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Saturday, June 9, 2012
Friday, June 8, 2012
What is kawasaki’s disease
What is kawasaki’s disease. Kawasaki
(KAH-wah-SAH-ke) disease is a rare childhood disease. It’s a form of a
disease called vasculitis (vas-kyu-LI-tis). In Kawasaki disease,
the walls of the blood vessels throughout the body become inflamed. The
disease can affect any type of blood vessel in the body, including the
arteries, veins, and capillaries.
In some cases, Kawasaki disease affects the coronary arteries, which carry oxygen-rich blood to the heart. As a result, a small number of children who have Kawasaki disease may develop serious heart problems. The cause of Kawasaki disease isn’t known. The body’s response to a virus or infection combined with genetic factors may cause the disease. However, no specific virus or infection has been found, and the role of genetics isn’t known.
The disease can’t be passed from one child to another. Your child
won’t get it from close contact with a child who has the disease. Also,
if your child has the disease, he or she can’t pass it to another child.
Kawasaki disease affects children of all races and ages and both genders. It occurs most often in children of Asian and Pacific Island descent. The disease is more likely to affect males, and most cases occur in children younger than 5 years old.
One of the main symptoms of this disease is a fever that lasts longer than 5 days. The fever remains high even after treatment with standard childhood fever medicines. Children who have the disease also may have red eyes, red lips, and redness on the palms of their hands and soles of their feet. These are all signs of inflamed blood vessels. Early treatment is important. It helps reduce the risk that Kawasaki disease will affect the coronary arteries and cause more serious problems.
Kawasaki disease can’t be prevented. However, most children who develop Kawasaki disease fully recover—usually within weeks of getting symptoms. Further problems are rare. In some children, the disease affects the coronary arteries. This can cause serious problems. These children need long-term care and treatment. Researchers continue to look for the cause of Kawasaki disease and better ways to diagnose and treat it. They also hope to learn more about long-term health risks, if any, for people who have had the disease. ( Definition from nhlbi.nih.gov with “What is kawasaki’s disease” )
In some cases, Kawasaki disease affects the coronary arteries, which carry oxygen-rich blood to the heart. As a result, a small number of children who have Kawasaki disease may develop serious heart problems. The cause of Kawasaki disease isn’t known. The body’s response to a virus or infection combined with genetic factors may cause the disease. However, no specific virus or infection has been found, and the role of genetics isn’t known.
One of the main symptoms of this disease is a fever that lasts longer than 5 days. The fever remains high even after treatment with standard childhood fever medicines. Children who have the disease also may have red eyes, red lips, and redness on the palms of their hands and soles of their feet. These are all signs of inflamed blood vessels. Early treatment is important. It helps reduce the risk that Kawasaki disease will affect the coronary arteries and cause more serious problems.
Kawasaki disease can’t be prevented. However, most children who develop Kawasaki disease fully recover—usually within weeks of getting symptoms. Further problems are rare. In some children, the disease affects the coronary arteries. This can cause serious problems. These children need long-term care and treatment. Researchers continue to look for the cause of Kawasaki disease and better ways to diagnose and treat it. They also hope to learn more about long-term health risks, if any, for people who have had the disease. ( Definition from nhlbi.nih.gov with “What is kawasaki’s disease” )
Venereal disease
Venereal disease. A disease that is contracted and transmitted by sexual contact, caused by microorganisms that survive on the skin or mucus membranes, or that are transmitted via semen, vaginal secretions, or blood during intercourse.
Because the genital areas provide a moist, warm environment that is especially conducive to the proliferation of bacteria, viruses, and yeasts, a great many diseases can be transmitted this way. They include AIDS, chlamydia, genital warts, gonorrhea, syphilis, yeast infections, and some forms of hepatitis.
Also known as a morbus venereus or sexually transmitted disease (STD).
