Tuesday, March 22, 2011

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Monday, March 14, 2011

Dieticians - Internists - Is kwashiorkor a possible symptom of our poor diet - too much white flour / corn syr?

Question by Cordelia: Dieticians - Internists - Is kwashiorkor a possible symptom of our poor diet - too a lot white flour / corn syr?
I think several Americans are starving themselves due to the fact of their daily reliance on white flour for sustenance, whether or not rich or poor. Does white flour inhibit excellent digestion of other more protein rich foods? (Look at all the protruding bellies.) I'm looking at some thing that indicated that in a report as follows:

"Conditions listing Kwashiorkor as a symptom may possibly also be possible underlying causes of Kwashiorkor. Our database lists the following as having Kwashiorkor as a symptom of that condition:
Alcoholism
Amphetamine abuse
Amyloidosis AL
Anorexia Nervosa
Blind loop syndrome
Boyd-Stearns syndrome
Brinton disease
Classic galactosemia
Cocaine fetopathy
Congenital short bowel
Congenital sucrose-isomaltose malabsorption
Cutaneous photosensitivity colitis, lethal
Cystic Fibrosis
Epidermolysis bullosa, junctional
Finnish nephrosis syndrome
Follicular hamartoma - alopecia - cystic fibrosis
Gastrointestinal amyloidosis
Hereditary amyloidosis
Hyperemesis Gravidarum
Intestinal epithelial dysplasia
Intractable diarrhea with enterocytes assembly abnormalities, congenital, familial
Juvenile tropical pancreatitis syndrome
Microsporidiosis
Obal syndrome
Opisthorchiasis
Pancreatic insufficiency
Pancreatic Islet Cell Cancer
Patau syndrome
Sandifer syndrome
Self Harm
Short Bowel Syndrome
TopDrug interactions causing Kwashiorkor:
When combined, specific drugs, medications, substances or toxins may possibly react causing Kwashiorkor as a symptom.
The list below is incomplete and numerous other drugs or substances could trigger your symptoms. Constantly advise your physician of any medications or treatments you are making use of, including prescription, over-the-counter, supplements, herbal or option treatments.
Chloramphenicol and Acetaminophen interaction
far more interactions...»
Read a lot more about medication causes of Kwashiorkor
TopMedical news summaries relating to Kwashiorkor:
The following medical news items are relevant to causes of Kwashiorkor:
Celiac disease a lot more typical than thought
Commonly confused celiac illness
Hyperemesis symptoms similar to morning sickness
Operation possibilities for obesity
Prevention of osteoporosis in cystic fibrosis
TopRelated details on causes of Kwashiorkor:
As with all medical conditions, there might be several causal factors. Further relevant info on causes of Kwashiorkor might be found in:
Risk factors for Kwashiorkor
Hidden causes of Kwashiorkor
TopCauses of Kwashiorkor: On-line Medical Books
16 MEDICAL BOOKS On the internet! Review excerpts from medical books on the internet, no cost, without having registration, for much more information about the causes of Kwashiorkor.
Protein-calorie malnutrition: Causes and incidence
(Expert Guide to Diseases (Eighth Edition))
Both kwashiorkor (edematous PCM) and marasmus (nonedematous PCM) are frequent in underdeveloped countries and in areas in which dietary amino acid
content is insufficient to satisfy growth requirements. Kwashiorkor normally occurs at about age 1, following infants are weaned from breast milk to a protein-deficient diet of starchy gruels or sugar water, but it can develop at any time throughout the formative years. Marasmus affects infants ages 6 to 18 months as a result of breast-feeding failure, or a debilitating condition such as chronic diarrhea.
In industrialized countries, PCM may occur secondary to chronic metabolic disease that decreases protein and calorie intake or absorption, or trauma that increases protein and calorie requirements. In the United States, PCM is estimated to occur to some extent in 50% of elderly folks in nursing homes. Those who aren’t allowed anything by mouth for an extended period are at high risk of developing PCM. Conditions that boost protein-calorie requirements incorporate severe burns and injuries, systemic infections, and cancer (accounts for the largest group of hospitalized patients with PCM). Conditions that cause defective utilization of nutrients consist of malabsorption syndrome, short-bowel syndrome, and Crohn’s illness.
Protein-calorie malnutrition: Causes
(Handbook of Diseases)
Both marasmus (nonedematous protein-calorie malnutrition) and kwashiorkor (edematous protein-calorie malnutrition) are typical in underdeveloped countries and in areas where dietary amino acid content is insufficient to satisfy growth requirements. Kwashiorkor normally occurs at about age 1, right after infants are weaned from breast milk to a protein-deficient diet plan of starchy gruels or sugar water, but it can develop at any time during the formative years. Marasmus affects infants ages 6 to 18 months as a result of breast-feeding failure or a debilitating condition such as chronic diarrhea.
In industrialized countries, protein-calorie malnutrition may possibly occur secondary to chronic metabolic disease that decreases protein and calorie intake or absorption or trauma that increases protein a


