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The common symptoms of Lymphedema include swelling in the arms and legs, a heavy feeling in the arm or leg, aching in the arm or leg, infections, and hardening of the skin.
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How is lymphedema diagnosed?
In 90% of the cases, lymphedema is diagnosed through observations, measurements, and symptoms. The remaining 10% require the use of more complex diagnostic tests such as lymphoscintigraphy. Lymphoscintigraphy is a technique.
What is primary lymphedema?
Primary lymphedema occurs without any obvious cause, and is thought to be the result of an underdeveloped or inefficient lymph system. In some cases, it may be hereditary. Swelling may be present at birth of soon after - Lymphedema Congenita; can occur in before the age of 35 - Lymphedema Praecox; or develop after age 35 - Lymphedema Tarda. Primary lymphedema is more common in females and occurs more often in the lower extremities. Primary lymphedema has been estimated to occur in about one in six thousand people, more often in females than in males (Dale, 1985). Age of onset tends to be similar within families. Primary lymphedema can be present from birth (congenital lymphedema), symptoms can begin at the time of puberty (lymphedema praecox), or onset can occur in adulthood (lymphedema tarda) (Lewis and Wald, 1984). Primary lymphedema seems to be inherited in several different ways. Milroy's and Meige's Disease are two forms of primary lymphedema that tend to show swelling below the waist and are dominantly inherited in some families. Milroy's Disease (congenital lyphedema) is characterized by swelling present from around the time of birth. Meige Disease, also known as lymphedema praecox, may appear suddenly around the time of puberty (Wheeler et al., 1981). When the first signs of swelling appear after age 35, this condition is called lymphedema tarda. A recessive form of lymphedema has also been described, as well as lymphedema in association with other traits. Except for genes on the sex chromosomes, both men and women have two copies of each gene. If only one changed copy of a gene causes a condition, the condition will be inherited in what is called a dominant pattern. If an individual has a dominant condition such as Milroy's or Meige's Disease, the chance of passing the gene to a child is 1 in 2 or 50% with each pregnancy. These odds are the same as getting "heads" in a coin toss.Dominant disorders are ones that run from generation to generation or are passed along through the family. If a person has the gene for a dominant form of primary lymphedema, there is usually a 50% or 1 in 2 chance of passing that gene on to his or her children. However, not everyone with the gene for this form of lymphedema will actually develop symptoms. Therefore, even if a child does not inherit lymphedema from a parent, he or she may still have inherited the gene and pass the gene that causes lymphedema on to a child. Although we do not yet understand why this "reduced penetrance" sometimes occurs, it is more common in men. In other words, a brother would be less likely than his sister to have symptoms of lymphedema even if they both inherit the same lymphedema gene. We hope a new understanding of the genetic basis of inherited lymphedema will provide insights into its treatment and contribute to early identification of individuals at risk.
What are the common ailments of the circulatory system and their symptoms?
The most common ailment of the circulatory system is atherosclerosis, or hardening of the arteries. This condition can lead to heart attack or stroke. Sometimes there are no symptoms, but when the problem is severe it typically causes symptoms such as chest pain, shortness of breath, weakness, nausea, and sweating. The second most common circulatory disease is hypertension, or high blood pressure. High blood pressure is very often without symptoms and has been called 'the silent killer', so it is important to get regular blood pressure checks.
What is the abnormal condition of lymph?
There are number of different terms that will fit this but the most common is lymphedema.
Lymphedema Can it be hereditary?
Yes, lymphedema can be hereditary. This is also known as congenital lymphedema. For more see. www.compressionpumps.com
What are the different stages of lymphedema?
The stages of lymphedema is Stage 0 and this stage has no swelling or signs. Stage 1 is visible swelling. Stage 2 and 3, the disease changes the tissues and infections are common.
It can be caused by cancer treatments burns or trauma?
secondary lymphedema
How long is lymphedema treated?
Lymphedema is a chronic condition that requires continuing treatment.
Could you die from lymphedema?
Lymphedema can be deadly if it is not treated. It can be treated using compression pumps and compression hosiery like this:http://www.vitalitymedical.com/Catalog/Lymphedema-Pumps-1169-.html
Could you die from having lymphedema?
Lymphedema can be deadly if it is not treated. It can be treated using compression pumps and compression hosiery like this:http://www.vitalitymedical.com/Catalog/Lymphedema-Pumps-1169-.html
What are the most common symptoms of bursitis?
Pain and tenderness are common symptoms.
What are causes of lymphedema?
Primary lymphedema is an inherited condition, where the patient is born without lymph vessels and nodes. The swelling associated with primary lymphedema usually occurs during adolescence and affects the foot or calf.
