MonoMAC syndrome in a patient with a GATA2 mutation: Case report

被引：0
|
作者：
Farrill, O. P. M. [1 ]
Herrera, D. A. [1 ]
Vargas, F. R. [1 ]
Berron, L. [1 ]
Segura, N. H. [1 ]
机构：
[1] Ctr Med Nacl Siglo XXI, Mexican Inst Social Secur Allergy & Clin Immunol, Hosp Especialidades, Mexico City, DF, Mexico
来源：
ALLERGY | 2020年 / 75卷
关键词：
D O I：
暂无
中图分类号：
R392 [医学免疫学];
学科分类号：
100102 ;
摘要：
1524
引用
收藏
页码：189 / 189
页数：1
相关论文
共 50 条
  • [21] GATA2 mutation with recurrent haemophagocytic lymphohistiocytosis and panniculitis: a case report
    Sun, Luxi
    Xu, Na
    Shen, Min
    Wang, Rongrong
    Sun, Yang
    Zhuang, Junling
    Zhao, Yan
    Zeng, Xuejun
    Zhang, Xue
    RHEUMATOLOGY, 2021, 60 (07) : E229 - E231
  • [22] GATA2 haploinsufficiency caused by mutations in a conserved intronic element leads to MonoMAC syndrome
    Hsu, Amy P.
    Johnson, Kirby D.
    Falcone, E. Liana
    Sanalkumar, Rajendran
    Sanchez, Lauren
    Hickstein, Dennis D.
    Cuellar-Rodriguez, Jennifer
    Lemieux, Jacob E.
    Zerbe, Christa S.
    Bresnick, Emery H.
    Holland, Steven M.
    BLOOD, 2013, 121 (19) : 3830 - 3837
  • [23] A patient with a germline GATA2 mutation and primary myelofibrosis
    Rutsche, Cyrill, V
    Haralambieva, Eugenia
    Lysenko, Veronika
    Balabanov, Stefan
    Theocharides, Alexandre P. A.
    BLOOD ADVANCES, 2021, 5 (03) : 791 - 795
  • [24] IDENTIFICATION OF GATA2 MUTATION IN ASYMPTOMATIC PATIENT.
    Shams, M. R.
    Kobrynski, L.
    ANNALS OF ALLERGY ASTHMA & IMMUNOLOGY, 2014, 113 (05) : A86 - A86
  • [25] Can somatic GATA2 mutation mimic germ line GATA2 mutation?
    Sekhar, Mallika
    Pocock, Rachael
    Lowe, David
    Mitchell, Christopher
    Marafioti, Teresa
    Dickinson, Rachel
    Collin, Matthew
    Lipman, Marc
    BLOOD ADVANCES, 2018, 2 (08) : 904 - 908
  • [26] Mutations in GATA2 are associated with the autosomal dominant and sporadic monocytopenia and mycobacterial infection (MonoMAC) syndrome
    Hsu, Amy P.
    Sampaio, Elizabeth P.
    Khan, Javed
    Calvo, Katherine R.
    Lemieux, Jacob E.
    Patel, Smita Y.
    Frucht, David M.
    Vinh, Donald C.
    Auth, Roger D.
    Freeman, Alexandra F.
    Olivier, Kenneth N.
    Uzel, Gulbu
    Zerbe, Christa S.
    Spalding, Christine
    Pittaluga, Stefania
    Raffeld, Mark
    Kuhns, Douglas B.
    Ding, Li
    Paulson, Michelle L.
    Marciano, Beatriz E.
    Gea-Banacloche, Juan C.
    Orange, Jordan S.
    Cuellar-Rodriguez, Jennifer
    Hickstein, Dennis D.
    Holland, Steven M.
    BLOOD, 2011, 118 (10) : 2653 - 2655
  • [27] PULMONARY ALVEOLAR PROTEINOSIS IN MYELODYSPLASTIC SYNDROME SECONDARY TO GATA-2 MUTATION (MONOMAC SYNDROME)
    Raziq, Fazal
    Usama, Muhammad
    CHEST, 2020, 158 (04) : 455A - 455A
  • [28] A RARE CASE OF EMBERGER SYNDROME CAUSED BY A DE NOVO MUTATION IN THE GATA2 GENE
    Michelini, S.
    Cardone, M.
    Agga, M. Haag O.
    Bruson, A.
    Maltese, P. E.
    Bonizzato, A.
    Bertelli, M.
    LYMPHOLOGY, 2016, 49 (01) : 15 - 20
  • [29] Infection and myelodysplasia: A case report of GATA2 deficiency in a South African patient
    Nell, Erica-Mari
    Cornellissen, Helena
    Hodkinson, Katherine
    Urban, Michael F.
    Bassa, Fatima Cassim
    Fazel, Fatima Bibi
    Wiggill, Tracey
    Irusen, Semira
    Chapanduka, Zivanai C.
    CLINICAL CASE REPORTS, 2023, 11 (03):
  • [30] MONOMAC SYNDROME - CASE REPORT
    Vasconcelos, J.
    Marques, L.
    Cleto, E.
    Barbot, J.
    Neves, E.
    Freitas, I.
    Franchini, G.
    Vasconcelos, J.
    JOURNAL OF CLINICAL IMMUNOLOGY, 2012, 32 : 210 - 211
12345