This channel is actually saving me so much time, effort and tears in trying to learn all this. Amazing. On behalf of every medic student who watches this / usual visual learning - THANK YOU. You legit deserve the nobel prize for teaching or something.
You MUST do more and cover more disorders. Don’t steer completely away from more common endocrine disorders. EX: Hasimotos Thyroiditis, Even refreshers on things like diabetes would be helpful. Such a memorable way. Very helpful TY
Please do more of these: they are simply brilliant!
5 лет назад+3
While CMT1 is the most common form of CMT and is indeed caused by an AD mutation of PMP2, other types of CMT follow a different pattern of inheritance: AR (Cx32) / linked to the X chromosome, etc. Amazing video, just wanted to clear that out. Thank you so much!
HAHAHA I'm back a year later for step 2 and completely forgot I ever saw this till I saw my comment - idk what it is about CMT but my brain just rejects it completely
CMT is not always autosomal dominant! All Type 4 instances of CMT are inherited in an autosomal recessive pattern. CMT type 3 is usually recessive, as well. Please do not misinform! Thank you for disseminating about CMT, but please update your info!
For the most part it is inherited in an autosomal dominant manner. Most types are, but be mindful that there are recessive subtypes, and de novo types. I have CMT 1A. We'd say it "runs" in the family, but honestly, the most we can do is wobble!! LOL
The mnemonic is too detailed Simpley CMT IS A HERDITARY MIXED PERPHIRAL SENSORY AND MOTOR POLY NEUROPATHY INVERTED CHAMBAIN BOTTOL LEG SHAPE PERPHRAL MUSCLE WEAKNESS FOOT DROP, PES CAPHES REFLEXES ARE ABSENT AND THEY LOSS TOUCH AND PAIN SENSATION HIGH STEPAGE GAIT THEY LOSS PAIN AND
![Charcot Marie Tooth Disease - Symptoms & NEW Treatments! [2024]](/img/1.gif)
This channel is actually saving me so much time, effort and tears in trying to learn all this. Amazing. On behalf of every medic student who watches this / usual visual learning - THANK YOU. You legit deserve the nobel prize for teaching or something.
You guys make such great content. Please keep it up! Way more focused and to the point than sketchy path!
You MUST do more and cover more disorders. Don’t steer completely away from more common endocrine disorders. EX: Hasimotos Thyroiditis, Even refreshers on things like diabetes would be helpful. Such a memorable way. Very helpful TY
Please do more of these: they are simply brilliant!
While CMT1 is the most common form of CMT and is indeed caused by an AD mutation of PMP2, other types of CMT follow a different pattern of inheritance: AR (Cx32) / linked to the X chromosome, etc.
Amazing video, just wanted to clear that out. Thank you so much!
This was helpful. It was weird at first, but I already know this picture is going to come to me when time to take this exam! Please do more!
Where were u guys till now ???? This makes remembering so much better and easier
Subscribed!
Sketchy can’t continue charging extortionate amounts while there are top quality videos like this for free.
OMG!.there is nothing better than this to learn medicine😍
I could not be more clear about it! Congrats!
Thanks for watching!
man I can NEVER remember this particular disorder - this is pure gold.
HAHAHA I'm back a year later for step 2 and completely forgot I ever saw this till I saw my comment - idk what it is about CMT but my brain just rejects it completely
@@michigan1085 I forgot it again 😂
Amazing picture. This way it helps a lot to remember!!!!
CMT is not always autosomal dominant! All Type 4 instances of CMT are inherited in an autosomal recessive pattern. CMT type 3 is usually recessive, as well. Please do not misinform! Thank you for disseminating about CMT, but please update your info!
Thanks
Amazing! Thank you! This channel is promising!
Thanks Mohamed!
such an amazing channel!
i just found this now and i really love it ♥
U guys r awesome... D most underrated vlog... I love dis... Keep goin
YOU ARE AMMMAAAAAAAAAAZING! love it! love it! love it!
Fantastic, really great work
Great video
This is amazing! :D Thank you!
WONDERFUL
Sketchy Path should take some lessons from you Pixorize! Short, the point, HY. Gracias.
For the most part it is inherited in an autosomal dominant manner. Most types are, but be mindful that there are recessive subtypes, and de novo types. I have CMT 1A. We'd say it "runs" in the family, but honestly, the most we can do is wobble!! LOL
Is there any app available ?
Hi there, we don't have an app at the moment, but our website is mobile compatible and should be accessible from most devices!
Can't thank you enough 👌
You are the best✌️😂❤️
Oh man😂you are amazing :3 keep up tye good work❤
thank you...
Helppppfullllllllll thank u💙💙💙💙💙💙🌷🌷🌷🌷
Happy to help!
Wow .. thanks a lot
creative!
Thanks Zeinab!
Wow that's awesome 👍
Wow that was great
I can’t wait for all the eponyms to be phased out in medicine haha
But then no one would watch our videos!
Pixorize I’d still watch :)
amazing,
this is perfect 😍😍😍😍😍😍
You're so gooood
I LOVE YOU
No homo
Thanks Sathvik! We appreciate the feedback :)
Hello looking for a doctor specialized in this disease please help please
I have CMT I have type 1A
Ammmmmmmazing!
on fire
Nics story
❤❤
Raghib Asfak ☺
The mnemonic is too detailed
Simpley CMT IS
A HERDITARY MIXED PERPHIRAL SENSORY AND MOTOR POLY NEUROPATHY
INVERTED CHAMBAIN BOTTOL LEG SHAPE
PERPHRAL MUSCLE WEAKNESS
FOOT DROP, PES CAPHES
REFLEXES ARE ABSENT AND
THEY LOSS TOUCH AND PAIN SENSATION
HIGH STEPAGE GAIT
THEY LOSS PAIN AND
6:55 :)
I have subscribed to this but please get to the point without so much humor. This video could be a lot shorter
The Great Heisenberg are you kidding? Humor literally kept me watching it
@ I agree!