domain with global developmental delay and secondary microcephaly
    Pi, Shanyu
    Mao, Xiao
    Long, Hongyu
    Wang, Hua
    CLINICAL GENETICS, 2022, 102 (04) : 355 - 356
  • [38] De Novo Mutations in the Beta-Tubulin Gene TUBB2A Cause Simplified Gyral Patterning and Infantile-Onset Epilepsy
    Cushion, Thomas D.
    Paciorkowski, Alex R.
    Pilz, Daniela T.
    Mullins, Jonathan G. L.
    Seltzer, Laurie E.
    Marion, Robert W.
    Tuttle, Emily
    Ghoneim, Dalia
    Christian, Susan L.
    Chung, Seo-Kyung
    Rees, Mark I.
    Dobyns, William B.
    AMERICAN JOURNAL OF HUMAN GENETICS, 2014, 94 (04) : 634 - 641
  • [39] A de novo synonymous variant in EFTUD2 disrupts normal splicing and causes mandibulofacial dysostosis with microcephaly: case report
    Jacob, Arthur
    Pasquier, Jennifer
    Carapito, Raphael
    Aurade, Frederic
    Molitor, Anne
    Froguel, Philippe
    Fakhro, Khalid
    Halabi, Najeeb
    Viot, Geraldine
    Bahram, Seiamak
    Rafii, Arash
    BMC MEDICAL GENETICS, 2020, 21 (01)
  • [40] De novo NUF2 variant in a novel inherited bone marrow failure syndrome including microcephaly and renal hypoplasia
    Vial, Yoann
    Lainey, Elodie
    Leblanc, Thierry
    Baudouin, Veronique
    Dourthe, Marie Emilie
    Gressens, Pierre
    Verloes, Alain
    Cave, Helene
    Drunat, Severine
    BRITISH JOURNAL OF HAEMATOLOGY, 2022, 199 (05) : 739 - 743