( From medterms.com about Venereal disease )
Palm diseases
Palm diseases :
Bud Rots of Palm
Fusarium Wilt of Canary Island Date Palm
Fusarium Wilt of Queen Palm and Mexican Fan Palm
Ganoderma Butt Rot of Palms
Graphiola Leaf Spot (False Smut) of Palm
Leaf Spots and Leaf Blights of Palm diseases
Lethal Yellowing (LY) of Palm
Normal “Abnormalities” in Palms
Pestalotiopsis (Pestalotia) Diseases of Palm
Petiole (Rachis) Blight of Palm
Texas Phoenix Palm Decline
Thielaviopsis Trunk Rot of Palm diseases
Palm trees grown in the landscape appear carefree, but they are
susceptible to many diseases, insects and nutritional problems. Avoid
many of these problems a new batch of problems are out to get your
palms, but you can fight back. Insect pests and a number of diseases can
attack and damage palms and in extreme cases can kill them. If the
growing point of a palm is invaded by insects. Some leaf spot fungi move
in as secondary problems on palm leaves that are deficient in nutrients
or have received some sort of damage.
Bud Rots of Palm
Fusarium Wilt of Canary Island Date Palm
Fusarium Wilt of Queen Palm and Mexican Fan Palm
Ganoderma Butt Rot of Palms
Graphiola Leaf Spot (False Smut) of Palm
Leaf Spots and Leaf Blights of Palm diseases
Lethal Yellowing (LY) of Palm
Normal “Abnormalities” in Palms
Pestalotiopsis (Pestalotia) Diseases of Palm
Petiole (Rachis) Blight of Palm
Texas Phoenix Palm Decline
Thielaviopsis Trunk Rot of Palm diseases
The Genetic Epidemiology of Parkinson’s Disease
The Genetic Epidemiology of Parkinson’s Disease.
The cause of Parkinson’s disease (PD) is unknown. The major risk
factors identified to date are family history, age, and elements of
rural living. Nearly one-third of all PD cases are familial, a small
subset of which appears autosomal dominant; however, the majority
exhibit no clear inheritance pattern. Autosomal dominant PD is
genetically heterogeneous: two PD genes have been mapped to chromosomes 2
and 4 and there may be additional as yet unidentified genes.
The common forms of The Genetic Epidemiology of Parkinson’s Disease familial and sporadic cases-appear to involve a complex interplay of genetic susceptibility and environmental exposure. The observations that rural residence and pesticide exposure increase the risk of developing PD, and that a synthetic drug, 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine, can cause parkinsonism, suggest that at least a subset of PD may be caused by a toxin. Furthermore, modest but significant associations have been reported between PD susceptibility and genes that regulate metabolism of drugs and neurotoxins.
There is also evidence for mitochondrial dysfunction in PD, a finding
that was recently traced to anomalies in mitochondrial DNA. At the
present time, the genetics of PD appear to be complex, involving
multiple nuclear genes and possibly mitochondrial genes as well. ( From
ncbi.nlm.nih.gov about The Genetic Epidemiology of Parkinson’s Disease ).
The common forms of The Genetic Epidemiology of Parkinson’s Disease familial and sporadic cases-appear to involve a complex interplay of genetic susceptibility and environmental exposure. The observations that rural residence and pesticide exposure increase the risk of developing PD, and that a synthetic drug, 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine, can cause parkinsonism, suggest that at least a subset of PD may be caused by a toxin. Furthermore, modest but significant associations have been reported between PD susceptibility and genes that regulate metabolism of drugs and neurotoxins.
Thursday, June 7, 2012
Coronary heart disease symptoms artery
Coronary heart disease symptoms artery.
Coronary artery disease is atherosclerosis of the coronary arteries,
producing blockages in the vessels which nourish the heart itself.
Atherosclerosis occurs when the arteries become clogged and narrowed, restricting blood flow. Without adequate blood flow from the coronary arteries, the heart becomes starved of oxygen and vital nutrients it needs to work properly.
Coronary heart disease (CHD), also called Coronary heart disease symptoms artery. Without quick treatment,
a heart attack can lead to serious problems and even death. If your
coronary arteries become partially blocked, it can cause chest pain
(angina). In some cases, people may not have symptoms
of coronary heart disease. Shortness of breath is most often a symptom
of cardiac or pulmonary (lung) disorders. Heart failure and coronary
artery disease frequently produce shortness. Treatment for Coronary heart disease symptoms artery depends upon how far the disease has already progressed. Coronary artery disease is the buildup of plaque.
Heart pain, caused by plaque in the arteries, is often one of the first symptoms of coronary artery disease (CAD). Some people who have coronary artery disease and insufficient blood flow to the heart muscle (ischemia) do not have any symptoms. Many people have no symptoms of coronary artery disease before having a heart attack; 63% of women and 48% of men who died suddenly of Coronary heart disease symptoms artery.