Greatest answer:

Answer by Pityblues pray Airline safety
Interesting read and yes, you have a valid point there.
I believe when manufactures add or take goods out to produce a longer shelf life, we turn into unwittingly victims.
I also will state that man's desire to consume these goods in large quantities also makes a statement to how well they care about their own bodies and for that reason allowing them to turn into the blimps, encourage laziness and less outgoing as a person.
I discover these chemicals are foreign to the human body and instead of helping ones digestion, truly does the opposite. It promotes construct up and as a result a blockage to the body operating normally.
There is where the several issues of the body lies in wait for us. Some times quicker then we ever could understand.
It is sad that a lot of of these traits are passed on in the course of breast feeding and actual Development inside a mother's womb. Nonetheless i wonder if this wasn't all a style by human engineering to cause a decrease in the human population or is it just a consequence of a "on Demand" society.
I learned a lot about nutritional values when i searched out about diets for myself. There are some products now that i will in no way eat once more
Great question and deserving my further attention as well as other people.



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Q&A: Does anyone know of a good online support group for Amyloidosis?

Question by aussygirl87: Does any person know of a good online support group for Amyloidosis?
I am a 22yr old female recently diagnosed with Amyloidosis, I have been looking for a local or nearby support group and I can't discover 1. So now I'm looking for a excellent on-line support group.


Greatest answer:

Answer by Patio of Enjoyable
I was caregiver and advocate for my sister when she went through treatment for amyloidosis at the Fred Hutchins Center in the Seattle Cancer Care Alliance ( SCCA ) last fall. The condition is really rare, there may possibly not be a support group in existence for it.

http://www.seattlecca.org/diseases/amyloidosis.cfm

http://www.mayoclinic.org/amyloidosis/

http://www.fhcrc.org/patient/treatment/trials/index.php?atn=detail&id=6961

http://www.clinicaltrials.gov/ct/search?term=NCT00064337

http://www.seattlecca.org/



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A Silent Killer Disease Threatens Eight in a Million Annually

A Silent Killer Disease Threatens Eight in a Million Annually











Austin, TX (PRWEB) February 24, 2006

Scientists know that heart disease is the #1 killer, cancer is the #1 fear, and Alzheimer’s is the #1 concern of Americans. Scientists also know that AIDS, Eczema, and Hodgkin’s Disease are immune system diseases but little is recognized about the rare immune system illness that threatens eight in a million people annually.


Primary amyloidosis is a disease caused by the abnormal accumulation of protein molecules in body tissues. These proteins are small fragments of antibody molecules, which are normally present in the blood, give protection against infectious agents and bacteria. Nevertheless, in primary amyloidosis a defect occurs in the immune system where excessive amounts of antibody molecules are produced and deposited in the tissues. These tissue deposits enlarge and damage typical tissues practically in every organ of the body. As the tissues continue to enlarge they interfere with regular body functions causing kidney failure, heart failure, or loss of sensation to extremities and motor function. There is no distinct treatment for primary amyloidosis that has been proven to be powerful and outcomes in prolonged survival.


The cause of primary amyloidosis is unknown and often misdiagnosed due to the fact the symptoms are similar to other diseases (e.g. heart illness, cancer, gastrointestinal illness.) Primary amyloidosis affects both girls and men with peak occurrence around age 60-65, but numerous patients get the disease in their 40’s and 50’s.


