Charcot-Marie-Tooth USMLE Mnemonic

Charcot-Marie-Tooth disease is a group of progressive hereditary nerve disorders associated with defective production of proteins in peripheral nerves or myelin. The disease is inherited in an autosomal dominant fashion, and the most common mutation is caused by a duplication of the gene, PMP22. Clinical findings to know about include sensory and motor deficits, and foot deformities including hammer toe, pes cavus (high-arched foot), pes planus (flat foot), and foot drop. Nerve damage and resulting muscle atrophy can lead to an “inverted bottle” or “stork leg” appearance of the lower extremities seen in Charcot-Marie-Tooth patients.
Learn more about Charcot-Marie-Tooth and other neurological disorders with Pixorize’s visual mnemonics for the #USMLE #Step1 and NBME shelf exams.
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[@fhb1997]

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.

[@matthewt9654]

You guys make such great content. Please keep it up! Way more focused and to the point than sketchy path!

[@bi0lizard1]

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

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!

[@beverlypra3224]

Please do more of these: they are simply brilliant!

[@zed3063]

Sketchy can’t continue charging extortionate amounts while there are top quality videos like this for free.

[@queensheba9792]

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!

[@chandanaanup579]

Where were u guys till now ???? This makes remembering so much better and easier Subscribed!

[@DRA_KRISH]

OMG!.there is nothing better than this to learn medicine😍

[@heartcryOD]

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!

[@rubaiatsanjidhossain9855]

Thanks

[@julianocg]

I could not be more clear about it! Congrats!

[@Pixorize]

Thanks for watching!

[@gabriellafrancesca3453]

man I can NEVER remember this particular disorder - this is pure gold.

[@gabriellafrancesca3453]

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

[@gabriellafrancesca3453]

@@michigan1085 I forgot it again 😂

[@mohamedabdelaty4208]

Amazing! Thank you! This channel is promising!

[@Pixorize]

Thanks Mohamed!

[@study.4026]

i just found this now and i really love it ♥

[@SupremeKazi]

such an amazing channel!

[@user-nl5kb3le3p]

WONDERFUL

[@sks2686]

Amazing picture. This way it helps a lot to remember!!!!

[@divyakumar7637]

U guys r awesome... D most underrated vlog... I love dis... Keep goin

[@tracyspampinato_staff-wake4523]

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

[@reenapanicker2493]

YOU ARE AMMMAAAAAAAAAAZING! love it! love it! love it!

[@hameedkhan4022]

Fantastic, really great work

[@samahmed3874]

Great video

[@zeinabsaad6204]

creative!

[@Pixorize]

Thanks Zeinab!

[@amalomer3113]

Helppppfullllllllll thank u💙💙💙💙💙💙🌷🌷🌷🌷

[@Pixorize]

Happy to help!

[@dianadelvalle161]

This is amazing! :D Thank you!

[@DRA_KRISH]

Is there any app available ?

[@Pixorize]

Hi there, we don't have an app at the moment, but our website is mobile compatible and should be accessible from most devices!

[@nunchukgrl2]

Sketchy Path should take some lessons from you Pixorize! Short, the point, HY. Gracias.

[@sreejithmg9101]

thank you...

[@samaralaa2341]

Can't thank you enough 👌

[@Saadia1117]

Wow .. thanks a lot

[@sathvikacharya2585]

I LOVE YOU

[@sathvikacharya2585]

No homo

[@Pixorize]

Thanks Sathvik! We appreciate the feedback :)

[@yourcuteguy9737]

amazing,

[@whatthecatdoing2125]

I have CMT I have type 1A

[@shalom12394]

Wow that's awesome 👍

[@zeynepbasllar9685]

Wow that was great

[@spiracticaldoctor7197]

on fire

[@rubaiatsanjidhossain9855]

Nics story

[@nour5459]

Oh man😂you are amazing :3 keep up tye good work❤

[@Mblmsl]

You're so gooood

[@carolphiri3403]

You are the best✌️😂❤️

[@mashalkhalid3419]

this is perfect 😍😍😍😍😍😍

[@DrAdnan]

I can’t wait for all the eponyms to be phased out in medicine haha

[@Pixorize]

But then no one would watch our videos!

[@DrAdnan]

Pixorize I’d still watch :)

[@mar7956]

Ammmmmmmazing!

[@nourkati5391]

Hello looking for a doctor specialized in this disease please help please

[@dingdong436.]

❤❤

[@rabiakulsum8891]

Raghib Asfak ☺

[@dribrahimaldhaify4469]

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

[@atlas3761]

6:55 :)

[@akthamadams7989]

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

[@conseq6840]

@ I agree!