Charcot Marie Tooth Syndrome for USMLE

[@Phewy]

after a lifetime of being told to "Just pick up your feet!" I was so very fortunate to find a Doctor to describe this. Thank you for this video! I felt so uniformed discussing this, its great to have videos like yours to inform myself with :)

[@MockBrainworthy]

Nicely done! Short and concise a nice primer to CMT. Living it every day and always looking for information. Thank you!

[@OriginalFamilyProductions]

I have this condition and this video really help me learn more about it

[@knowpassword]

I have this and i have no idea what youre blathering about..

[@citizencitizen3577]

Wow you explained pathophysilogy very super,? Who will say its connexion (gap junction) problem u didn't mention about that?

[@DF1.j]

I dont know way but im very happy 😂 because i have this since 5 years from now (im17) and i had no idea what is going on with me

[@MsBigBlueHouse]

Some types of CMT don't involve myelin at all. Some CMT types are axonal. Those people have normal velocity but decreased amplitude. Sural Nerve is at the ankle rather than the back of the calf. And there are many more different types than 7. A lot of people with CMT have an elevated CK level. CMT can be late onset. with no symptoms for several decades. Only some types start in childhood. I think you're misrepresented what CMT is.

[@saidnassr9963]

I am sorry but myelin sheath is also produced by the oligodendrocytes in the central nervous system not only by shwann cells in the Peripheral Nervous System

[@puddlesplasher7]

CMT is peripheral disorder tho....so it affects Schwann cells, not oligos. This video poorly explains it. If you look at the genes, like PMP22, that will make it make more sense. PMP22 is the gene involved in the most common type. This dude is pronouncing the disease name wrong. Also, type 1 diseases affects myelin; type 2 affects axons and mitochondria

[@flaminmongrel6955]

​@@puddlesplasher7 there's also CMTX

[@flaminmongrel6955]

it is a PNS disorder so schwan cell makes sense.

[@puddlesplasher7]

@flaminmongrel6955 true true... in the 1X model, it seems like the mutation affects connexin which is under myelin sheath near nodes (its under/at paranodal loops) and holds the myelin to axon

[@michaelstapleton9312]

I have HNPP where can I find an article about the anesthetics?

[@flaminmongrel6955]

Articles aren't the 'go to' for medical knowledge since you will end up at pieces written based on journals which have conflicting findings but NCBI is one good source of research publishes so you can read the conclusion parts there, however you may find it difficult to comprehend if you aren't familiar with medical terminology.

I think i might be Charcot Marie Tooth but not sure.

[@FlowerWhiskers111]

This illness is terrible, I feel pain in my whole body 24/7, but thanks to stem cells Im still alive. Treatment is extremally expensive

[@nellyhoffman6194]

Great video

[@DeeRaman]

Amazing video thank you so much!

[@jenniferyork7804]

Does this mean that patients shouldn’t use a topical Lidocaine cream??

[@hopoptv6071]

I'd like to have Korean subtitles.

[@jacqwerner7919]

the diaphragm is affected. the lungs are smaller on a patient with CMT and the esophagus sometimes has a tendency to close up so at times it can be hard to swallow food and it will get stuck in your esophagus and even liquids will sometimes get stuck the solution to that is to go to a GI doctor have an endoscope done and they can stretch your esophagus open.so when he says there's no respiratory issues that is not true I have been to a lecture with a doctor with a room full of other doctors and that was one thing he's stressed was that the diaphragm it's a muscle and he said it is affected so what this man is saying don't believe him get tested I've been tested for sleep apnea and I have terrible obstructive sleep apnea so that is not true that it does not affect your respiratory system it affects your GI system it affects anything in your body that has a muscle!

[@orlandomontes78]

The AFO's are the worst thing. I have not being able to use them. Way too uncomfortable.

[@TheMrfoxguy]

Singer alan jackson has this

[@MedicinePearl]

Very helpful ❤

[@nourkati5391]

Hello I want to help with this disease please

[@khairobaba6482]

same

[@uzmashah2318]

I have this what type of treatment

[@mortyis]

It is pronounced " SHARK-O MA-REE TOOTH DISEASE"

[@thestudyspot]

mortyis Oh really, thanks for correcting me on that. I must say I really hate those silent T's when they come at the end.

[@mortyis]

No worries. :)

[@ashleywalker3813]

+the study spot blame the French.

