Novel frameshift variant in the PCNT gene associated with Microcephalic Osteodysplastic Primordial Dwarfism (MOPD) Type II and small kidneys

被引:0
|
作者
D. Hettiarachchi
S. M. V. Subasinghe
G. G. Anandagoda
Hetalkumar Panchal
P. S. Lai
V. H. W. Dissanayake
机构
[1] University of Colombo,Department of Anatomy, Genetics and Biomedical Informatics, Faculty of Medicine
[2] Lady Ridgeway Hospital for Children,Post Graduate Department of Bioscience
[3] Sardar Patel University,Department of Paediatrics, Yong Loo Lin School of Medicine
[4] National University of Singapore,undefined
来源
关键词
D O I
暂无
中图分类号
学科分类号
摘要
引用
收藏
相关论文
共 50 条
  • [1] Novel frameshift variant in the PCNT gene associated with Microcephalic Osteodysplastic Primordial Dwarfism (MOPD) Type II and small kidneys
    Hettiarachchi, D.
    Subasinghe, S. M., V
    Anandagoda, G. G.
    Panchal, Hetalkumar
    Lai, P. S.
    Dissanayake, V. H. W.
    BMC MEDICAL GENOMICS, 2022, 15 (01)
  • [2] Novel mutation in patients with microcephalic osteodysplastic primordial dwarfism type II (MOPD II)
    Gharehdaghi, Elika Esmaeilzadeh
    Smiley, Elina
    Zakeri, Sina
    Tale, Ali
    Klashami, Zeynab Nickhah
    Sedghi, Maryam
    Naghshband, Zeinab
    Amoli, Mahsa M.
    METABOLIC BRAIN DISEASE, 2024, 40 (01)
  • [3] A novel homozygous mutation of the PCNT gene in a Chinese patient with microcephalic osteodysplastic primordial dwarfism type II
    Liu, Haifeng
    Tao, Na
    Wang, Yan
    Yang, Yang
    He, Xiaoli
    Zhang, Yu
    Zhou, Yuantao
    Liu, Xiaoning
    Feng, Xingxing
    Sun, Meiyuan
    Xu, Fang
    Su, Yanfang
    Li, Li
    MOLECULAR GENETICS & GENOMIC MEDICINE, 2021, 9 (09):
  • [4] Molecular analysis of pericentrin gene (PCNT) in a series of 24 Seckel/microcephalic osteodysplastic primordial dwarfism type II (MOPD II) families
    Willems, M.
    Genevieve, D.
    Borck, G.
    Baumann, C.
    Baujat, G.
    Bieth, E.
    Edery, P.
    Farra, C.
    Gerard, M.
    Heron, D.
    Leheup, B.
    Le Merrer, M.
    Lyonnet, S.
    Martin-Coignard, D.
    Mathieu, M.
    Thauvin-Robinet, C.
    Verloes, A.
    Colleaux, L.
    Munnich, A.
    Cormier-Daire, V.
    JOURNAL OF MEDICAL GENETICS, 2010, 47 (12) : 797 - 802
  • [5] Microcephalic osteodysplastic primordial dwarfism type II in four Indian children with PCNT variants
    Singh, Amit
    Garg, Mahak
    Shariq, Mohammed
    Khetarpal, Preeti
    Panigrahi, Inusha
    EGYPTIAN JOURNAL OF MEDICAL HUMAN GENETICS, 2025, 26 (01)
  • [6] Identification of three novel mutations in PCNT in vietnamese patients with microcephalic osteodysplastic primordial dwarfism type II
    Nguyen, Thu Hien
    Nguyen, Ngoc-Lan
    Vu, Chi Dung
    Ngoc, Can Thi Bich
    Nguyen, Ngoc Khanh
    Nguyen, Huy Hoang
    GENES & GENOMICS, 2021, 43 (02) : 115 - 121
  • [7] Identification of three novel mutations in PCNT in vietnamese patients with microcephalic osteodysplastic primordial dwarfism type II
    Thu Hien Nguyen
    Ngoc-Lan Nguyen
    Chi Dung Vu
    Can Thi Bich Ngoc
    Ngoc Khanh Nguyen
    Huy Hoang Nguyen
    Genes & Genomics, 2021, 43 : 115 - 121
  • [8] A microcephalic osteodysplastic primordial dwarfism type 2 case with a homozygous novel mutation in PCNT
    Kabayegit, Z. Manav
    Can, E.
    Yuzbasi, B. Kipcak
    Altan, M.
    Jackson, A.
    Bozkurt, G.
    Tosun, A.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 : 365 - 365
  • [9] Novel biallelic PCNT deletion causing microcephalic osteodysplastic primordial dwarfism type II with congenital heart defect
    Meng, Lanlan
    Tu, Chaofeng
    Lu, Guangxiu
    Lin, Ge
    Tan, Yueqiu
    SCIENCE CHINA-LIFE SCIENCES, 2019, 62 (01) : 144 - 147
  • [10] Majewski Osteodysplastic Primordial Dwarfism Type II (MOPD II) Syndrome Previously Diagnosed as Seckel Syndrome: Report of a Novel Mutation of the PCNT Gene
    Piane, Maria
    Della Monica, Matteo
    Piatelli, Gianluca
    Lulli, Patrizia
    Lonardo, Fortunato
    Chessa, Luciana
    Scarano, Gioacchino
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2009, 149A (11) : 2452 - 2456