نتایج جستجو برای: cardiac abnormalities

تعداد نتایج: 368757  

Abdol Ali Malmasi Masood Selk Ghaffari Sarang Soroori

This case report describes several electrocardiographic findings in an 8-years old female Pomeranian dog that was referred with a history of digoxin overdose. Electrocardiographic abnormalities detected in this case could be classified as primary electrocardiographic disturbances, reflecting cardiac chamber enlargement and secondary ECG changes, attributed to digoxin toxicity. ECG manifestatio...

اسلامی, سمیرا, بابایی, احمد, نباتی, مریم, پیران, راژان,

Aneurysms of sinus of Valsalva are rare cardiac abnormalities. They are dilatations of the aortic sinuses and are classified as congenital or acquired. If located in the right coronary sinus they are usually ruptured into right heart chambers and frequently a ventricular septal defect coexists with this condition. This paper reports a 30-year-old woman with ruptured aneurysm of the right sinus ...

Danial Habibi, Fatemeh Dorreh Roghayeh Ahmadi Yazdan ghandi,

Kawasaki disease is an acute inflammatory disorder of medium-sized arteries that predominantly affects cardiac coronary arteries and children under the age of 5 years. Cardiac involvement usually happens later than 10 days after the onset of illness. Most of cardiac complications are coronary artery abnormalities (ectasia or aneurysms) and subclinical myocarditis. Clinical myocarditis (symptoma...

Journal: :Jaffna medical journal 2022

Cardiac rhythm abnormality is a common finding in patients with leptospirosis. Relative bradycardia, atrial fibrillation, flutter and ventricular premature beats are the arrhythmias seen In present case, patient presented septic shock had fibrillation. Further evaluation revealed hypokalemic acute kidney injury severe metabolic acidosis. The fibrillation reverted to sinus after correction of hy...

Background & Aims: Congenital anomaly is characterized by any anatomical defects present in a baby at birth that may cause major medical, surgical, or cosmetic consequences. the present study aimed to determine the prevalence of congenital anomalies and related factors among infants in Hamadan Fatemiyeh and Behesht hospitals in 2015.   Materials & Methods: this case series study...

Journal: :Archives of disease in childhood 1990
R M John D Hunter R H Swanton

Cardiac involvement is well recognised in most forms of the mucopolysaccharidoses but there is poor documentation of abnormalities specific to Morquio's syndrome (type IV mucopolysaccharidosis). Ten patients with the classic form or type A Morquio's syndrome with a median age of 12.5 years underwent echocardiographic assessment. Abnormalities were detected in six (60%) cases with mitral valve i...

Journal: :Functional neurology 2014
Gaby Pons van Dijk Elly van der Kooi Anthony Behin Joep Smeets Janneke Timmermans Silvère van der Maarel George Padberg Nicol Voermans Baziel van Engelen

The exact prevalence and nature of cardiac involvement in facioscapulohumeral muscular dystrophy (FSHD) is unknown. Nevertheless, the current opinion is that symptomatic cardiac disease is rare. We performed a cardiac screening [electrocardiogram (ECG) and echocardiography in the event of ECG abnormalities] in 75 genetically confirmed, ambulant FSHD patients without cardiac symptoms, with an ei...

Journal: :The American journal of emergency medicine 1995
R B Vukmir

Cardiac dysfunction is often manifested as arrhythmia, with disruption of the normal periodicity and regularity of electromechanical activity. Cardiac arrhythmias, or abnormalities of cardiac rhythm, are associated with a diverse group of conditions, including congenital, metabolic, structural, physiological, and immunological, and infectious abnormalities. Dysarrhythmia may also be classified ...

رشیدی قادر , فریبا, طالع , علی, علایی , عبدالرسول, مجتهدزاده , فریدون,

Mucopolysaccharidosis type maroteaux-lamy is a very rare hereditary disease. The disease is marked by the deficiency of the lysosomal enzyme N-Acetyl galactosamine-a-4-sulfate sulfatase (arylsulfatase B). It is inherited as an autosomal recessive trait. The most clinical manifestations are: corneal clouding, organomegaly, hernias, coarse facial features, cardiac insufficiency and skeletal abn...

Journal: :Resuscitation 2000

Electrolyte abnormalities are among the most common reasons for patients to develop cardiac arrhythmias. Of all the electrolyte abnormalities, hyperkalemia is most rapidly fatal. A high degree of clinical suspicion and aggressive treatment of underlying electrolyte abnormalities can prevent many patients from progressing to cardiac arrest.

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