نتایج جستجو برای: hellp syndrome

تعداد نتایج: 622039  

2017
Adam E. Mikolajczyk John Renz Geraldine Diaz Lindsay Alpert John Hart Helen S. Te

A healthy, 30-year-old woman at 32 weeks gestation presented to the emergency department with sudden-onset headache and abdominal pain. On physical exam, she was hypertensive (188/69 mm Hg) and had mild tenderness to palpation in the right upper quadrant. Initial laboratory studies revealed proteinuria, aspartate aminotransferase at 730 U/L, and alanine aminotransferase at 478 U/L. She was diag...

Journal: :Nephrology Dialysis Transplantation 2023

Abstract Background and Aims HELLP (hemolysis, elevated liver enzymes, low platelets) is a severe variant of preeclampsia whose pathogenesis remains unknown but likely involves abnormal placentation, endothelial dysfunction release vasoactive substances. Complement dysregulation implicated in the atypical hemolytic uremic syndrome (aHUS) there growing evidence to support its role syndrome. Here...

Journal: :The British journal of ophthalmology 1990
S R Leff D L Yarian L Masciulli S N Green R E Baldomero

In the last trimester of an uncomplicated pregnancy a woman developed a spontaneous vitreous haemorrhage. She was later diagnosed as having HELLP syndrome, a recently described disorder comprising haemolytic anaemia, elevated liver enzymes, and a low platelet count in women with severe pre-eclampsia or eclampsia. We believe this rare complication of pregnancy to be the cause of the intraocular ...

2012
Hisako Fujimaki Toshiyuki Nakazawa Masaki Ueno Takayuki Imura Wataru Saito Naonobu Takahira Masashi Takaso

INTRODUCTION Subarachnoid hemorrhages of spinal origin are extremely rare during pregnancy. We present the case of a patient with hemolytic anemia, elevated liver enzymes and low platelet count (the so-called HELLP syndrome), a potentially life-threatening complication associated with pre-eclampsia, who presented with an idiopathic spinal subarachnoid hematoma. CASE PRESENTATION At 29 gestati...

Journal: :Thrombosis and haemostasis 2009
Attila Molvarec János Rigó Tamás Bõze Zoltán Derzsy László Cervenak Veronika Makó Tímea Gombos Miklós László Udvardy Jolán Hársfalvi Zoltán Prohászka

The activity of ADAMTS13, the von Willebrand factor (VWF) cleaving protease is low in several conditions, including HELLP (haemolysis, elevated liver enzymes, and low platelet count) syndrome. As HELLP syndrome develops in most cases on the basis of preeclampsia, our aim was to determine whether plasma ADAMTS13 activity is decreased in preeclampsia. Sixty-seven preeclamptic patients, 70 healthy...

2016
Manisha Shrivastava Nehal Shah

The thrombotic microangiopathies (TMA) are a group of common microvascular occlusive disorders characterized by thrombocytopenia, microangiopathic hemolysis and multiorgan dysfunction. The pathological features are vascular damage manifested by arteriolar and capillary thrombosis with characteristic abnormalities in the endothelium and vessel wall. Pregnancy associated TMA is a life threatening...

Journal: :Euro surveillance : bulletin Europeen sur les maladies transmissibles = European communicable disease bulletin 2013
J Clement V Vergote L Laenen M Van Ranst

To the editor: In their recent article, Macé et al. pointed appropriately to the many disturbing clinical similarities between haemorrhagic fever with renal syndrome (HFRS) due to Seoul virus (SEOV) infection – an emerging zoonosis – and two pregnancy-related pathologies affecting mainly the liver, acute fatty liver of pregnancy (AFLP) syndrome and haemolysis, elevated liver enzymes and low pla...

Ashraf Jamal , Azin Alavi , Sanaz Moosavi ,

Introduction: Hyperreactio Luteinalis (HL) is a rare benign condition in pregnancy which is characterized by bilaterally multicystic ovarian enlargement containing theca lutein cysts caused by increased production of hCG. HL is mostly associated with hydatidiform mole and multiple pregnancies. Correspondence: Azin Alavi, ...

Journal: :International Journal of Reproduction, Contraception, Obstetrics and Gynecology 2017

Journal: :Arquivos de neuro-psiquiatria 2009
Anderson Kuntz Grzesiuk Renato Melo Ademar Rodrigues Carvalho

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