Aortic Valve Disease Symptoms

During ventricular systole, pressure rises in the left ventricle. When the pressure in the left ventricle rises above the pressure in the aorta, the aortic valve opens, allowing blood to exit the left ventricle into the aorta. When ventricular systole ends, pressure in the left ventricle rapidly drops. When the pressure in the left ventricle decreases, the aortic pressure forces the aortic valve to close. The closure of the aortic valve contributes the A2 component of the second heart sound.

There are two prototypical processes that can affect the aortic valve – aortic stenosis in which the valve fails to open fully, thereby obstructing blood flow out from the heart, and aortic insufficiency, also called aortic regurgitation, in which the aortic valve is incompetent and blood flows passively back to the heart in the wrong direction. These two conditions frequently co-exist. Common causes of aortic regurgitation include vasodilation of the aorta, previous rheumatic fever, infection, i.e. infective endocarditis, degeneration of the aortic valve, and Marfan’s syndrome.The most common congenital abnormality of the heart is the bicuspid aortic valve. In this condition, instead of three cusps, the aortic valve has two cusps. This condition is often undiagnosed until later in life when the person develops symptomatic aortic stenosis.

 Aortic stenosis occurs in this condition usually in patients in their 40s or 50s, an average of 10 years earlier than can occur in people with normal aortic valves. Aortic stenosis can also be caused by rheumatic fever and degenerative calcification. Aortic valve replacement is a surgical procedure in which a patient’s aortic valve is replaced by a different valve. The aortic valve can be affected by a range of diseases and require aortic valve replacement. The valve can become either leaky (regurgitant or insufficient) or stuck partially shut (stenotic). Aortic valve replacement currently requires open heart surgery. Research is being done now to develop valves that can be implanted using a catheter without open heart surgery. There are two basic types of artificial heart valve, mechanical valves and tissue valves.

 Tissue heart valves are usually made from animal tissues, either animal heart valve tissue or animal pericardial tissue. The tissue is treated to prevent rejection and to prevent calcification.There are alternatives to animal tissue valves. In some cases, a human aortic valve can be implanted. These are called homografts. Homograft valves are donated by patients and recovered after the patient expires. The durability of homograft valves is probably the same as for porcine tissue valves. Another procedure for aortic valve replacement is the Ross procedure (after Donald Ross) or pulmonary autograft. The Ross procedure involves going to surgery to have the aortic valve removed and replacing it with the patient’s own pulmonary valve.A pulmonary homograft (a pulmonary valve taken from a cadaver) or a valvular prothesis is then used to replace the patient’s own pulmonary valve. There are two prototypical processes that can affect the aortic valve – aortic stenosis in which the valve fails to open fully, thereby obstructing blood flow out from the heart, and aortic insufficiency, also called aortic regurgitation, in which the aortic valve is incompetent and blood flows passively back to the heart in the wrong direction. These two conditions frequently co-exist. Common causes of aortic regurgitation include vasodilation of the aorta, previous rheumatic fever, infection, i.e. infective endocarditis, degeneration of the aortic valve, and Marfan’s syndrome.


The most common congenital abnormality of the heart is the bicuspid aortic valve. In this condition, instead of three cusps, the aortic valve has two cusps. This condition is often undiagnosed until later in life when the person develops symptomatic aortic stenosis. Aortic stenosis occurs in this condition usually in patients in their 40s or 50s, an average of 10 years earlier than can occur in people with normal aortic valves. Aortic stenosis can also be caused by rheumatic fever and degenerative calcification.

Addison’s disease is an uncommon autoimmune disease, characterized by chronic and insufficient functioning of the outer layer of the adrenal gland. The adrenal glands are located atop each kidney and produce vital glucocorticoid hormones. Because of this chronic under-functioning of the adrenal glands, persons with Addison’s disease have a deficiency in the production of glucocorticoid hormones. Glucocorticoid hormones are involved in how the body utilizes and stores carbohydrates, protein, fat and blood sugar.

The adrenal gland also plays a role in the immune response. A deficiency in glucocorticoid hormones causes an increase in the release of sodium and a decreased release of potassium in the urine, sweat, saliva, stomach and intestines. These changes can cause low blood pressure and increased water excretion that can in some cases lead to severe dehydration.

Although there are many underlying factors in the development of adrenal insufficiencies, including destruction of the adrenal cortex due to diseases such as tuberculosis, the growth of tumors, non-autoimmune diseases amyloidosis and adrenoleukodystrophy, and atrophy of the gland due to prolonged use of cortical steroids used in the treatment of other conditions and illnesses, most cases of Addison’s disease are thought to be autoimmune in nature.

Agammaglobulinemia is an immune disorder related to antibody deficiency (hypogammaglobulinemia) and is manifested in a variety of immune deficiency disorders in which the immune system is compromised. This group of immune deficiencies may be the consequence of an inherited condition, an impaired immune system from known or unknown cause, a relation to autoimmune diseases, or a malignancy.

Immunoglobulin deficiencies may be referred to by many different names, as there are several variables within the separate but related immune disorders; and there are also many subgroups. Antibody deficiency, immunoglobulin deficiency, and gamma globulin deficiency are all synonyms for hypogammaglobulinemia.

Alopecia areata is an autoimmune disorder which is characterized by hair loss. Alopecia areata is found equally in both men and women. The disease can occur at any age, including childhood.


The hair loss may result in round bald patches on the scalp (alopecia areata) or involve the loss of all facial and scalp hair (alopecia totalis). The loss of all body hair is called alopecia universalis. Alopecia postpartum is characterized by loss of significant hair following pregnancy and is usually temporary. When a patient is diagnosed with alopecia, the first question is usually about whether or not the hair will regrow. The answer is usually vague as each case is different. Regrowth of hair may occur in some patients; and in other, the hair loss is permanent.