[@fernandodanieldiasdaniel9003]

mortyis I am the owner of marie toth puddle diseaseNeed helpI am BrazilianI feel a lot of pain in my whole body.I live Brazil+5512996704541Whatsap

[@annelevenson9829]

Where do we get the disability with the dumbest name 😂

[@leroytorres1979]

What are the examples of the drugs you stated? Dumbify it for the ones whi arent in the knowlege cirlce as you. Thanks. Are they drugs prescribed or street or OTC drugs again thanks

[@deathcommon]

CBD helps. NSAIDs are actually harful, despite being something to take the pain away

[@drstellamaguwudzemd9115]

Thank you

[@marimari-nr4ev]

Hello

[@mohamadshaik3075]

This type problem Mee ..I don't now medicin have or no tell Mee any body .my broblem ,genetic , deseases sottas😥😥

[@marimari-nr4ev]

Sl

[@marimari-nr4ev]

Slm

[@hollyhart1436]

Hi, I think my husband has this, what type of doctor do I take him to to find out for sure?

[@jankuipers7474]

NEUROLOGIST

[@thestudyspot]

Podiatrist may also help

[@hopoptv6071]

I have cmt. I want to study that.

[@fernandodanieldiasdaniel9003]

eu tenho esta doenca queria ajuda

[@DF1.j]

I have this and im 17, shit 😂 i guess i have to live with it, Thanks for the video helped a lot

[@johnjonahjameson9102]

I have that, just a new type 😫

[@williamschutz4982]

I have had this for the last 42 yrs. I am now in so much pain I cannot wait for death.

[@_edoyt]

I’m 17 living with this shit, does it really get that much worse? fuck.

[@dnksdjjs4317]

@@_edoyt IM 14 IM SO SCARED 😭

[@Brandonson80]

Same here buddy.

[@TheRealEricaKelly]

wow i know the pain but not waiting on death😞

[@brittoncromersr9280]

Can any one help me I just got diagnosed with cmt

[@lol-ce1og]

There is no help, brother in cmt. Just live life and accept your disease. I'm 29 and was diagnosed when I was 12 - it was hard for me to accept it until I reached my late 20's. Confidence is all you need - never let it dominate you.

[@itsfunx1608]

@@lol-ce1og bro can i make contact with u..

[@itsfunx1608]

Can u contact me plz

[@cartergomez5390]

Can people take medical marijuana for this?

[@pomdapirouge]

These "animalistic" metaphors for all the visible symptoms of the disease sound terrible to me ...

[@ADIGAMAN]

Hi Ihave also this broplim please any body can help me

[@ADIGAMAN]

hi

[@jroark101]

High arch not ark lol. Thanks for the video

[@wheresmycoffeeineededit3639]

He meant 'arc' it is pronounced similar to 'ark'.

[@johnhalbe6530]

I pretend that I don't have it.

[@kanishka1104]

Please sir tamila vidieo podunga

[@OphiuchiChannel]

Im so scared

[@laurenclarke9096]

Hate my life and always will because of it.

[@toxicpearl3784]

Hey, I have CMT too. I know it's hard to do things like run, climb, and keep up with your friends, but you're unique. Something you probably didn't know though, a lot more people have CMT than you think; 1 in 2,500. Maybe we can keep in touch!

[@laurenclarke9096]

Diamond Gamer yeah! That would be great!

[@toxicpearl3784]

+Lauren Clarke what's ur email? Mine is: [e-mail]

[@nopeynope7378]

No need to get mad, there's still so much worse: being blind for example.

[@PIXELSURPRISE]

Well.... I can’t work a normal job because of my Cmt But I do have a KZbin channel ;)

[@finleymartin5354]

I have cmt

[@nopeynope7378]

me2

[@finnthefuzzymoth1717]

Same

[@michellewashere8545]

There are a few mistakes being taught here. YES! There is pain involved. Yes - the diaphragm can be affected. And there was absolutely no mention of possible deafness. This guy sucks as a teacher.

[@deathcommon]

Everyone has different symptoms with various levels of severity and speed of progression. Personally I've had problems my whole life. Speech and Walking issues as a child. Hearing loss. Loss of smell. Loss of some taste. Very bad hip pain. I'm just glad i learned what was wrong with me at 25.

[@aadufie]

yes, he may have made a few mistakes or omitted somethings but at least he has made the effort of making this video. The least you can do is add information nicely and not be mean about it

[@xxclusive8380]

You suck as a veiwer! Make a better video yourself if youre so amazing.

[@lol-ce1og]

@@aadufie Don't blame him, he's bitter

[@floatingcrispbag7842]

Thanks queen I have severe pain from it glad to see ya called that out lol