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Archive for the ‘Social Security Disability’ Category

Corticobasal Ganglionic Degeneration and Social Security Disability

Friday, June 15th, 2012

Corticobasal ganglionic degeneration is a rare progressive neurodegenerative disorder. It is characterized by atrophy of several areas of the brain and nerve cell loss. This includes the basal ganglia and the cerebral cortex.

The cortex (outer layer) of the brain is severely affected by corticobasal ganglionic degeneration. This is especially true in regard to the fronto-parietal areas of the brain. These regions of the brain are located near the center-top of the head.

However, deeper areas of the brain are also affected by corticobasal ganglionic degeneration. The basal ganglia is one of the affected regions. This is where the name “corticobasal” is derived from.

Corticobasal ganglionic degeneration is a disorder that usually advances slowly. The signs and symptoms that are produced by corticobasal ganglionic degeneration are usually the result of the combined loss of brain tissue in all of the regions of the brain that are affected.

Corticobasal ganglionic degeneration is similar in several ways to frontotemporal dementia. This is true clinically, genetically and pathologically.

Frontotemporal dementia is a broad, umbrella term for a diverse group of uncommon diseases that are a form of dementia. Frontotemporal dementia primarily involves the frontal and temporal lobes of the brain.

Dementia is a loss of brain function that is a characteristic of certain disorders. Dementia affects thinking, judgment, behavior and language.

Corticobasal ganglionic degeneration takes place most of the time when a person is between the ages of 45 and 70. Women are affected by this disorder more often than men are.

Corticobasal ganglionic degeneration is known by other names. It is also referred to as CBD, corticobasal degeneration and CBGD.

The cause of corticobasal ganglionic degeneration has not yet been discovered. At the current time, there is no strong evidence that corticobasal ganglionic degeneration is an inherited disorder. There are also no known risk factors that have been identified for corticobasal ganglionic degeneration, such as toxins or infections.

There have been studies done of brain tissue of people who have corticobasal ganglionic degeneration. These studies have revealed certain characteristic cell changes that involve a brain protein that is known as tau. These studies may be of use to researchers who are trying to find the cause or causes of corticobasal ganglionic degeneration.

Signs that you might have Corticobasal Ganglionic degeneration

The first signs and symptoms that are caused by corticobasal ganglionic degeneration  usually take place on one side (unilateral). However, as this disorder progresses, the signs and symptoms usual start to involve both sides (bilateral). Some of the possible signs and symptoms are:

  1. Ÿ  Difficulty with maintaining balance
  2. Ÿ  Movements that are clumsy, shaky or slow
  3. Ÿ  The loss of movement control
  4. Ÿ  Poor coordination
  5. Ÿ  The loss of intellectual ability
  6. Ÿ  Speech that is hesitant and halting
  7. Ÿ  Difficulty with speech that is progressive
  8. Ÿ  Impairment of visual-spatial functions and skills
  9. Ÿ  Problems with comprehending language that are progressive
  10. Ÿ  Stiffness or rigidity
  11. Ÿ  Problems with walking
  12. Ÿ  Difficulty with short-term memory, such as misplacing objects or repeating questions
  13. Ÿ  Dysphagia (problems with swallowing)
  14. Ÿ  Difficulty with muscle control, such as problems controlling the muscles of the mouth and face.
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A Primitive Neuroectodermal Tumor and Social Security

Tuesday, January 31st, 2012

Cancer is far more than a single disease. Cancer is a large group of disorders. These diseases are evidenced by cells that are invasive (they invade and destroy adjacent tissue), aggressive (they divide and grow without respect to normal limits) and sometimes metastatic (they move to other areas of the body).

There are many different forms of cancer. They are usually named by where they start in your body. For example, pancreatic cancer begins in your pancreas. Esophageal cancer originates in your esophagus. Cancer may often spread to other places in your body, but it is still called by where it started.

Cancer is also classified by the type of cell that the tumor looks like. Some examples of this are lymphoma, carcinoma, blastic tumor, sarcoma and germ cell tumor.