Atherosclerosis occurs when the arteries become clogged and narrowed, restricting blood flow. Without adequate blood flow from the coronary arteries, the heart becomes starved of oxygen and vital nutrients it needs to work properly.
Heart pain, caused by plaque in the arteries, is often one of the first symptoms of coronary artery disease (CAD). Some people who have coronary artery disease and insufficient blood flow to the heart muscle (ischemia) do not have any symptoms. Many people have no symptoms of coronary artery disease before having a heart attack; 63% of women and 48% of men who died suddenly of Coronary heart disease symptoms artery.
Crohn’s disease life expectancy
Crohn’s disease life expectancy. Having Crohn’s Disease doesn’t mean that you are going to drop dead tomorrow, or have a life ten years shorter than everyone else. People with Crohn’s Disease have a relatively normal life expectancy compared to the general population.
You may need to make lifestyle changes to make sure that your Crohn’s disease life expectancy in remission, but on the whole people with Crohn’s Disease can do anything that they put their minds to.
The risk of dying from an acutely serious attack of Crohn’s Disease in this day and age is relatively low. If you had Crohn’s Disease in the 1950’s the risk of death due to a serious attack of Crohn’s was well over 30 percent! ( Detail from healcrohnsnow.com about Crohn’s disease life expectancy )
Crohn’s disease rash
Crohn’s disease rash. Hartnup disease a hereditary disorder of intestinal and renal transport of neutral ?
-amino acids, marked by a pellagra-like skin rash, with transient cerebellar ataxia, constant renal aminoaciduria, and other biochemical abnormalities.
People with Crohn’s disease rash also experience rashes, arthritis, and swollen eyes. The condition is an inflammatory bowel disease. Crohn’s disease can cause symptoms outside the digestive tract, such as joint pain, eye problems, a skin rash, or liver disease. The three most common sites of intestinal involvement in Crohn’s disease are rashes, arthritis, inflammation of the eye, tiredness, and lack of concentration.
Some individuals with Crohn’s disease rash
also develop symptoms outside of the gastrointestinal tract; these
symptoms include arthritis, skin rash, and inflammation. Crohn’s disease
(regional enteritis, granulomatous ileitis, ileocolitis) is a chronic.
Some people have reactions such as fever or rash during the infusion. Crohn’s disease rash.
-amino acids, marked by a pellagra-like skin rash, with transient cerebellar ataxia, constant renal aminoaciduria, and other biochemical abnormalities.
People with Crohn’s disease rash also experience rashes, arthritis, and swollen eyes. The condition is an inflammatory bowel disease. Crohn’s disease can cause symptoms outside the digestive tract, such as joint pain, eye problems, a skin rash, or liver disease. The three most common sites of intestinal involvement in Crohn’s disease are rashes, arthritis, inflammation of the eye, tiredness, and lack of concentration.
Crohn’s disease symptoms description
Crohn’s disease symptoms description.
The commonest Crohn’s disease definition is that it is a form of
inflammatory bowel disease that makes the patient’s intestinal tract
swell up and in addition, it can cause restricted functioning of that
part of the body as well.
In fact, from available Crohn’s disease symptoms description it is also clear that one should make an effort to find out more about what inflammatory bowel diseases are all about so that one is in a better position to understand the true meaning of Crohn’s disease as well as figure out what the consequences of suffering from the disease are.
However, one thing is clear and that is that the medical fraternity
has not as yet been able to fathom why a patient’s gastrointestinal
tract becomes inflamed though according to findings of researchers, it
seems that it is a failure of the immune system that can cause such
inflammation and thus lead people to start looking for Crohn’s disease
definitions. ( Detail from crohnsdiseasetoday.com on Crohn’s disease symptoms description )
In fact, from available Crohn’s disease symptoms description it is also clear that one should make an effort to find out more about what inflammatory bowel diseases are all about so that one is in a better position to understand the true meaning of Crohn’s disease as well as figure out what the consequences of suffering from the disease are.
Gaucher disease pathway
Gaucher disease pathway. In relation to Gaucher’s disease, initial results of enzymatic complementation were disappointing, but the reason for this was soon established. Crude enzyme preparations obtained from human tissues such as the placenta were not taken up by non?parenchymal hepatic cells. This occurred because the enzyme preparations did not harbour the appropriate glycoprotein targeting sequences for uptake by membrane receptors leading to delivery to the nascent organelle.
