نتایج جستجو برای: Hypertrophic cardiomyopathy

تعداد نتایج: 46655  

ژورنال: بیهوشی و درد 2015
اسماعیلی, وحید, امری مله, پرویز, یزدانی, شهلا,

Epidural anesthesia for cesarean section in a patient with Hypertrophic Cardiomyopathy Aim and Background: The pathophysiologic changes of Hypertrophic Cardiomyopathy is complex and the physiologic changes of pregnancy and anesthesia for cesarean section have a great effect in the hemodynamic and it can even lead to maternal death. We report a 21-year pregnant woman with HCM who were candi...

Journal: :the journal of tehran university heart center 0
sirus darabian alireza amirzadegan hakimeh sadeghian saeed sadeghian maria raissi dehkordi hamidreza goodarzynejad

background: muscle fibers overlying the intramyocardial segment of an epicardial coronary artery are termed myocardial bridge (mb). the aim of this study was to analyze the mid-term outcome of mb and to examine its possible association with angiographic findings and concomitant cardiac pathologies such as hypertrophic cardiomyopathy (hcm).   methods: from a total of 3218 patients admitted for c...

Journal: :archives of cardiovascular imaging 0
pilar egea-serrano cardiology. hospital general universitario rafael mendez, lorca, spain; cardiology. hospital general universitario rafael mendez, lorca, spain. tel: +34-968445755 ivan keituqwa intensive care unit, hospital general universitario rafael mendez, lorca, spain anai pelaez hospital general universitario rafael mendez, lorca, spain juan r gimeno cardiology. hospital clinico virgen de la arrixaca, lorca, spain

conclusions in the setting of acute left ventricular function depression in hocm, a comprehensive differential diagnosis should be established. treatment should be based on hemodynamic changes. after recovery, the prognosis is related to hocm. case presentation we present a unique case where tks occurred in a middle-aged male patient with hypertrophic obstructive cardiomyopathy (hocm) without a...

ALI ANDON PETROSSIANS, MOHAMMAD J. HASHEMI,

A 40 year old male, a known case of hypertrophic cardiomyopathy, was admitted for catheterization. At catheterization and angiography, septum was hypertrophied to about 5cm and diffuse coronary artery aneurysm was revealed. We found no previous report of coronary artery aneurysm in hypertrophic cardiomyopathy.

Journal: :the journal of tehran university heart center 0
ali hosseinsabet tehran heart center, tehran university of medical sciences, tehran, iran.

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Journal: :iranian journal of public health 0
hoorieh saghafi majid haghjoo sima sabbagh niloofar samiee farve vakilian mohammad taghi salehi omran

background: familial hypertrophic cardiomyopathy (hcm) is caused by mutations in genes encoding cardiac sarcomere proteins. nowadays genetic testing of hcm plays an important role in clinical practice by contributing to the diagnosis, prognosis, and screening of high-risk individuals. the aim of this study was developing a reliable testing strategy for hcm based on linkage analysis and appropri...

Journal: :medical journal of islamic republic of iran 0
mohammad j. hashemi from the cardiovascular research center, shahid rajaii hospital, iran university a/medical sciences, ali andon petrossians

a 40 year old male, a known case of hypertrophic cardiomyopathy, was admitted for catheterization. at catheterization and angiography, septum was hypertrophied to about 5cm and diffuse coronary artery aneurysm was revealed. we found no previous report of coronary artery aneurysm in hypertrophic cardiomyopathy.

Journal: :archives of cardiovascular imaging 0
salahuddin siddiqui internal medicine, allegheny health network medical education consortium, pittsburgh, pa 15212, usa; internal medicine, allegheny health network medical education consortium, pittsburgh, pa 15212, usa. tel: +1-(412)359-3751 khalid j manzar st joseph hospital, 1001 st joseph ln, london, , ky 40741, usa

Hypertrophic cardiomyopathy (HCM) is the most common genetic cardiovascular disease, which is caused by a multitude of mutations in genes encoding proteins of the cardiac sarcomere (1). Apical hypertrophic cardiomyopathy (AHCM) is an uncommon type of HCM. The sudden cardiac death is less likely to occur in the patients inflicted with AHCM (2). Herein, we presented the case of a 29-year-old man ...

Journal: :archives of cardiovascular imaging 0
ikram kammoun department of cardiology, ariana hospital, tunis, tunisia; department of cardiology, ariana hospital, tunis, tunisia. tel: +216-98644048 lemone houchinne department of cardiology, ariana hospital, tunis, tunisia sonia marrakchi department of cardiology, ariana hospital, tunis, tunisia wael ben amara department of cardiology, ariana hospital, tunis, tunisia zied ibn elhaj department of cardiology, ariana hospital, tunis, tunisia souha mokrani department of cardiology, ariana hospital, tunis, tunisia

conclusions according to our multimodality imaging approach, hypertrophic cardiomyopathy was the most probable diagnosis. case presentation we describe a 73-year-old woman referred to us for consultation because of a giant negative t wave on her electrocardiography. echocardiography revealed diffuse severe hypertrophy associated with hypertrophied anterolateral papillary muscles with a bifid he...

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