A primitive neuroectodermal tumor is one of a group of cancers that shares certain genetic and biochemical features and arises from the same kind of early cells as a family of cancers that are known as Ewing’s sarcoma. Ewing’s sarcoma usually originates in your bone, while a primitive neuroectodermal tumor usually begins in your soft tissue. If you have been diagnosed with a primitive neuroectodermal tumor, this may enable you to receive social security disability benefits like SSDI or SSI. A wise decision is to consult the social security attorneys at disabilitycasereview.com to find out the options that are available to you. The social security attorneys at disabilitycasereview.com are experienced in matters involving disability benefits. Go to disabilitycasereview.com, today.

In many instances, a primitive neuroectodermal tumor will develop in your central nervous system and brain. In other cases, a primitive neuroectodermal tumor may take place in areas outside of your brain, such as your chest wall, pelvis or limbs.

Fortunately, a primitive neuroectodermal tumor is rare in the United States. A primitive neuroectodermal tumor is responsible for somewhere around 25% of the brain tumors that take place in children. Around 8 out of every 1 million children are affected by a primitive neuroectodermal tumor each year in the United States. Most of the time, this tumor takes place in children or adults who are under the age of 25.

A primitive neuroectodermal tumor is brought about by cells that mutate and begin to multiply and grow out of control. However, no one has yet discovered why this starts to take place. It is believed by researchers that genetics may play a significant role is leading to this form of cancer.

There are several different signs and symptoms that may be produced by a primitive neuroectodermal tumor. Some of the possible signs and symptoms are:

  • Facial weakness
  • Memory loss
  • Problems with talking
  • A change in your vision
  • Vomiting, nausea and headaches that slowly get worse
  • Weakness in one of your arms or legs
  • Difficulty walking
  • Numbness in one of your arms or legs
  • A change in behavior or personality
  • Dizziness
  • Loss of coordination
  • Hearing loss
  • Unexplained weight gain or weight loss
  • Unusual sleepiness or change in your energy level
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Fuchs’ Corneal Dystrophy and Receiving Social Security

Monday, January 30th, 2012

Fuchs’ corneal dystrophy is a rare disease. Fuchs’ corneal dystrophy is a disorder that progresses slowly.

Fuchs’ corneal dystrophy involves the cornea of your eye. Your cornea is the transparent front surface of your eye.

Your endothelium (back surface of your cornea) will not permit an excess amount of fluid to accumulate in your cornea when your cornea is working like it ought to. Your endothelium cells start to slowly deteriorate and die when you are afflicted with Fuchs’ corneal dystrophy.

Fuchs’ is characterized by fluid accumulating in your cornea. This brings about a variety of problems with your vision that includes blindness.

Fuchs’ corneal dystrophy gets its name from the Austrian ophthalmologist, Ernst Fuchs. In 1910, he was the first person to describe this disease.

Fuchs’ corneal dystrophy is referred to in other ways. It is also known as endothelial corneal dystrophy, Fuchs’ dystrophy and endothelial dystrophy.

As has already been stated, this corneal dystrophy is a rare disorder of your eye. This disease affects only about 1% of the general population of the United States. Women are more likely to develop Fuchs’ corneal dystrophy than men are.

Only in rare instances does Fuchs’ corneal dystrophy affect the vision of people who are not in their 50s and 60s. This is true even though people who are in their 30s and 40s may show signs and symptoms of this disease. Are you experiencing signs and symptoms that may be an indication of Fuchs’ corneal dystrophy. If this is the case, this may enable you to obtain social security disability benefits like SSDI or SSI. A good decision is to get in touch with one of the social security attorneys at disabilitycasereview.com. The social security attorneys at disabilitycasereview.com are experienced when it comes to what it takes to get disability benefits.

In some instances, the thing that brings about Fuchs’ corneal dystrophy is not known. However, most of the time, this eye disorder is an inherited disease. What this means is that it is passed down to you from your parents.

The manner is which Fuchs’ corneal dystrophy is inherited is what is referred to as autosomal dominant. What this means is that if either one of your parents has the disease, you have a 50% chance of having it also.

