Searching for Melas Syndrome Support information? Find all needed info by using official links provided below.
https://rarediseases.org/rare-diseases/melas-syndrome/
General Discussion. MELAS (Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-like episodes) syndrome is a rare disorder that begins in childhood, usually between two and fifteen years of age, and mostly affects the nervous system and muscles.
https://www.ncbi.nlm.nih.gov/books/NBK532959/
Mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) is a mitochondrial disease primarily affecting the nervous system and muscles. MELAS presents in children or young adults as recurrent episodes of encephalopathy, myopathy, headache, and focal neurological deficits. The condition is relentlessly progressive, resulting in neurological impairment by adolescence or ...
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!
http://www.newcastle-mitochondria.com/patient-and-public-home-page/melas/
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.sciencedirect.com/science/article/pii/S109671921530024X
MELAS syndrome is a frequent maternally inherited mitochondrial disorder. • The cardinal features are stroke-like episodes, encephalopathy, and myopathy. • Pathogenesis involves energy deficiency, angiopathy, and nitric oxide deficiency. • Management is largely symptomatic and should involve a multidisciplinary team. •Cited by: 202
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