Searching for Melas Support information? Find all needed info by using official links provided below.
https://ghr.nlm.nih.gov/condition/mitochondrial-encephalomyopathy-lactic-acidosis-and-stroke-like-episodes
Oct 29, 2019 · Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) is a condition that affects many of the body's systems, particularly the brain and nervous system (encephalo-) and muscles (myopathy).The signs and symptoms of this disorder most often appear in childhood following a period of normal development, although they can begin at any age.
https://rarediseases.org/rare-diseases/melas-syndrome/
MELAS syndrome is a rare disorder that affects males and females in equal numbers. Although rare, MELAS syndrome is probably the most common type of mitochondrial myopathy caused by …
https://www.medicinenet.com/melas_syndrome/article.htm
MELAS syndrome, a rare form of dementia, is caused by mutations in the genetic material (DNA) in the mitochondria. Melas symptoms include brain dysfunction (encephalopathy) with seizures and headaches, muscle disease with lactic acid build-up in the blood, temporary …
http://www.newcastle-mitochondria.com/patient-and-public-home-page/melas/
This is one of the most common causes of mitochondrial disease. Patients with this mutation have variable disease manifestations ranging from no symptoms at all, to being quite severely affected with the syndrome called MELAS , this is the short name for a collection of symptoms calledmitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes.
https://www.diseasemaps.org/melas-syndrome/organization/129
MELAS Syndrome International Support Group is created for all MELAS patients in the world. The purpose is to exchange MELAS-related information and experiences so that the knowledge and the strength we receive from each other actually benefits our lives!
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3789935/
Jan 28, 2013 · The discussed patient is now under control of the Clinic of Metabolic Diseases and under the following medication: coenzyme Q10 and L-arginine, which were proved to support the metabolism of cells affected by mitochondrial tRNA mutation in MELAS syndrome [3,7,8].
https://www.ncbi.nlm.nih.gov/books/NBK532959/
MELAS is a mitochondrial inherited genetic disorder. Paternal mitochondria are present only in the tailpiece of the sperms. As a result, they are lost during fertilization and mitochondrial disorders including MELAS are maternally inherited. In rare instances, MELAS may …
http://www.medlink.com/article/melas
• The clinical hallmark of MELAS is stroke-like episodes that usually affect young people (typically before age 40) and do not conform to large vessel territories. • Although 30 different mitochondrial DNA mutations have been associated with MELAS, about 80% of patients harbor an m.3243A>G mutation.
https://en.wikipedia.org/wiki/MELAS
Mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) is one of the family of mitochondrial cytopathies, which also include MERRF, and Leber's hereditary optic neuropathy.It was first characterized under this name in 1984. A feature of these diseases is that they are caused by defects in the mitochondrial genome which is inherited purely from the female parent.Specialty: Neurology
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