The signs and symptoms that are produced by corneal dystrophy will affect both of your eyes in most cases. Some of the signs and symptoms that you may experience include:

  • Visual impairment, changes in your vision and distortion of your vision
  • Having difficulty with your vision at night
  • Epithelial blisters (tiny, painful blisters) that develop on the surface of your cornea as a result of excess fluid in your cornea
  • Your vision being blurred when you first wake up
  • Your vision gradually clearing through the remainder of the day
  • Seeing halos around lights (astigmatism)
  • A cloudy or hazy appearance to your cornea
  • Eye pain
  • A sensitivity to light
  • Blindness
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Pulmonic Stenosis and Receiving Social Security

Thursday, January 26th, 2012
Heart stenosis

Heart Stenosis

Your pulmonary artery is what takes blood from your heart to your lungs. When your heart beats, your right ventricle (lower right chamber of your heart) contracts and pushes blood out of your heart in to your pulmonary artery.

Located between the lower right chamber of your heart and your main pulmonary artery is a heart valve that is known as the pulmonic valve. What your pulmonic valve does is prevent blood from leaking back into your heart in between your heartbeats.

Your pulmonic valve is made up of three thin leaflets when it is normal. When your pulmonic valve is defective, the condition is known as pulmonic stenosis.

Pulmonic stenosis is characterized by the leaflets of your pulmonic valve being too thick, fused together or fewer than three. When this occurs, your pulmonic valve is too narrow. This leads to your heart being required to work harder in order to pump the right amount of blood to your body.

Pulmonic stenosis may bring about only minor or mild obstruction of your pulmonic valve. However, pulmonic stenosis can also cause obstruction that is moderate, severe or critical.

Pulmonic artery stenosis usually results from a defect that develops during the forming of an unborn baby’s heart. When a defect occurs before you are born, it is said to be congenital. This means that in most instances, pulmonic stenosis is something that you are born with. At the present time, no one knows what causes this defect in your pulmonic valve to occur. If you are afflicted with pulmonic stenosis, you may meet the requirements for receiving social security disability benefits, such as SSDI or SSI. A wise decision is to seek the counsel of one of the social security attorneys at disabilitycasereview.com. The social security attorneys at disabilitycasereview.com have a great deal of experience in matters relating to disability benefits.

There are times when having an artificial heart valve or other medical disorders may also lead to pulmonic stenosis. This is especially true of older people. These medical conditions include:

  • Rheumatic fever, which is a complication of an infection caused by streptococcus bacteria, such as strep throat or scarlet fever.
  • Carcinoid syndrome, which is a syndrome that is characterized by flushing of your skin and diarrhea. It is caused by the release of a chemical that is called serotonin. Serotonin gets released by growths in your digestive system that are referred to as carcinoid tumors.

Even though pulmonic stenosis results from birth defects most of the time, there are some risk factors that may increase your risk of developing this condition. Some of the conditions that may result in pulmonic stenosis are:

  • Rheumatic fever
  • Noonan’s syndrome
  • Carcinoid syndrome

5 signs you might have Pulmonic Stenosis

The signs and symptoms that pulmonic stenosis produces are usually determined by the extent to which your blood is obstructed as it flows from your right ventricle to your lungs. Signs and symptoms include:

  • A heart murmur
  • Shortness of breath that is more prominent during exertion
  • Fatigue
  • Chest pain
  • Fainting
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Neurogenic Thoracic Outlet Syndrome and Disability Benefits

Wednesday, January 25th, 2012

Your thoracic outlet is a part of your body above the top of your rib cage. Your thoracic outlet is located between your neck and your chest. Bodily structures that include Your esophagus, trachea and blood vessels and nerves that lead to your arm and neck region are some of the structures that pass through your thoracic outlet. Lying within your thoracic outlet are the arteries that are underneath your collar bone (subclavian artery) that take blood to your arms, a network of nerves that runs to your arms (brachial plexus), your first rib and your collar bone (clavicle).

