Rett Syndrome | Cellular and molecular basis of Rett syndrome | Treatment of Rett Syndrome.
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- เผยแพร่เมื่อ 15 ต.ค. 2024
- This video talks about Rett Syndrome | Cellular and molecular basis of Rett syndrome | Treatment of Rett Syndrome.
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Thanks this is perhaps the best explanation of RED syndrome that I have seen.
Could you please help me by sharing my contents with your friends group/ college group. I put huge efforts in making these videos but unfortunately not a lot of people are watching this.
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Could you please help me by sharing my contents with your friends group/ college group. I put huge efforts in making these videos but unfortunately not a lot of people are watching this.
Another great video! I have one question though: as PSD95 is present in glutamatergic/excitatory neurons, wouldn't that mean that excitatory transmission is disturbed because of the loss of post-synaptic spines? How is that linked to overall too much excitation (E/I (im)balance) in Rett syndrome though? Or did I misunderstand something there? I'd be curious to know if you have an answer :) Thank you!
PSD95 stabilizes and regulates excitatory synaptic receptors, crucial for synaptic plasticity and strength. It indirectly influences inhibitory synapses to maintain excitatory/inhibitory balance. Dysregulation of PSD95 is linked to disorders like autism and schizophrenia, underscoring its importance in neural circuit stability and overall brain function. For more details refer to this research article. www.ncbi.nlm.nih.gov/pmc/articles/PMC2526002/#:~:text=AMPA%20receptors%20directly%20associate%20with,decreased%20excitation%2C%20or%20increased%20inhibition.
Excellent Narration about the Rett...so far never posted. CONGRATS. can u pl. Inform me, how to proceed about it for treatment,since my daughter is having same complaint. Please help us....Awaiting Sir.
This FDA approved drug is now available in USA market. Email the the company such that you can import it in India
Hello, is it diagnosed or are you assuming by symptoms?
My daughter have Rett syndrome. She has 18yrs old.she can't do nothing. I am very happy to know this medicine. IS it available in india. Please reply
I am unsure that it's available in india. Can you please email the company. Even if they allow for import from US then it's good.
Hi can I have ur contact number...I'm from india
What is the function of chromosome13 in rett syndrome
Rett syndrome is a neurodevelopmental disorder primarily caused by mutations in the MECP2 gene located on chromosome X. Chromosome 13 is not directly implicated in Rett syndrome. The role of chromosome 13 in Rett syndrome is not significant, as the key gene involved, MECP2, is located on chromosome X. However, chromosome 13 and other chromosomes may still indirectly influence various aspects of neurodevelopment and gene regulation, potentially impacting the severity or presentation of Rett syndrome symptoms.
Are you going to do a video on MECP2?
This video is about MeCP2 , click on the youtube video link with this community post
th-cam.com/video/E5RB_Igeu0k/w-d-xo.html This video explains the role of MeCP2