A case of atypical Kabuki syndrome arising from a novel missense variant in HNRNPK

被引:11
|
作者
Miyake, N. [1 ]
Inaba, M. [2 ]
Mizuno, S. [2 ]
Shiina, M. [3 ]
Imagawa, E. [1 ]
Miyatake, S. [1 ]
Nakashima, M. [1 ]
Mizuguchi, T. [1 ]
Takata, A. [1 ]
Ogata, K. [3 ]
Matsumoto, N. [1 ]
机构
[1] Yokohama City Univ, Dept Human Genet, Grad Sch Med, Yokohama, Kanagawa, Japan
[2] Cent Hosp Kasugai, Dept Pediat, Aichi Human Serv Ctr, Kasugai, Aichi, Japan
[3] Yokohama City Univ, Dept Biochem, Grad Sch Med, Yokohama, Kanagawa, Japan
基金
日本科学技术振兴机构;
关键词
D O I
10.1111/cge.13023
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:554 / 555
页数:2
相关论文
共 50 条
  • [1] A case of cockayne syndrome: a novel homozygous missense variant
    Kandemir, N.
    Karaduman, N. K.
    Arslan, S. B.
    Baysal, K.
    Dundar, M.
    JOURNAL OF BIOTECHNOLOGY, 2019, 305 : S88 - S88
  • [2] Au-Kline syndrome due to a de novo missense variant in HNRNPK
    Fauth, C.
    Albrecht, U.
    Maurer, E.
    Zschocke, J.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2020, 28 (SUPPL 1) : 905 - 905
  • [3] Case Report: Exome and RNA Sequencing Identify a Novel de novo Missense Variant in HNRNPK in a Chinese Patient With Au-Kline Syndrome
    Pan, Xin
    Liu, Sihan
    Liu, Li
    Zhang, Xu
    Yao, Hong
    Tan, Bo
    FRONTIERS IN GENETICS, 2022, 13
  • [4] An Atypical Case with Chronic Granulomatous Disease and Kabuki Syndrome
    Koker, Mustafa Yavuz
    Ture, Zeynep
    Koker, Nezihe
    Metan, Gokhan
    ERCIYES MEDICAL JOURNAL, 2020, 42 (02) : 229 - 232
  • [5] Novel missense WFS1 variant causing autosomal dominant atypical Wolfram syndrome
    Mair, Hailey
    Fowler, Nicholas
    Papatzanaki, Maria E.
    Sudhakar, Padmaja
    Maldonado, Ramiro S.
    OPHTHALMIC GENETICS, 2022, 43 (04) : 567 - 572
  • [6] A Novel Intronic KMT2D Variant as a Cause of Kabuki Syndrome: A Case Report
    Aristizabal, Erica
    Diaz-Ordonez, Lorena
    Candelo, Estephania
    Pachajoa, Harry
    APPLICATION OF CLINICAL GENETICS, 2021, 14 : 409 - 416
  • [7] An atypical case of early-onset dystonia with a novel missense variant in KMT2B
    Zhou, Xin-Yue
    Wu, Jian-Jun
    Sun, Yi-Min
    PARKINSONISM & RELATED DISORDERS, 2019, 63 : 224 - 226
  • [8] Novel missense mutation of the KMT2D gene in a girl with Kabuki syndrome
    Riedel, S.
    Linne, M.
    Eichhorn, B.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2020, 28 (SUPPL 1) : 347 - 347
  • [9] Clinical spectrum of Kabuki-like syndrome caused by HNRNPK haploinsufficiency. Case report and literature review
    Dentici, M.
    Barresi, S.
    Niceta, M.
    Pantaleoni, F.
    Pizzi, S.
    Dallapiccola, B.
    Tartaglia, M.
    Digilio, M.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2018, 26 : 477 - 477
  • [10] Prenatal diagnosis of auriculocondylar syndrome with a novel missense variant of GNAI3: a case report
    Xiaoliang Liu
    Wei Sun
    Jun Wang
    Guoming Chu
    Rong He
    Bijun Zhang
    Yanyan Zhao
    BMC Pregnancy and Childbirth, 21