Thoracic outlet syndrome is a term that is used for a group of disorders that develop when your blood vessels or your nerves that are in your thoracic outlet get squeezed or pressed together (compressed). Thoracic outlet syndrome is evidenced by pain and abnormal nerve sensations in your hand and/or arm, neck and shoulder.

Thoracic outlet syndrome is a disorder that may occur in anyone. However, it develops most of the time in women who are between the ages of 35 and 55.

As stated above, thoracic outlet syndrome is caused by your nerves and blood vessels in your thoracic outlet being compressed. There are several things that may lead to this happening. Some of these include:

  • Pressure that is placed on your joints as a result of obesity
  • Any repetitive activity in which you have to do the same thing again and again
  • Pressure that takes place on your joints from things like carrying an oversized bag or a backpack
  • Poor posture, such as drooping your shoulders or holding your head in a forward position
  • Inherited structural defects that are present at birth (congenital), such as a cervical rib (an extra rib above your first rib) or an abnormally tight fibrous band that connects your spine to your rib
  • Pregnancy, due to the fact that it may cause the loosening of your joints
  • A traumatic event, such as a car accident.

Neurogenic thoracic outlet syndrome is one of the basic types of this disorder. Neurogenic thoracic outlet syndrome is marked by your brachial plexus being squeezed and pressed together (compressed). Your brachial plexus is a network of nerves that runs out of your spinal cord. Your brachial plexus is in control of sensation and muscle movements in your hand, arm and shoulder.

Neurogenic thoracic outlet syndrome may cause several signs and symptoms. Some of these are:

  • Pain in your neck and shoulder
  • A weakening grip
  • Gilliatt-Sumner hand (wasting, deterioration in the fleshy base of your thumb)
  • An ache in your hand or arm
  • Tingling or numbness in your fingers.

You may be eligible for social security disability benefits like SSI or SSDI if you are experiencing signs and symptoms of neurogenic thoracic outlet syndrome. The best thing to do is to call on one of the social security attorneys at disabilitycasereview.com. The social security attorneys at disabilitycasereview.com are well versed in what it takes to get disability benefits.

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Factor V Leiden Thrombophilia and Receiving Disability

Monday, January 23rd, 2012

Factor V Leiden thrombophilia is an inherited genetic blood clotting disease. Factor V Leiden thrombophilia means that you will have an increased tendency to develop abnormal blood clots (thrombophilia). If abnormal blood clots do occur, they will form mainly in your veins.

In many instances, if you have factor V Leiden thrombophilia, you will never have abnormal blood clots take place. However, in other cases, you may see abnormal blood clots form that may bring about long-term, chronic health problems or become life-threatening. Are you one of those who is having chronic health problems because of factor V Leiden thrombophilia? If this is true, you may be able to get social security disability benefits like SSDI or SSI. The only way to know for sure is by contacting one of the social security attorneys at disabilitycasereview.com. The social security attorneys at disabilitycasereview.com will explore the options that are available to you for receiving disability benefits.

Factor V Leiden thrombophilia gets its name from the city of Leiden in the Netherlands. The disease was first identified in Leiden by Professor R. Bertina et al in 1994.

It is unfortunate that factor V Leiden thrombophilia is a common inherited genetic disease. Somewhere around 5% of all Caucasians in North America are afflicted with this disease. Factor V Leiden thrombophilia is not as prevalent in Asians, Hispanics and Blacks.

As stated above, factor V Leiden thrombophilia is an inherited genetic disease. This disorder is the result of inheriting a mutated (defective) copy of the factor V gene. You will only have a slightly higher tendency to form abnormal blood clots if you inherit one copy of the defective gene (heterozygous) from one of your parents. Your tendency to develop abnormal blood cots will be significantly higher if you inherit a faulty gene (homozygous) from each of your parents.

There are other risk factors that may increase your likelihood of having factor V Leiden thrombophilia, besides inheriting the defective factor V gene. The primary ones are being Caucasian and of European descent.

It may be that you will never experience any signs or symptoms at all with factor V Leiden thrombophilia. However, if signs and symptoms do occur, they will probably be determined by whether your blood clot moves, where the blood clot travels in your body and where your blood clot forms.

