53. Leigh syndrome; mitochondrial. DD acute necrotising encephalitis (ANE), Japanese encephalitis
Вставка
- Опубліковано 30 вер 2024
- www.brainbitbybit.com/index-info
At 5 minutes I show 2 different patients with Leigh syndrome and their MRIs saying "it is reversible". instead of "It can be reversible".
@brain-bitbybit2009
#mitochondrialdisease #neuroradiology
Моя дочь скончалась от Синдрома Лея митохондриального заболевания , мутация NDUFA13 … к сожалению , лечения до сих пор нет ….
I used google translate to read your message: My condolences for your daughter.
There are many diseases that are labelled rare, without a cure and that is very difficult for patients and loved ones. I hope that explaining the mechanisms of all diseases, common and rare, increases the "general" knowledge of how the brain works. I hope that by lifting our level of knowledge the rare diseases reciprocally benefit as well. So that people with rare diseases feel less unseen.
Wishing you all the best.
What's the pronostic and what's the traitement
Thanks for watching.
Leigh is a heterogenous disease, so prognosis differs and treatment should be tailored to the underlying mutation/defect. If this is a personal question, your own doctor or specialist in the region where you live can help, explain and inform you.
In general this website is useful for MDs and patients: www.ninds.nih.gov/ with a section on Leigh syndrome and treatment.
For MDs: There was an interesting article in Neuropediatrics 2014 with review of long term survivors DOI: 10.1055/s-0034-1383823