A de novo ATXN2L variant in a child with developmental delay and macrocephaly

被引:2
|
作者
Alzahrani, Fatema [1 ]
Albatti, Turki H. [2 ]
Alkuraya, Fowzan S. [1 ,3 ]
机构
[1] King Faisal Specialist Hosp & Res Ctr, Dept Genet, Riyadh, Saudi Arabia
[2] Abdullatif Al Fozan Ctr Autism, Al Khobar, Saudi Arabia
[3] Alfaisal Univ, Coll Med, Dept Anat & Cell Biol, Riyadh, Saudi Arabia
关键词
ATAXIN-2;
D O I
10.1002/ajmg.a.62007
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:949 / 951
页数:3
相关论文
共 50 条
  • [21] First report of a de novo missense variant in SRCAP in a child with neurodevelopmental delay and musculoskeletal abnormalities
    Meyer, Zianka
    Weiss, Stefan
    Friday, Douglas
    Kummerow, Sophia
    Huening, Irina
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2024, 32 : 1058 - 1058
  • [22] A de novo variant in RAC3 causes severe global developmental delay and a middle interhemispheric variant of holoprosencephaly
    Hiraide, Takuya
    Yasui, Hikari Kaba
    Kato, Mitsuhiro
    Nakashima, Mitsuko
    Saitsu, Hirotomo
    JOURNAL OF HUMAN GENETICS, 2019, 64 (11) : 1127 - 1132
  • [23] A de novo variant in RAC3 causes severe global developmental delay and a middle interhemispheric variant of holoprosencephaly
    Takuya Hiraide
    Hikari Kaba Yasui
    Mitsuhiro Kato
    Mitsuko Nakashima
    Hirotomo Saitsu
    Journal of Human Genetics, 2019, 64 : 1127 - 1132
  • [24] A de novo marker chromosome derived from chromosome 20 in a child with global developmental delay
    Botelho, Pedro
    Souto, Marta
    Sousa, Marisa
    Sousa, Susana
    Martins, Marcia
    Moutinho, Osvaldo
    Leite, Rosario Pinto
    CHROMOSOME RESEARCH, 2011, 19 : S101 - S101
  • [25] When misleading signs lead to the correct diagnosis: familial macrocephaly and a de novo PTEN novel variant in a boy with neurodevelopmental delay.
    Graziani, Ludovico
    Piceci Sparascio, Francesci
    Bengala, Mario
    Terracciano, Allessandra
    Galasso, Cinzia
    Novelli, Antonio
    Novelli, Giuseppe
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2024, 32 : 1224 - 1224
  • [26] Deep intronic de novo germline EHMT1 variant in a patient with syndromic developmental delay
    Peters, Sophia
    Schmidt, Axel
    Bender, Tim
    Cremer, Kirsten
    Perne, Claudia
    Mangold, Elisabeth
    Raschke, Heidrun
    Heimbach, Andre
    Sivalingam, Sugirthan
    Krawitz, Peter
    Engels, Hartmut
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2023, 31 : 173 - 173
  • [27] A novel de novo TMEM63A variant in a patient with severe hypomyelination and global developmental delay
    Fukumura, Shinobu
    Hiraide, Takuya
    Yamamoto, Akiyo
    Tsuchida, Kousuke
    Aoto, Kazushi
    Nakashima, Mitsuko
    Saitsu, Hirotomo
    BRAIN & DEVELOPMENT, 2022, 44 (02): : 178 - 183
  • [28] De novo pathogenic variant in TUBB2A presenting with arthrogryposis multiplex congenita, brain abnormalities, and severe developmental delay
    Ejaz, Resham
    Lionel, Anath C.
    Blaser, Susan
    Walker, Susan
    Scherer, Stephen W.
    Babul-Hirji, Riyana
    Marshall, Christian R.
    Stavropoulos, Dimitri J.
    Chitayat, David
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2017, 173 (10) : 2725 - 2730
  • [29] De novo missense variant in GRIA2 in a patient with global developmental delay, autism spectrum disorder, and epileptic encephalopathy
    Latsko, Maeson S.
    Koboldt, Daniel C.
    Franklin, Samuel J.
    Hickey, Scott E.
    Williamson, Rachel K.
    Garner, Shannon
    Ostendorf, Adam P.
    Lee, Kristy
    White, Peter
    Wilson, Richard K.
    COLD SPRING HARBOR MOLECULAR CASE STUDIES, 2022, 8 (04):
  • [30] Exome reports A de novo GNB2 variant associated with global developmental delay, intellectual disability, and dysmorphic features
    Fukuda, Tokiko
    Hiraide, Takuya
    Yamoto, Kaori
    Nakashima, Mitsuko
    Kawai, Tomoko
    Yanagi, Kumiko
    Ogata, Tsutomu
    Saitsu, Hirotomo
    EUROPEAN JOURNAL OF MEDICAL GENETICS, 2020, 63 (04)