Some of the signs and symptoms of a blood clot that develops close to the surface of your skin include:

  • Warmth
  • Redness
  • Tenderness or pain that you will usually feel in or around the vein where your blood clot has developed.

Some of the signs and symptoms of a blood clot that forms in a deep vein are:

  • Swelling that is prominent
  • Pain
  • Redness
  • Warmth.

Some of the signs and symptoms of a blood clot that moves to your lungs include:

  • Chest pain that takes place when you are breathing in
  • Shortness of breath that develops suddenly
  • A rapid heartbeat (tachycardia)
  • A cough that results in bloody or blood-streaked sputum.

 

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Frame Syndrome Osteomalacia and Receiving Social Security

Tuesday, January 17th, 2012

Osteoid is a bone protein matrix that is composed mainly of type 1 collagen. Osteoid builds up due to the fact that it does not mineralize properly when you have osteoblast or mineral dysfunction that is insufficient.

Your growth plate becomes irregular, thick and wide when the newly made bone of your growth plate does not mineralize. This results in a clinical diagnosis of rickets. This is true only in the case of children because adults do not have growth plates any longer.

Osteomalacia occurs when your remodeled bone does not mineralize. Osteomalacia is a condition that takes place in all ages. Many of the hereditary causes of osteomalacia show up during childhood and result in rickets.

Osteomalacia is characterized by a softening of your bones. In fact, that is what the meaning of osteomalacia is, “soft bones.”

Soft bones have a greater tendency to bow and fracture than harder, healthy bones do. When you have osteomalacia, your bone is prone to break down faster than it can re-form.

Osteomalacia and osteoporosis are not the same thing. Osteoporosis is another bone ailment that can also lead to bone fractures. Osteomalacia results from a defect in your bone-building process. Osteoporosis is caused by a weakening of previously constructed bone.

Frame syndrome is a rare kind of osteomalacia. It is a condition that is evidenced by an enzyme defect that affects bone formation. Frame syndrome mainly involves your ribs and your hip bone (iliac crest).

There is a racial predilection with frame syndrome. This condition takes place most of the time in Caucasians and blacks.

Frame syndrome is referred to in other ways. It is also called atypical osteomalacia involving the axial skeleton and axial osteomalacia.

In order for you to build strong, healthy bones, your body must have calcium and phosphate. Frame syndrome may develop if you do not receive enough of these two minerals from your diet or your body does not absorb these minerals properly.

There are several things that may result in these problems. Some of these things are:

  • Taking certain drugs that are used in the treatment of seizures, such as Phenobarbital and phenytoin
  • Having kidney or liver diseases
  • Having a Vitamin D deficiency
  • Having certain surgeries, such as gastrectomy (removing all or a part of your stomach)
  • Having an autoimmune disease that is known as celiac disease.

There are several signs and symptoms that you may have with frame syndrome. Some of these may include:

 

  • Tenderness that occurs over the area of your lumbar spine
  • A limited range of motion in the area of your spine
  • Back pain
  • Chronic axial pain that is vague
  • Fatigue that takes place in your extremities
  • Impairment in the formation of your bone
  • Osteomalacia of your hip bone (iliac crest)
  • Osteomalacia of your rib
  • Fragility of your bones
  • Weakness in your muscles
  • Weakness in your legs and arms
  • Diffuse body pains
  • A reduction in your ability to get around
  • A waddling gait when you walk.

 

 

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Infective Endocarditis and Disability Benefits

Tuesday, January 17th, 2012

There are four chambers and four valves that are located on the inside of your heart that are lined by a thin membrane that is known as the endocardium. Endocarditis is inflammation and/or infection of this inner layer of your heart. Endocarditis also usually affects your heart valves (prosthetic or native valves).

Infective endocarditis, which is also known as bacterial endocarditis is one of the kinds of endocarditis. Somewhere between 10,000 and 20,000 people are affected by infective endocarditis each year in the United States.

