Searching for Methylmalonic Acidemia Support information? Find all needed info by using official links provided below.
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 ...
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.verywellhealth.com/methylmalonic-acidemia-overview-4590107
Methylmalonic acidemia (MMA) is a rare and serious genetic disorder that affects multiple body systems. It can potentially cause coma and death, particularly if not correctly diagnosed and treated. Due to a genetic defect, the body is unable to properly process certain parts of proteins, leading to the symptoms of the condition.
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://rarediseases.info.nih.gov/diseases/3579/methylmalonic-acidemia-with-homocystinuria
21 rows · Oct 31, 2016 · Methylmalonic acidemia with homocystinuria is an inherited disorder in …
https://rarediseases.org/rare-diseases/acidemia-methylmalonic/
Methylmalonic Acidemia is a form of Ketotic Hyperglycinemia. (For more information on this disorder, choose “Ketotic Hyperglycinemia” as your search term in the Rare Disease Database.) Propionic Acidemia is a very rare genetic form of Ketotic Hyperglycinemia.
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