Mannosephosphate Gaucher disease pathway residues are typically found on nascent lysosomal membranes, and are components of the pathway for endogenous and exogenous delivery of a large class of lysosomal proteins. This pathway is not in fact the relevant pathway for delivery of nascent glucocerebrosidase, which is a lysosomal membrane protein. Later, with the discovery of the macrophage mannose receptor, deglycosylation of purified preparations of human tissue glucocerebrosidase to reveal terminal mannose residues was successful in facilitating uptake of the enzyme molecules by enriched populations of macrophages.
Gaucher disease type 1
. A definitive diagnosis is made with genetic
testing. As there are numerous different mutations, sequencing of the
beta-glucosidase gene is sometimes necessary to confirm the diagnosis.
Prenatal diagnosis is available, and is useful when there is a known
genetic risk factor.
A diagnosis Gaucher disease type 1 can also be implied by biochemical abnormalities such as high alkaline phosphatase, angiotensin-converting enzyme (ACE) and immunoglobulin levels, or by cell analysis showing “crinkled paper” cytoplasm and glycolipid-laden macrophages.
Some lysosomal enzymes are elevated, including tartrate-resistant
acid phosphatase, hexosaminidase, and a human chitinase,
chitotriosidase. This latter enzyme has proved to be very useful for
monitoring Gaucher’s disease activity in response to treatment, and may
reflect the severity of the disease. ( Wikipedia diagnosis article on Gaucher disease type 1 )
A diagnosis Gaucher disease type 1 can also be implied by biochemical abnormalities such as high alkaline phosphatase, angiotensin-converting enzyme (ACE) and immunoglobulin levels, or by cell analysis showing “crinkled paper” cytoplasm and glycolipid-laden macrophages.
Gaucher’s disease Type I effect
Gaucher’s disease Type I effect
(or non-neuropathic type) is the most common form of the disease,
occurring in approximately 1 in 50,000 live births. It occurs most often
among persons of Ashkenazi Jewish heritage. Symptoms may begin early in
life or in adulthood and include enlarged liver and grossly enlarged
spleen (together hepatosplenomegaly); the spleen can rupture and cause
additional complications.
Skeletal Gaucher’s disease Type I effect and bone disease may be extensive. Spleen enlargement and bone marrow replacement cause anemia, thrombocytopenia and leukopenia. The brain is not affected pathologically, but there may be lung and, rarely, kidney impairment.
Patients in this group usually bruise easily (due to low levels of
platelets) and experience fatigue due to low numbers of red blood cells.
Depending on disease onset and severity, type 1 patients may live well
into adulthood. Many patients have a mild form of the disease or may not
show any symptoms. ( Definition wikipedia about Gaucher’s disease Type I effect ).
Skeletal Gaucher’s disease Type I effect and bone disease may be extensive. Spleen enlargement and bone marrow replacement cause anemia, thrombocytopenia and leukopenia. The brain is not affected pathologically, but there may be lung and, rarely, kidney impairment.
Wednesday, June 6, 2012
Justin Bieber Style House at Los Angeles
Justin Bieber Style House at Los Angeles. The house
features plenty of celebrity house styles amenities: glass chandeliers,
retractable glass walls, gourmet kitchen, gym and massage room.
Justin Bieber Style House keeping with the California house style, the house features several outdoor spaces with enclosed gardens, terraces, and outdoor rooms.
The only thing holding Justin Bieber back from moving in immediately is the previous tenant. As reported earlier, the rumor is that Ashton Kutcher has been renting this Style House for $50,000 a month.
If the Justin Bieber take the Justin Bieber Style House with a classic mortgage, Justin Bieber can expect a monthly payment of $39,979, assuming a 20 % downpayment on a 30-year-fixed-rate mortgage.
Justin Bieber Style House keeping with the California house style, the house features several outdoor spaces with enclosed gardens, terraces, and outdoor rooms.
The only thing holding Justin Bieber back from moving in immediately is the previous tenant. As reported earlier, the rumor is that Ashton Kutcher has been renting this Style House for $50,000 a month.
If the Justin Bieber take the Justin Bieber Style House with a classic mortgage, Justin Bieber can expect a monthly payment of $39,979, assuming a 20 % downpayment on a 30-year-fixed-rate mortgage.