Even though infective endocarditis is not a common disease, it is a dangerous one. Even with antimicrobial therapy, infective endocarditis can result in the need for open heart surgery, stroke or even death.

Infective endocarditis is brought about by germs that get into your bloodstream, travel to your heart and attach themselves to damaged heart tissue or abnormal heart valves. In most cases of infective endocarditis, bacteria are the cause, but fungi or other microorganisms can also lead to the disease.

Sometimes, infective endocarditis may be caused by one of the many common bacteria that live in your upper respiratory tract, mouth or other areas of your body. In other instances, the organism that brings about this disease may get into your bloodstream through an infection or some other medical disorder, certain common everyday activities like brushing your teeth or chewing your food, the use of needles or catheters or having dental or respiratory tract procedures.

There are several risk factors that may increase your risk of getting infective endocarditis. These include:

  1. Any dental procedure
  2. IV drug use
  3. A congenital heart defect
  4. A prior episode of endocarditis
  5. Surgery on your urinary or gastrointestinal tracks
  6. Cardiomyopathy
  7. Having an artificial heart valve
  8. Scarring of your heart valve from rheumatic fever or other disorders
  9. Mitral valve prolapse with a good deal of abnormal backflow of blood (regurgitation)
  10. Procedures that involve your nose, ears and throat
  11. Bronchoscopy

The signs and symptoms that you may experience with infective endocarditis will vary according to the kind of the disease that you have and the cause of your infection. Possible signs and symptoms are:

 

  • Bumpy, painless nodules that appear on the soles of your feet and the palms of your hands
  • Weight loss that is unintentional
  • Joint pain or arthritis
  • Petechiae (these are tiny, purplish-red pinpoint spots of bleeding that are located under your skin)
  • A cough that is persistent
  • Headaches
  • Fever
  • Shortness of breath
  • Back or chest pain
  • Splinter hemorrhages (these are dark red lines of bleeding that are under your nails)
  • Chills
  • Oster’s nodes (these are tender spots under the skin on the pads of your fingers)
  • Night sweats.

There are other signs and symptoms that may be produced by infective endocarditis, which can only be seen and confirmed by your doctor. Some of these include:

  • Embolisms that are brought about by clumps of blood cells and infectious bacteria or fungi
  • A stroke
  • An enlarged spleen
  • A change in the quality of an existing heart murmur or a new heart murmur.

 

Are you no longer able to work because of disability that you have sustained due to complications that have resulted from infective endocarditis and/or other conditions that you have along with this disease? If this is the case, are you in need of financial help?

Have you made a request for Social Security disability benefits or disability benefits from the Social Security Administration? Has your request been denied by the Social Security Administration?

If you plan on reapplying or appealing your denial, you will need the help and advice of a disability attorney. The attorney at disabilitycasereview.com is the one to turn to.

Do not wait. Make your way to disabilitycasereview.com, without delay.

 

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Pulmonary Valve Stenosis and Receiving Disability

Monday, January 9th, 2012

 

The lower right chamber of your heart (your right ventricle) is what contracts and pushes blood from your heart and into your pulmonary artery. Your right ventricle does this when your heart squeezes. Your pulmonary artery is what transports blood from your heart to your lungs.

Your pulmonary valve lies between your main pulmonary artery and your right ventricle. Your pulmonary valve works to stop blood from leaking back into your heart in between the beats of your heart.

When there is nothing wrong with your pulmonary valve, it is composed of three thin leaflets. When there is a defect in your pulmonary valve, the condition is called pulmonary valve stenosis.

Pulmonary valve stenosis is evidenced by these leaflets being fused together, less than three or too thick. This causes a narrowing of your pulmonary valve. Because of this defect, it is more difficult for your heart to pump enough blood to the rest of your body.

The obstruction that results from pulmonary valve stenosis may just be minor or mild. In other instances, the obstruction may be moderate, severe or critical.

Pulmonary valve stenosis is usually caused by a defect that takes place while an unborn baby’s heart is being formed. This kind of a birth defect is what is referred to as congenital, which means that it is something that is present at birth. No one has yet been able to determine why this defect takes place.

