Six novel mutations in the PRF1 gene in children with haemophagocytic lymphohistiocytosis

被引:66
|
作者
Clementi, R
zur Stadt, U
Savoldi, G
Varotto, S
Conter, V
De Fusco, C
Notarangelo, LD
Schneider, M
Klersy, C
Janka, G
Danesino, C
Aricò, M
机构
[1] Univ Pavia, I-27100 Pavia, Italy
[2] Univ Hamburg, Childrens Hosp, Dept Paediat Haematol & Oncol, Hamburg, Germany
[3] Univ Brescia, Pediat Clin, Ist Med Mol Angelo Nocivelli, I-25121 Brescia, Italy
[4] Univ Padua, Pediat Clin, I-35100 Padua, Italy
[5] Univ Milano Bicocca, Osped San Gerardo, Pediat Clin, Monza, Italy
[6] Osped Pausilipon, Naples, Italy
[7] Univ Ulm, Sect Expt Anaesthesiol, D-89069 Ulm, Germany
[8] IRCCS Policlin San Matteo, Biometry & Clin Epidemiol Serv, Pavia, Italy
[9] IRCCS Policlin San Matteo, Pediat Clin, Pavia, Italy
关键词
D O I
10.1136/jmg.38.9.643
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:643 / 646
页数:4
相关论文
共 50 条
  • [31] FREQUENCY OF PRF1, STX11 AND UNC13D MUTATIONS IN PATIENTS WITH A GENETIC DIAGNOSIS OF FAMILIAL HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS
    Entesarian, Miriam
    Meeths, Marie
    Rudd, Eva
    Nordenskjold, Magnus
    Henter, Jan-Inge
    PEDIATRIC BLOOD & CANCER, 2011, 56 (04) : 693 - 693
  • [32] Adult onset of primary hemophagocytic syndrome in subjects carrying PRF1 mutations
    Wang, Yini
    Wang, Zhao
    Chen, Hua
    Wang, Xiaolin
    ANNALS OF HEMATOLOGY, 2012, 91 (09) : 1489 - 1490
  • [33] Spectrum of Atypical Clinical Presentations in Patients With Biallelic PRF1 Missense Mutations
    Tesi, Bianca
    Chiang, Samuel C. C.
    El-Ghoneimy, Dalia
    Hussein, Ayad Ahmed
    Langenskiold, Cecilia
    Wali, Rabia
    Fadoo, Zehra
    Silva, Joao Pinho
    Lecumberri, Ramon
    Unal, Sule
    Nordenskjold, Magnus
    Bryceson, Yenan T.
    Henter, Jan-Inge
    Meeths, Marie
    PEDIATRIC BLOOD & CANCER, 2015, 62 (12) : 2094 - 2100
  • [34] Adult onset of primary hemophagocytic syndrome in subjects carrying PRF1 mutations
    Yini Wang
    Zhao Wang
    Hua Chen
    Xiaolin Wang
    Annals of Hematology, 2012, 91 : 1489 - 1490
  • [35] Familial CNS-Isolated Hemophagocytic Lymphohistiocytosis Due to a Novel PRF1 Mutation Triggered by SARS-CoV2
    Caldito, Natalia Gonzalez
    Lorenzo, Jocelyn
    Wang, Cynthia Xinzi
    ANNALS OF INDIAN ACADEMY OF NEUROLOGY, 2022, 25 (06) : 1170 - 1173
  • [36] Haemophagocytic lymphohistiocytosis complicating pembrolizumab treatment for metastatic breast cancer in a patient with the PRF1A91V gene polymorphism
    Al-Samkari, Hanny
    Snyder, Gregory D.
    Nikiforow, Sarah
    Tolaney, Sara M.
    Freedman, Rachel A.
    Losman, Julie-Aurore
    JOURNAL OF MEDICAL GENETICS, 2019, 56 (01) : 39 - 42
  • [37] Population studies of three X-linked immunodeficiency diseases and genotype-phenotype correlations of PRF1 mutations in familial hemophagocytic lymphohistiocytosis
    Zhang, K
    Lee, S
    Villanueva, J
    Kogawa, K
    Sumegi, J
    Wenstrup, R
    Filipovich, AH
    AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 73 (05) : 418 - 418
  • [38] Functional consequences of perforin gene mutations in 22 patients with familial haemophagocytic lymphohistiocytosis
    Feldmann, J
    Le Deist, F
    Ouachée-Chardin, M
    Certain, S
    Alexander, S
    Quartier, P
    Haddad, E
    Wulffraat, N
    Casanova, JL
    Blanche, S
    Fischer, A
    de Saint Basile, G
    BRITISH JOURNAL OF HAEMATOLOGY, 2002, 117 (04) : 965 - 972
  • [39] STXBP2 mutations in children with familial haemophagocytic lymphohistiocytosis type 5
    Cetica, Valentina
    Santoro, Alessandra
    Gilmour, Kimberly C.
    Sieni, Elena
    Beutel, Karin
    Pende, Daniela
    Marcenaro, Stefania
    Koch, Florian
    Grieve, Samantha
    Wheeler, Rachel
    Zhao, Fang
    zur Stadt, Udo
    Griffiths, Gillian M.
    Arico, Maurizio
    JOURNAL OF MEDICAL GENETICS, 2010, 47 (09) : 595 - 600
  • [40] Familial Hemophagocytic Lymphohistiocytosis Type 2 in a Chinese Infant with PRF1 Homozygous Mutation: a Case Report
    Ji, Qiong
    Wang, Guohua
    Xu, Wei
    CLINICAL LABORATORY, 2020, 66 (07) : 1411 - 1414