A novel missense mutation of the KDM6A gene in an Albanian female patient with Kabuki type 2 syndrome

被引:0
|
作者
Babameto-Laku, Anila [1 ]
Gjikopulli, Agim [2 ]
Bushati, Aida [3 ]
机构
[1] Univ Hosp Ctr Mother Teresa, Serv Med Genet, Fac Med, Tirana, Albania
[2] Univ Hosp Ctr Mother Teresa, Serv Pediat Endocrinol, Fac Med, Tirana, Albania
[3] Univ Hosp Ctr Mother Teresa, Serv Pediat Neurol, Fac Med, Tirana, Albania
关键词
D O I
暂无
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
EP12.041
引用
收藏
页码:229 / 229
页数:1
相关论文
共 50 条
  • [31] Update of the genotype and phenotype of KMT2D and KDM6A by genetic screening of 100 patients with clinically suspected Kabuki syndrome
    Murakami, Hiroaki
    Tsurusaki, Yoshinori
    Enomoto, Keisuke
    Kuroda, Yukiko
    Yokoi, Takayuki
    Furuya, Noritaka
    Yoshihashi, Hiroshi
    Minatogawa, Mari
    Abe-Hatano, Chihiro
    Ohashi, Ikuko
    Nishimura, Naoto
    Kumaki, Tatsuro
    Enomoto, Yumi
    Naruto, Takuya
    Iwasaki, Fuminori
    Harada, Noriaki
    Ishikawa, Aki
    Kawame, Hiroshi
    Sameshima, Kiyoko
    Yamaguchi, Yu
    Kobayashi, Masahisa
    Tominaga, Makiko
    Ishikiriyama, Satoshi
    Tanaka, Toshiaki
    Suzumura, Hiroshi
    Ninomiya, Shinsuke
    Kondo, Akane
    Kaname, Tadashi
    Kosaki, Kenjiro
    Masuno, Mitsuo
    Kuroki, Yoshikazu
    Kurosawa, Kenji
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2020, 182 (10) : 2333 - 2344
  • [32] A NOVEL MUTATION IN A PRIMARY IMMUNODEFICIENCY PATIENT REVEALING KABUKI SYNDROME
    Mehta, M.
    Kobrynski, L.
    Shih, J.
    ANNALS OF ALLERGY ASTHMA & IMMUNOLOGY, 2016, 117 (05) : S86 - S86
  • [33] A novel de novo mutation involving the MLL2 gene in a Kabuki syndrome patient presenting with seizures
    Bekircan-Kurt, Can Ebru
    Simsek-Kiper, Pelin Ozlem
    Boduroglu, Koray
    Dericioglu, Nese
    TURKISH JOURNAL OF PEDIATRICS, 2016, 58 (01) : 97 - 100
  • [34] De Novo Exonic Deletion of KDM6A in a Chinese Girl with Kabuki Syndrome: A Case Report and Brief Literature Review
    Yang, Pu
    Tan, Hu
    Xia, Yan
    Yu, Qian
    Wei, Xianda
    Guo, Ruolan
    Peng, Ying
    Chen, Chen
    Li, Haoxian
    Mei, Libin
    Huang, Yanru
    Liang, Desheng
    Wu, Lingqian
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2016, 170 (06) : 1613 - 1621
  • [35] Five Novel Variants of KMT2D/KDM6A Found in Seven Chinese Patients with Kabuki syndrome and a literature review of 39 patients reported in China
    Chen, Ruimin
    Gong, Chunxiu
    Shangguan, Huakun
    Su, Chang
    Ouyang, Qian
    Cao, Bingyan
    Wang, Jian
    HORMONE RESEARCH IN PAEDIATRICS, 2019, 91 : 443 - 443
  • [36] Identification of novel mutation in KMT2D gene in a patient with Kabuki syndrome and borderline chromosomal instability
    Pietrzyk, A.
    Litwinska, Z.
    Gos, M.
    Bryskiewicz, M.
    Studniak, E.
    Dlugoszewska, M.
    Gambin, T.
    Zajaczek, S.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 : 992 - 993
  • [37] Impaired complex I assembly in a Leigh syndrome patient with a novel missense mutation in the ND6 gene
    Ugalde, C
    Triepels, RH
    Coenen, MJH
    van den Heuvel, LP
    Smeets, R
    Uusimaa, J
    Briones, P
    Campistol, J
    Majamaa, K
    Smeitink, JAM
    Nijtmans, LGJ
    ANNALS OF NEUROLOGY, 2003, 54 (05) : 665 - 669
  • [38] Cystic biliary atresia with paucity of bile ducts and gene mutation in KDM6A: a case report
    Daisuke Masui
    Suguru Fukahori
    Tatsuki Mizuochi
    Yoriko Watanabe
    Kaori Fukui
    Shinji Ishii
    Nobuyuki Saikusa
    Naoki Hashizume
    Naruki Higashidate
    Saki Sakamoto
    Aiko Takato
    Koh-ichiro Yoshiura
    Yoshiaki Tanaka
    Minoru Yagi
    Surgical Case Reports, 5
  • [39] Cystic biliary atresia with paucity of bile ducts and gene mutation in KDM6A: a case report
    Masui, Daisuke
    Fukahori, Suguru
    Mizuochi, Tatsuki
    Watanabe, Yoriko
    Fukui, Kaori
    Ishii, Shinji
    Saikusa, Nobuyuki
    Hashizume, Naoki
    Higashidate, Naruki
    Sakamoto, Saki
    Takato, Aiko
    Yoshiura, Koh-ichiro
    Tanaka, Yoshiaki
    Yagi, Minoru
    SURGICAL CASE REPORTS, 2019, 5 (01)
  • [40] Waardenburg syndrome type IIE in a Japanese patient caused by a novel missense mutation in the SOX10 gene
    Okamura, Ken
    Oiso, Naoki
    Tamiya, Gen
    Makino, Satoshi
    Tsujioka, Daishi
    Abe, Yuko
    Kawaguchi, Masakazu
    Hozumi, Yutaka
    Shimomura, Yoshikazu
    Suzuki, Tamio
    JOURNAL OF DERMATOLOGY, 2015, 42 (12): : 1211 - 1212