Clyde Slappey was diagnosed having primary amyloidosis when he was 42 years old. Doctors had given up on him, but he and his wife, Deborah, fought for a cure. On November 12, 1994, their journey with this disease began. Clyde and Deborah traveled around the country and visited many physicians and hospitals, Though numerous thought Clyde was beyond support, the couple did not accept “no” for an answer. “After the prognosis at the local hospital, things just didn’t appear too well for Clyde,” Deborah claims. “I knew that I required to do some thing. I just didn’t feel that enough was being accomplished specially when we had so little details about the disease.”


Clyde and Deborah knew that they had a race against time. Based upon the physician’s prognosis, Clyde didn’t have but a year or so to live since of the aggressive nature of the primary amyloid illness. In a desperation move, knowing they had no choice, the two of them pursued every single chance to discover somebody who would be able to assist Clyde. On February 14, 1995, they made it to the Mayo Clinic.


But Clyde’s body grew weaker. He waited 57 days for a heart transplant, but it was too a lot time to wait. He died inside two weeks of receiving a life-saving heart transplant at The Mayo Clinic.


Deborah Slappey Pitts chronicles their struggle to keep Clyde alive in a moving book “I Feel Okay.” It is a moving testament to the power of the human spirit that encourages people to fight for a solution regardless of overwhelming odds. “I watched his faith strengthen to its highest degree, and I know it was well with his soul as he closed his eyes in sleep,” Deborah laments. “I won’t ever forget that moment in the hospital room. And a lot of me remained in that hospital room as I said goodbye to my companion, my Innisfree, my life.”


Deborah resides in Columbus, Georgia with her husband, Marshall Pitts. She holds a B.S. degree in Marketing from Georgia Southwestern University, and an M.B.A from Albany State University. She is an associate director of software testing at TSYS, Inc. “I Feel Okay” (ISBN 1420806084, AuthorHouse, 2005) might be bought at any bookstore worldwide.


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I have a question about a disease called Amyloidosis. My mom died from this disease over 10 years ago.?

Question by Tareksgirl64: I have a question about a disease referred to as Amyloidosis. My mom died from this illness over 10 years ago.?
I have been performing some study on line about it, and I discovered out that there is a lot more than 1 kind of this, and I have no clue what kind my mom had, and I want to know if I am at risk. The physician said that it is extremely rare, and there is no cure. If there are any doctors or nurses here, I would appreciate any help you can provide. Thanks in advance!
I guess I require to mention that the physician who diagnosed her took a biopsy from her liver? Sorry I left that out. Thanks!


Finest answer:

Answer by lab rat
There are quite a couple of differenct varieties of amyloidosis, but the vast majority of them are not inherited. They are mostly very rare, and many have no cure, so it doesn't narrow it down truly.

Amyloidosis is caused by abnormal proteins. Proteins are like bits of string that fold up into 3D shapes - each diverse kind of protein has its own distinctive shape. In amyloidosis, a protein loses its typical shape and takes on an abnormal form that builds up and causes damage in the body. What kind of amyloidosis a individual has depends on what particular protein is involved.

Alzheimer's illness is the most frequent sort of amyloidosis, although this almost certainly isn't what affected your Mom, because it's normally just referred to as 'Alzheimer's disease', not an amyloidosis. Another well-known one is light chain amyloidosis (occasionally called primary amyloidosis)- this is caused by a protein that is part of antibodies. It can occur when somebody has a blood cell disorder like lymphoma or myeloma, or it can occur by itself. It tends to affect the kidneys and the heart. Another one is 'A amyloidosis' (at times known as secondary amyloidosis)- this tends to occur when an individual has some kind of chronic inflammation going on. It tends to affect the heart, liver and spleen. Then there are the much less common ones like lysozyme and transthyretin amyloidosis, which can rarely be inherited.

Your greatest option is to attempt and speak to an individual involved in your mother's care, or to see if you can access her medical record or death certificate. You could also speak to other folks in your family to see if anyone else has had the exact same condition - the hereditary ones tend to have a very strong family history. The problem with amyloidoses is that unless you are medically trained, numerous of them appear to have fairly comparable symptoms (e.g. heart and kidney issues), so it's fairly tough to work out which one it may well have been.