When pulmonary valve stenosis occurs in older people, it is usually due to the placement of an artificial valve or other medical conditions. Some of these medical conditions from the heart defect are:

  • Carcinoid syndrome – This is a syndrome that is brought about by the release of a chemical that is known as serotonin. Growths that occur in your digestive system that are called carcinoid tumors are responsible for the release of serotonin. Carcinoid syndrome is marked by diarrhea and flushing of your skin.
  • Rheumatic fever – This is a disorder that is a complication of an infection that is the result of streptococcus bacteria like strep throat or scarlet fever.

There are some risk factors that may increase your likelihood of having pulmonary valve stenosis. Some of these risk factors include:

  • Having carcinoid syndrome
  • Having Noonan’s syndrome
  • Having rheumatic fever.

There are various signs and symptoms that may be an indication of pulmonary valve stenosis. These signs and symptoms usually depend on the degree to which your blood is being obstructed from flowing to your lungs from your right ventricle. Signs and symptoms are:

  • Loss of consciousness (fainting)
  • Chest pain
  • Fatigue
  • Shortness of breath, primarily with exertion
  • A heart murmur.

If pulmonary valve stenosis has resulted in your disability, you may be eligible for social security disability benefits like SSI or SSDI. The right thing to do is to go to disabilitycasereview.com and get the advice of one of the social security attorneys. The social security attorneys at disabilitycasereview.com are always ready to help you get the disability benefits that you deserve.

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Familial polyposis Coli and Receiving Social Security Disability

Monday, January 9th, 2012

Cancer is much larger and wider than one disorder. Cancer involves many different diseases. Cancer is marked by cells that are invasive (they invade and destroy adjacent tissue), aggressive (they grow and divide without respect to normal limits) and sometimes metastatic (they spread to other parts of the body).

There are many different forms of cancer. They are usually designated by where they start in your body. For instance, gall bladder cancer originates in your gall bladder. Kidney cancer starts in your kidneys. As you probably are aware, cancer may metastasize (spread) to other areas of your body, but it is still called by where it began in your body.

Colon cancer is one of the many forms of cancer. Colon cancer is also known as colorectal cancer. Colon cancer originates in your large intestine (colon). Rectal cancer starts in the last several inches of your colon. This is the part of your rectum that is close to your anus. When these cancers are considered together, they are known as colorectal cancers.

Familial polyposis coli is a kind of colorectal cancer. Familial polyposis coli is marked by anywhere from hundreds to thousands of polyps developing in your colon. If you have been diagnosed with familial polyposis coli, this may enable you to get social security disability benefits such as SSDI or SSI. What you really ought to do is to contact one of the social security attorneys at disabilitycasereview.com to see what they have to say. The social security attorneys at disabilitycasereview.com know how to deal with the Social Security Administration in the matter of disability benefits.

Familial polyposis coli is referred to in several other ways. It is also known as colon cancer, familial, FAP, Familial polyposis syndrome, polyposis coli, familial intestinal polyposis, familial multiple polyposis syndrome and MYH-associated polyposis, to name some of the other ways in which this disorder is designated.

Familial polyposis coli is an inherited colorectal cancer syndrome. Familial is used to show that this disease runs in families. Polyposis refers to the fact that anywhere from hundreds to thousands of polyps may form in your colon. Coli is used for bacteria that inhabits your colon or intestine.

The third most common form of cancer in both men and women in the United States is colon cancer. Familial polyposis coli accounts for somewhere around 1% of all the cases of colorectal cancer.

Familial polyposis coli is brought about by a mutation (defect) that occurs in the adenomatous polyposis APC (coli) gene that is located on chromosome No. 5. At the present time, no one knows for sure what leads to this defect taking place.

Familial polyposis coli may not result in any signs or symptoms at all. However, when the disorder progresses, some of the signs and symptoms that you may have include:

  • Diarrhea
  • Abdominal pain
  • A change in your bowel habits
  • Weight loss that is unintentional
  • Anemia (a lack of healthy red blood cells)
  • Bleeding that occurs from your rectum
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