Isolated central nervous system hemophagocytic lymphohistiocytosis caused by novel UNC13D mutation

被引：1
|
作者：
Henry, Meret [1 ,2 ,7 ]
Altinok, Deniz [3 ]
Williams, Mitchel T. T. [1 ,4 ]
Savasan, Sureyya [1 ,2 ]
Marupudi, Neena I. I. [5 ,6 ]
机构：
[1] Cent Michigan Univ, Dept Pediat, Mount Pleasant, MI USA
[2] Childrens Hosp Michigan, Div Hematol Oncol Stem Cell Transplantat, Detroit, MI USA
[3] Childrens Hosp Michigan, Dept Radiol, Detroit, MI USA
[4] Childrens Hosp Michigan, Div Child Neurol, Detroit, MI USA
[5] Wayne State Univ, Sch Med, Dept Neurosurg, Detroit, MI USA
[6] Childrens Hosp Michigan, Div Pediat Neurosurg, Detroit, MI USA
[7] Cent Michigan Univ, Childrens Hosp Michigan, Dept Pediat, 3901 Beaubien, Mount Pleasant, MI 48859 USA
来源：
PEDIATRIC BLOOD & CANCER | 2023年 / 70卷 / 09期
关键词：
D O I：
10.1002/pbc.30482
中图分类号：
R73 [肿瘤学];
学科分类号：
100214 ;
摘要：
引用
收藏
页数：3
相关论文
共 50 条
  • [1] Familial Hemophagocytic Lymphohistiocytosis due to Mutation of UNC13D Gene
    Prabhas Prasun Giri
    Nirmoy Biswas
    Swati Chakravarty
    [J]. Indian Journal of Hematology and Blood Transfusion, 2016, 32 : 344 - 346
  • [2] UNC13D mutation presenting as fulminant familial hemophagocytic lymphohistiocytosis
    Liao, Chun-Hua
    Lee, Ni-Chung
    Jou, Shiann-Tarng
    Chiang, Bor-Luen
    Yu, Hsin-Hui
    [J]. JOURNAL OF MICROBIOLOGY IMMUNOLOGY AND INFECTION, 2020, 53 (06) : 1039 - 1041
  • [3] Familial Hemophagocytic Lymphohistiocytosis due to Mutation of UNC13D Gene
    Giri, Prabhas Prasun
    Biswas, Nirmoy
    Chakravarty, Swati
    [J]. INDIAN JOURNAL OF HEMATOLOGY AND BLOOD TRANSFUSION, 2016, 32 : S344 - S346
  • [4] Gene Therapy for Hemophagocytic Lymphohistiocytosis (HLH) Caused by Mutations in UNC13D
    Takushi, Sarah
    [J]. MOLECULAR THERAPY, 2019, 27 (04) : 398 - 399
  • [5] Familial Hemophagocytic Lymphohistiocytosis secondary to UNC13D mutation: a report of two cases
    Payman Sadeghi
    Golnaz Ghazizadeh Esslami
    Hassan Rokni-Zadeh
    Majid Changi-Ashtiani
    Reihaneh Mohsenipour
    [J]. BMC Pediatrics, 22
  • [6] Familial Hemophagocytic Lymphohistiocytosis secondary to UNC13D mutation: a report of two cases
    Sadeghi, Payman
    Esslami, Golnaz Ghazizadeh
    Rokni-Zadeh, Hassan
    Changi-Ashtiani, Majid
    Mohsenipour, Reihaneh
    [J]. BMC PEDIATRICS, 2022, 22 (01)
  • [7] Identification of a novel nonsense mutation in the UNC13D gene from a patient with hemophagocytic lymphohistiocytosis: a case report
    Hu, Xijiang
    Liu, Dongling
    Jiang, Xiwen
    Gao, Bo
    Chen, Changying
    [J]. BMC MEDICAL GENETICS, 2018, 19
  • [8] Novel Mutations in the UNC13D Gene Carried by a Chinese Neonate with Hemophagocytic Lymphohistiocytosis
    Chen, Yuanyuan
    Wang, Zhujun
    Cheng, Yuping
    Tang, Yongmin
    [J]. YONSEI MEDICAL JOURNAL, 2013, 54 (04) : 1053 - 1057
  • [9] NOVEL MUTATIONS IN THE UNC13D GENE CARRIED BY A CHINESE NEONATE WITH HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS
    Tang, Y.
    Chen, Y.
    Wang, Z.
    Cheng, Y.
    [J]. PEDIATRIC BLOOD & CANCER, 2013, 60 : 214 - 214
  • [10] Hemophagocytic lymphohistiocytosis with UNC13D mutation triggered by parvovirus B19 infection
    Elorza, Izaskun
    Diaz de Heredia, Cristina
    Luis Dapena, Jose
    Olive, Teresa
    Vizmanos, Dominique
    Sanchez de Toledo, Jose
    [J]. PEDIATRIC BLOOD & CANCER, 2007, 49 (04) : 586 - 586
12345