Venous thrombosis and ischemic brain stroke in type 2 diabetes: Etiological role of a heterozygous mutation of factor V Leiden and a polymorphism C/T of MTHFR gene

被引:0
|
作者
Boudaoud, K. [1 ]
Sifi, K. [2 ]
Abbadi, N. [3 ]
Hannachi, S. [3 ]
机构
[1] Fac Med, Serv Endocrinol Diabetol, Constantine, Algeria
[2] Fac Med, Serv Biochim, Unite Genet, Constantine, Algeria
[3] Fac Med, Biochim Lab, Unite Genet, Constantine, Algeria
关键词
D O I
10.1016/S1262-3636(10)70361-X
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
引用
收藏
页码:A89 / A89
页数:1
相关论文
共 50 条
  • [1] Neonatal renal vein thrombosis in a heterozygous carrier of both factor V Leiden and the MTHFR gene mutation
    Wannes, S.
    Soua, H.
    Ghanmi, S.
    Braham, H.
    Hassine, M.
    Hamza, H. A.
    Ben Hamouda, H.
    Sfar, M. -T.
    ARCHIVES DE PEDIATRIE, 2012, 19 (04): : 419 - 421
  • [2] Evaluation Of Factor V Leiden, Prothrombin Mutations and The Homozygous mutation 677T In The MTHFR Gene In Patients With Venous Thrombosis
    Pizzuti, Michele
    Santagostino, Alberto
    Rizzo, Maria Antonietta
    Dragonetti, Daniela
    Pietrafesa, Maria Grazia
    Attolico, Immacolata
    Amendola, Angela
    Filardi, Nunzio
    Cimminiello, Michele
    Matturro, Angela
    Vertone, Domenico
    Nuccorini, Roberta
    Pascale, Sara Pasquina
    Coluzzi, Sabrina
    BLOOD, 2013, 122 (21)
  • [3] Glanzmann Thrombasthenia in a Newborn with Heterozygous Factor V Leiden and Heterozygous MTHFR C677T Gene Mutations
    Gultekin, Nazli Dilay
    Yilmaz, Fatma Hilal
    Tokgoz, Huseyin
    Tarakci, Nuriye
    Caliskan, Umran
    INDIAN PEDIATRICS, 2019, 56 (02) : 143 - 144
  • [4] Glanzmann Thrombasthenia in a Newborn with Heterozygous Factor V Leiden and Heterozygous MTHFR C677T Gene Mutations
    Nazli Dilay Gultekin
    Fatma Hilal Yilmaz
    Huseyin Tokgoz
    Nuriye Tarakci
    Umran Caliskan
    Indian Pediatrics, 2019, 56 : 143 - 144
  • [5] Homozygous C->T mutation in the methylene tetrahydrofolate reductase (MTHFR) gene does ndt increase the risk for venous thrombosis in patients with the factor V Leiden mutation.
    Rintelen, C
    Pabinger, I
    Lechner, K
    Eichinger, S
    Kyrle, PA
    Mannhalter, C
    BLOOD, 1996, 88 (10) : 3007 - 3007
  • [6] Renal transplantation experience in a patient with factor V Leiden homozygous, MTHFR C677T heterozygous, and PAI heterozygous mutation
    Gulhan, Bora
    Tavil, Betul
    Gumruk, Fatma
    Aki, Tuncay F.
    Topaloglu, Rezan
    PEDIATRIC TRANSPLANTATION, 2015, 19 (05) : E126 - E129
  • [7] Arterial thrombosis resulting in amputation in a child with poorly controlled type 1 diabetes and heterozygous Factor V Leiden mutation
    Haller, Michael J.
    Valladares, Angelina
    Rosenbloom, Arlan L.
    PEDIATRIC DIABETES, 2006, 7 (04) : 229 - 231
  • [8] Unilateral Renal Vein Thrombosis and Adrenal Hemorrhage in A Newborn with Homozygous Factor V Leiden and Heterozygous Of MTHFR-677T, MTHFR-1298C Gene Mutations
    Gonca Sandal
    Elvan Arıkan
    Ayça Esra Kuybulu
    Ahmet Rifat Ormecı
    Indian Journal of Hematology and Blood Transfusion, 2014, 30 : 294 - 298
  • [9] Unilateral Renal Vein Thrombosis and Adrenal Hemorrhage in A Newborn with Homozygous Factor V Leiden and Heterozygous Of MTHFR-677T, MTHFR-1298C Gene Mutations
    Sandal, Gonca
    Arikan, Elvan
    Kuybulu, Ayca Esra
    Ormeci, Ahmet Rifat
    INDIAN JOURNAL OF HEMATOLOGY AND BLOOD TRANSFUSION, 2014, 30 : S294 - S298
  • [10] Deep venous thrombosis of the lower extremity in a 16-year-old girl with homozygous MTHFR- and heterozygous factor V Leiden-mutation
    Roschitz, B
    Muntean, W
    Mannhalter, C
    Koestenberger, M
    33RD HEMOPHILIA SYMPOSIUM: HAMBURG 2002, 2004, : 176 - 178