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https://ghr.nlm.nih.gov/condition/propionic-acidemia
Oct 15, 2019 · Propionic acidemia is an inherited disorder in which the body is unable to process certain parts of proteins and lipids (fats) properly. It is classified as an organic acid disorder, which is a condition that leads to an abnormal buildup of particular acids known as organic acids.
The world's leading source for Organic Acidemia metabolic disorder support and information. Welcome to the Organic Acidemia Association. We are a volunteer non-profit organization whose mission is to empower families and health care professionals with knowledge in organic acidemia metabolic disorders. We support early intervention through ...
https://ghr.nlm.nih.gov/condition/methylmalonic-acidemia
Oct 29, 2019 · Methylmalonic acidemia is an inherited disorder in which the body is unable to process certain proteins and fats (lipids) properly. The effects of methylmalonic acidemia, which usually appear in early infancy, vary from mild to life-threatening.Affected infants can experience vomiting, dehydration, weak muscle tone (hypotonia), developmental delay, excessive tiredness (lethargy), an enlarged ...
https://rarediseases.info.nih.gov/diseases/7033/methylmalonic-acidemia
Jan 27, 2020 · •Methylmalonic acidemia refers to a group of inherited conditions in which the body can’t breakdown certain parts of proteins and fats. This leads to a build-up of toxic substances and to bouts of serious illness called decompensation events or metabolic crises.
https://www.diseaseinfosearch.org/disease/4713/support
The Organic Acidemia Association is a volunteer non-profit organization whose mission is to empower families and health care professionals with knowledge in organic acidemia metabolic disorders. We support early intervention through expanded newborn screening, solicit contributions and …
https://www.verywellhealth.com/propionic-acidemia-overview-4177298
Oct 23, 2018 · Propionic acidemia is a disease with risks requiring ongoing management, however, many people with the condition go on to lead full lives. Don’t hesitate to reach out to your friends, family members, and healthcare team to get the support you need.
https://www.oaanews.org/ga-i.html
Glutaric acidemia type 1 is an inherited disorder in which the body is unable to process certain proteins properly. People with this disorder have inadequate levels of an enzyme that helps break down the amino acids lysine, hydroxylysine and tryptophan, which are building blocks of protein.
https://www.verywellhealth.com/methylmalonic-acidemia-overview-4590107
Methylmalonic acidemia is a rare and sometimes fatal disease resulting from a genetic problem in metabolism. Learn more about symptoms and treatment. ... Without support, individuals may die during these periods. These might happen before an initial diagnosis or at other periods of stress or illness. These individuals need intensive support in ...
https://rarediseases.info.nih.gov/diseases/6522/glutaric-acidemia-type-i
Apr 18, 2017 · Glutaric acidemia type I (GA1) is a genetic metabolic disorder.People with GA1 don't make enough of one of the enzymes needed to break down certain amino acids found in the proteins we eat. Without enough of the enzyme, the breakdown products of these amino acids build up in tissues of the body. The buildup of these chemicals can damage the brain, especially the area of the brain called the ...
https://www.ncbi.nlm.nih.gov/pubmed/30080956
Propionic acidemia (PA) and methylmalonic acidemia (MMA) comprise the most common organic acidemias and account for profound morbidity in affected individuals. Although liver transplantation (LT) has emerged as a bulk enzyme-replacement strategy to stabilize metabolically fragile patients, it is not a metabolic cure because patients remain at ...Cited by: 7
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