Unilateral Renal Vein Thrombosis and Adrenal Hemorrhage in A Newborn with Homozygous Factor V Leiden and Heterozygous Of MTHFR-677T, MTHFR-1298C Gene Mutations

被引：0

作者：

Gonca Sandal

Elvan Arıkan

Ayça Esra Kuybulu

Ahmet Rifat Ormecı

机构：

[1] Suleyman Demirel University Medical School,Department of Pediatrics

来源：

Indian Journal of Hematology and Blood Transfusion | 2014年 / 30卷

关键词：

Newborn; Renal vein thrombosis; Adrenal hemorrhage; Homozygous factor V Leiden mutation;

D O I：

暂无

中图分类号：

学科分类号：

摘要：

Renal vein thrombosis (RVT) occurs as an acute and life-threatening event in neonates. RVT is the most common non–catheter-related thrombosis in infancy and occurs primarily in the newborn period. Non-catheter-related abdominal thrombosis on neonates has a higher incidence of genetic prothrombotic risk factors. RVT and adrenal hemorrhage can both be encountered in the neonatal period and they may occur at the same time (Bokenkamp et al., Eur J Pediatr 159:44–8, 2000; Lau et al. Pediatrics 120:1278–84, 2007). We report a case of unilateral RVT and adrenal hemorrhage in a newborn with homozygous factor V Leiden mutation and heterozygous of the methylene tetrahydrofolate reductase (MTHFR) gene mutations.

引用

页码：294 / 298

页数：4

共 50 条

[41] Prevalence of the factor V Leiden mutation and the MTHFR C677T mutation in thrombophilic and in healthy persons
Gaustadnes, M
Larsen, TB
Ingerslev, J
Petersen, BN
Madsen, M
Bihl, K
Rudiger, N
THROMBOSIS AND HAEMOSTASIS, 1997, : P2324 - P2324
[42] FV LEIDEN, FII G20210A AND MTHFR C677T MUTATIONS IN PATIENTS WITH LOWER OR UPPER LIMB DEEP VEIN THROMBOSIS
Djordjevic, Valentina
Pruner, Iva
Rakicevic, Ljiljana
Kovac, Mirjana
Mikovic, Danijela
Miljic, Predrag
Antonijevic, Nebojsa
Radojkovic, Dragica
GENETIKA-BELGRADE, 2011, 43 (02): : 371 - 380
[43] Factor V Leiden and MTHFR C677 T polymorphisms and inflammation markers in diabetic retinopathy patients
Atefeh Rahimi
Nastaran Moridi
Seyed Mehdi Sajjadi
Egyptian Journal of Medical Human Genetics, 26 (1)
[44] PREVALENCE OF FACTOR V LEIDEN, PROTHROMBIN G20210A AND MTHFR C677T MUTATIONS IN DEEP VENOUS THROMBOSIS PATIENTS FROM WESTERN IRAN
Rahimi, Z.
Mozafari, H.
Mansouri, K.
Shahriari, A.
Aznab, M.
Rezaei, M.
Ali-Moghadam, K.
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, 2009, 94 : 666 - 666
[45] AXILLARY ARTERY THROMBOSIS IN A NEWBORN HOMOZYGOUS FOR METHYLENETETRAHYDROFOLATE REDUCTASE (A1298C) MUTATION AND HETEROZYGOUS FOR FACTOR V LEIDEN (G506A) MUTATION
Dilli, D.
Fettah, N.
Cinar, H. G.
Ozyazici, E.
Dursun, A.
Zenciroglu, A.
Okumus, N.
GENETIC COUNSELING, 2016, 27 (01): : 87 - 89
[46] 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
Boudaoud, K.
Sifi, K.
Abbadi, N.
Hannachi, S.
DIABETES & METABOLISM, 2010, 36 : A89 - A89
[47] THE ASSOCIATION BETWEEN FACTOR V LEIDEN, MTHFR C667T/A1298C POLYMORPHISMS AND PREGNANCY OUTCOMES
Vicoveanu, Petronela
Dimitriu, Daniela Cristina
Gorduza, E., V
Mitu, Ivona
Filip, Catalina
Socolov, Demetra
MEDICAL-SURGICAL JOURNAL-REVISTA MEDICO-CHIRURGICALA, 2021, 125 (04): : 563 - 569
[48] The prevalence of factor V (G1691A), MTHFR (C677T) and PT (G20210A) gene mutations in arterial thrombosis
Ozmen, Fusun
Ozmen, M. Mahir
Ozalp, Nejdet
Akar, Nejat
ULUSAL TRAVMA VE ACIL CERRAHI DERGISI-TURKISH JOURNAL OF TRAUMA & EMERGENCY SURGERY, 2009, 15 (02): : 113 - 119
[49] Rapid detection of MTHFR C677T+MTHFR A1298C and factor V Leiden plus prothrombin G20210A SNPs by 4-plexed real-time PCR
Hatcher, LI
Brumback, R
Baltaro, R
Gatalica, Z
Knezetic, J
JOURNAL OF MOLECULAR DIAGNOSTICS, 2004, 6 (04): : 417 - 417
[50] Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR C677T mutations in a Greek population of blood donors
Antoniadi, T
Hatzis, T
Kroupis, C
Economou-Petersen, E
Petersen, MB
AMERICAN JOURNAL OF HEMATOLOGY, 1999, 61 (04) : 265 - 267

← 1 2 3 4 5 →