Genotypic and phenotypic character of Chinese neonates with congenital protein C deficiency: a case report and literature review

被引:0
|
作者
Xiaoying Li
Xiaoyan Li
Xiao Li
Yuanhua Zhuang
Lili Kang
Xiuli Ju
机构
[1] Qilu Children’s Hospital of Shandong University,
[2] People’s Hospital of Rongcheng,undefined
[3] Qilu Hospital of Shandong University,undefined
来源
关键词
Neonate; gene; Protein C; Purpura fulminans; Thrombosis;
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] Genotypic and phenotypic character of Chinese neonates with congenital protein C deficiency: a case report and literature review
    Li, Xiaoying
    Li, Xiaoyan
    Li, Xiao
    Zhuang, Yuanhua
    Kang, Lili
    Ju, Xiuli
    THROMBOSIS JOURNAL, 2019, 17 (01)
  • [2] Genotypic and phenotypic characteristics of Chinese neonates with cutaneous mastocytosis: a case report and literature review
    Li, Yanfang
    Li, Xiaoying
    Liu, Xianghong
    Kang, Lili
    Liu, Xinjie
    JOURNAL OF INTERNATIONAL MEDICAL RESEARCH, 2020, 48 (09)
  • [3] Liver transplantation for congenital protein C deficiency with initial poor graft function: a case report with literature review
    Sakamoto, Atsushi
    Ishiguro, Akira
    Fukuda, Akinari
    Sakamoto, Seisuke
    Suenobu, So-ichi
    Matsumoto, Tomoko
    Nogami, Keiji
    Ohga, Shouichi
    Kasahara, Mureo
    INTERNATIONAL JOURNAL OF HEMATOLOGY, 2021, 114 (01) : 141 - 145
  • [4] Liver transplantation for congenital protein C deficiency with initial poor graft function: a case report with literature review
    Atsushi Sakamoto
    Akira Ishiguro
    Akinari Fukuda
    Seisuke Sakamoto
    So-ichi Suenobu
    Tomoko Matsumoto
    Keiji Nogami
    Shouichi Ohga
    Mureo Kasahara
    International Journal of Hematology, 2021, 114 : 141 - 145
  • [5] Ophthalmic manifestations of congenital protein C deficiency: a case report and mini review
    Fariba Ghassemi
    Fatemeh Abdi
    Mandana Esfahani
    BMC Ophthalmology, 20
  • [6] Ophthalmic manifestations of congenital protein C deficiency: a case report and mini review
    Ghassemi, Fariba
    Abdi, Fatemeh
    Esfahani, Mandana
    BMC OPHTHALMOLOGY, 2020, 20 (01)
  • [7] Genotypic and phenotypic analysis of an oculocutaneous albinism patient: a case report and review of the literature
    Qian Ma
    Weiwei Wang
    Journal of Medical Case Reports, 18 (1)
  • [8] Genotypic and phenotypic spectrum of TRIT1 dysfunction: Case report and literature review
    Lince-Rivera, I.
    Cordoba, N. Martinez
    de la Rosa, J. S. Ortiz
    EPILEPSIA, 2024, 65 : 494 - 495
  • [9] Phenotypic and genotypic features of a pair of Chinese identical twins with congenital insensitivity to pain and anhidrosis A case report
    Li, Ningbo
    Sun, Jiaoli
    Guo, Shanna
    Liu, Yi
    Wang, Cong
    Zhu, Changmao
    Zhang, Xianwei
    MEDICINE, 2018, 97 (47)
  • [10] PLEDs in an infant with congenital protein C deficiency: A case report
    Sekiguchi, Kazuhito
    Akiyoshi, Kensuke
    Okazaki, Naho
    Yamada, Hiroshi
    Suzuki, Masayoshi
    Maeda, Tomoki
    Suenobu, So-ichi
    Izumi, Tatsuro
    Kang, Dongchon
    CLINICAL NEUROPHYSIOLOGY, 2010, 121 (05) : 800 - 801