Angina, also known as ischemic chest pain, is a result of a deficient flow of blood to the heart. It can be a symptom of coronary artery disease. Patients describe this pain as recurrent or sudden squeezing, pressure, heaviness and tightness in the chest. A primary cause could be fatty substances building up in the arteries supplying blood to the heart. Cure/medication for Angina A healthy fusion of behavior  Read More

Autosomal dominant long QT syndrome is caused by abnormalities of the heart’s electrical conduction system. LQTS occurs if there is any defect in the ion channels, causing a delay in the time it takes for the electrical system to recharge after each heartbeat.Treatment is aimed at preventing symptoms such as syncope or cardiac arrest.For most individuals affected by Autosomal dominant long QT syndrome, the tr  Read More

There are various symptoms of the cantrell-haller-ravich syndrome. Some of them are mentioned below.The symptoms depend from person to person. While some infants can have only minor defects with an incomplete expression of the disorder, on the other hand, some infants can have life-endangering complications too. The chances of occurrence of cantrell-haller-ravich syndrome are at the time of birth with ectopia cordi  Read More

Deafness functional heart disease can impair the cardiovascular health of the patient and affect both the peripheral and central auditory systems, mostly common among older people. Heart is responsible for pumping blood and bringing oxygen to the whole body. The heart disease results in poor circulation and may reduce sufficient oxygen from reaching the brain. This can cause the nerve cells to be destroyed or damaged which causes permanent hea  Read More

Eisenmenger syndrome affects some people who have structural heart defects from birth, more specifically, a ventricular septal defect (VSD) or another shunt. A VSD is a hole in the heart that connects the left and right ventricles. It interferes with the flow of blood from the heart to the lungs, which results in abnormal blood circulation. People with this condition are born with a hole between the two pumping chambers of their hearts.  Read More

Fibrin stabilizing factor deficiency is a rare condition that can be caused by a number of different factors. The most common one is genetic, but environmental factors like smoking can also contribute to the development of the condition.There are some risk factors for developing fibrin stabilizing factor deficiency, including:Genetic factors: If you have a family history of FSF deficiency and/or a close relative  Read More

Fiedler disease is a rare genetic disorder that causes the immune system to attack healthy skin cells. The disease is most common in people of European descent, but it can be found in people of all races and ethnicities.The risk factors for Fiedler disease are not well understood, but researchers believe that there may be some things that make you more likely to develop the disease. These include:Age: Children y  Read More

There is no cure for Ormond's disease/Idiopathic retroperitoneal fibrosis, but there are medications that may help manage the symptoms. Ormond's disease is an autoimmune disorder that causes inflammation of the muscles and joints. It can affect any muscle group in your body but most commonly affects the shoulders and hips. The most common symptom is pain, although you may experience weakness or stiffness as well  Read More

Romano Ward syndrome is a type of upper motor neuron disease that causes weakness and abnormal reflexes in the arms and legs. It can be caused by trauma to the neck or spinal cord, or it may be congenital (present at birth). The most common risk factors for Romano Ward syndrome include:Age: People who are over 50 years old are more likely to have Romano Ward syndrome than younger people.Sex: Women  Read More

Sakati-nyhan syndrome is a rare genetic disorder that can cause a variety of complications. It is an autosomal recessive disorder, which means that it happens when you inherit two copies of the gene that causes sakati-nyhan syndrome from both of your parents.The disease is caused by mutations in the HEXA gene on chromosome 19. •The HEXA gene produces a protein called beta-hexosaminidase A (HEXA).  Read More

Sneddon syndrome is a rare, progressive blood vessel disease. Specifically, arteries transports pure blood away from the heart and into the body. It is largely characterized by net-like patterns of discoloration on the skin (livedo reticularis) and neurological problems caused by artery obstructions. It usually affects older adults, and the clinical manifestations starts with old age. Individual differences in symptoms and sev  Read More

There is no cure for takayasu disease (takayasu arteritis). However, a comprehensive treatment plan can be followed to improve the symptoms, reduce inflammation and prevent irreversible damage to artery walls. Takayasu disease or Takayasu Arteritis (TAK) is a type of vasculitis, a rare familial disorder characterized by inflammation of blood vessels. The condition affects the aorta and its branches, which resist the flow of bl  Read More

The Heart and Vascular disease demand the patient to induce in their lives changes such as eating healthy, exercising regularly, and not smoking. However, certain medications or surgeries help doctors deal with the heart and vascular disease to a great extent. Medications- Medicines often provided by the doctors to treat heart and vascular diseases include- Cholesterol Drugs- Medicines can help reduce cholesterol l  Read More