Factor XIII Deficiency in Western Afghanistan due to a Novel F13A Gene Mutation

被引：1
|
作者：
Mousavi, Sayed Hamid [1 ,2 ]
Zeinali, Sirous [3 ]
Mesbah-Namin, Seyed Alireza [4 ]
Shams, Mahmood [5 ]
Dorgalaleh, Akbar [6 ]
机构：
[1] Kateb Univ, Dept Clin Biochem, Fac Med Sci, Kabul, Afghanistan
[2] ANCOSD, Kabul, Afghanistan
[3] Pasteur Inst Iran, Biotechnol Res Ctr, Iranian Mol Med Network, Tehran, Iran
[4] Tarbiat Modares Univ, Dept Clin Biochem, Fac Med Sci, Tehran, Iran
[5] Babol Univ Med Sci, Dept Lab Sci, Paramed Fac, Babol Sar, Iran
[6] Iran Univ Med Sci, Sch Allied Med, Dept Hematol & Blood Transfus, Tehran, Iran
来源：
INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY | 2020年 / 42卷 / 01期
关键词：
DIAGNOSIS;
D O I：
10.1111/ijlh.13050
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：E1 / E3
页数：3
相关论文
共 50 条
  • [41] COAGULATION FACTOR-XIII DEFICIENCY IN FINLAND - SEARCH FOR A MUTATION
    MIKKOLA, H
    SYRJALA, M
    RASI, V
    HAMALAINEN, E
    VAHTERA, E
    PELTONEN, L
    PALOTIE, A
    THROMBOSIS AND HAEMOSTASIS, 1993, 69 (06) : 1295 - 1295
  • [42] Factor XIII deficiency in two Spanish families with a novel variant in gene F13A1 detected by next-generation sequencing; symptoms and clinical management
    Andrés Moret
    Ángel Zúñiga
    Javier Marco Ayala
    Alessandro Liquori
    Ana Rosa Cid
    Saturnino Haya
    Fernando Ferrando
    Amando Blanquer
    José Cervera
    Santiago Bonanad
    Journal of Thrombosis and Thrombolysis, 2020, 50 : 686 - 688
  • [43] Factor XIII deficiency in two Spanish families with a novel variant in gene F13A1 detected by next-generation sequencing; symptoms and clinical management
    Moret, Andres
    Zuniga, Angel
    Marco Ayala, Javier
    Liquori, Alessandro
    Rosa Cid, Ana
    Haya, Saturnino
    Ferrando, Fernando
    Blanquer, Amando
    Cervera, Jose
    Bonanad, Santiago
    JOURNAL OF THROMBOSIS AND THROMBOLYSIS, 2020, 50 (03) : 686 - 688
  • [44] Structure-functional relationship of five novel missense mutations in F13A gene predicted by molecular modelling
    Biswas, A.
    Ivaskevicius, V
    Thomas, A.
    Oldenburg, J.
    JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2011, 9 : 475 - 475
  • [45] Five novel mutations in factor XIII A-subunit gene cause hereditary factor XIII deficiency in four unrelated families.
    Inbal, A
    Vysokovsky, A
    Zivelin, A
    Eskaraev, R
    Rosenberg, N
    Dardik, R
    Seligsohn, U
    BLOOD, 2002, 100 (11) : 493A - 493A
  • [46] Recurrent bleeding following rhinoplasty due to factor XIII deficiency
    Karabulut, AB
    Aydin, H
    Mezdegi, A
    Ademoglu, E
    PLASTIC AND RECONSTRUCTIVE SURGERY, 2001, 108 (03) : 806 - 807
  • [47] Posttraumatic subgaleal and orbital hematoma due to factor XIII deficiency
    Natarajan, Manikandan S.
    Prabhu, Krishna
    Braganza, Andrew
    Chacko, Ari G.
    JOURNAL OF NEUROSURGERY-PEDIATRICS, 2011, 7 (02) : 213 - 217
  • [48] Post-tonsillectomy hemorrhage due to factor XIII deficiency
    Albahkaly S.
    Alkhunaizi A.
    Makki F.
    The Egyptian Journal of Otolaryngology, 2012, 28 (3) : 278 - 280
  • [49] Hemorrhagic Acquired Factor XIII (13) Deficiency and Acquired Hemorrhaphilia 13 Revisited
    Ichinose, Akitada
    SEMINARS IN THROMBOSIS AND HEMOSTASIS, 2011, 37 (04): : 382 - 388
  • [50] Relevant bleeding diathesis due to acquired factor XIII deficiency
    Janning, M.
    Holstein, K.
    Spath, B.
    Schnabel, C.
    Bannas, P.
    Bokemeyer, C.
    Langer, F.
    HAMOSTASEOLOGIE, 2013, 33 (4A): : S50 - S54
12345