This web site has some excellent info:
http://www.emedicine.com/med/topic3377.htm





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VA Extends 'Agent Orange' Benefits to More Veterans Parkinson?s Disease, Two Other Illnesses Recognized

VA Extends 'Agent Orange' Advantages to Much more Veterans Parkinson’s Disease, Two Other Illnesses Recognized












Washington (Vocus) October 15, 2009

Relying on an independent study by the Institute of Medicine (IOM), Secretary of Veterans Affairs Eric K. Shinseki decided to establish a service-connection for Vietnam Veterans with 3 certain illnesses based on the latest evidence of an association with the herbicides referred to Agent Orange.


The illnesses affected by the recent decision are B cell leukemias, such as hairy cell leukemia Parkinson’s disease and ischemic heart illness.


Employed in Vietnam to defoliate trees and remove concealment for the enemy, Agent Orange left a legacy of suffering and disability that continues to the present. Between January 1965 and April 1970, an estimated 2.6 million military personnel who served in Vietnam were potentially exposed to sprayed Agent Orange.


In practical terms, Veterans who served in Vietnam throughout the war and who have a “presumed” illness don’t have to prove an association between their illnesses and their military service. This “presumption” simplifies and speeds up the application method for positive aspects.


The Secretary’s decision brings to 15 the number of presumed illnesses recognized by the Department of Veterans Affairs (VA).


“We should do far better reviews of illnesses that may be connected to service, and we will,” Shinseki added. “Veterans who endure well being troubles deserve timely decisions based on solid evidence.”


Other illnesses previously recognized under VA’s “presumption” rule as becoming caused by exposure to herbicides during the Vietnam War are:


Acute and Subacute Transient Peripheral Neuropathy
AL Amyloidosis

Agent Orange 2/2/2/2


Chloracne
Chronic Lymphocytic Leukemia
Diabetes Mellitus (Sort 2)
Hodgkin’s Illness
Several Myeloma
Non-Hodgkin’s Lymphoma
Porphyria Cutanea Tarda
Prostate Cancer
Respiratory Cancers, and
Soft Tissue Sarcoma (other than Osteosarcoma, Chondrosarcoma, Kaposi’s sarcoma, or Mesothelioma)

Extra data about Agent Orange and VA’s services and programs for Veterans exposed to the chemical are obtainable at http://www.publichealth.va.gov/exposures/agentorange.


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Histopathology Kidney --Amyloidosis






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Combination heart-kidney transplants are rare only a little number of hospitals in the US and Europe do these procedures. David Gildea is the first person in Nebraska to have this dual transplant. Suffering from the rare blood illness Amyloidosis, Gildea had only months to live when his doctors determined they could transplant his failing heart and kidneys. Surviving the organ transplant was only his initial step. Gildea still wants a bone marrow transplant to beat the disease. He is planning to have that transplant at The Nebraska Medical Center as well. David, along with his girlfriend and his daughter joined members of his medical team at the medical center June 1st, 2010 to talk about this milestone transplant. The Nebraska Medical Center is property to an internationally recognized transplant program, specializing in solid organ transplant as well as bone marrow and stem cell transplantation. For more data, call 1-800-922-0000 or pay a visit to www.nebraskamed.com.

Hypertrophic cardiomyopathy and symptomatic conduction system disease in cardiac amyloidosis.(Case Report)(Clinical report): An article from: Southern Medical Journal

Hypertrophic cardiomyopathy and symptomatic conduction system illness in cardiac amyloidosis.(Case Report)(Clinical report): An write-up from: Southern Medical Journal

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Citation Details
Title: Hypertrophic cardiomyopathy and symptomatic conduction system illness in cardiac amyloido

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Made it to the Vet Hospital
kidney amyloidosis
Image by joannamkay
It's been a pretty traumatic day for us kittehs! (

Jasper was transferred to Strathfield Animal Hospital these days for further tests and to see a specialist. We raced him up there this arvo - just in time to catch the vet just before the end of the week.

So far there isn't a definitive answer about what's wrong with him, but he does have non-regenerative anaemia - which is not a good sign.

Vet says it's likely either Glomerulonephritis which is a yucky dilemma with his kidneys but treatable or it could be Amyloidosis which is a heriditary condition and not treatable. It could also be a form of leukaemia.

This afternoon he had a blood transfusion and an ultrasound to get a very good look at his kidneys. He'll possibly have a bone marrow test and a kidney biopsy on Monday.

We'll know a lot more in a few days or so. For now.. cross your fingers and paws for us!!