My cousin had Duchenne and passed away in 2008 from cardiovascular complications. I keep him alive by having his WoW character on my account to this day. I miss him.
Dude that was really well put together! I'm doing an assignment on Duchenne Muscular Dystrophy and your video helped me heaps, you explained it better than wikipedia! Thanks again!
My grandson Joshua has DMD, he is 18yrs old, and l'v read lots of information on the ill ness, but found your vidio to be more intresting and thanks cus I've understood more by watching it, well intresting and put together,
I recently got diagnosed with the same thing, no explanation... made a support group that will hopefully grow fast! Join us and share your story! m.facebook.com/myotoniasupport/
Also note that muscular dystrophy can also occur from a nonsense mutation. Which means that the mother does not have to be a carrier for her child to get muscular dystrophy. My brother has duchenne, and my mother was tested, and is not a carrier. To prove that point further, me, a female was also tested, and I am also not a carrier. Keep that in mind as well :) its also pronounced like (DO SHEN) :P
Thank you, very informative in a short video, I like these kinds of videos. I was able to follow what you were saying, even without understanding it. If this makes sense? Which tells me that you’ve done a very good job.
I have been diagnosed with two types of MD...my son has many of the MD traits - can't run, trips, balance issues, weak core muscles, facial/drools...he was diagnosed with Fragile-X as well. My doctor says that there is a connection between the two: MD+ Fragile X. Have you heard of this? Thank you for your video. It was helpful to me.
I wish they would really stop showing me ads to do with a therapist when it has nothing to do with my muscles and things like that knowing that i was diagnosed with that when I was born. I don't even want to have to discuss any of this for anyone to make out like I had to explain this and having to prove this to people has been going on a lot lately even before. I didn't know I had to keep specifying.
my father ,his brother ,sister and his dad all had and passed from mytonic dystrophy . such a bad life to live with It . I was adopted to stop the gene
How are you now please contact me on WhatsApp 91 9322303271 we got good improvement in muscular dystrophy patients cases with the help of acupressure massage therapy healing process power meditation and Ayurvedic medicine
@@laxmangupta2268 how are you now please contact me on WhatsApp 91 9322303271 we got good improvement in muscular dystrophy patients cases with the help of acupressure massage therapy healing process power meditation
Keypoints- Selfnote: Duchenne : symptomatic around age of 5. X linked recessive. Caused by producing rotten Dystropin which support the membrane. Then membrane damaged and Ca++ leakes inside which causes cell death , apoptosis then tissue necrosis. Patients have increased lordosis, weak abdominal and psoudohypertrophic calves. Walk abnormal and on fingertips. BEKERS MUSCULAR DYSTROPY is less severe form of DUCHENNE M.D. MYOTONIC MUSCULAR DYSTROPY is symptomatic in adults. it is coused by DMPK gene( type 1 CTGx3) and CNBM( Type 2 ) gene in chromosome 19. The problem is muscles cannot relax . These patients can also devolop cataract, Mental retardation and Heart problems. Has a typical face dismorphy( Tense cheeks, alopacia, and in chin)
I study medical science too, its medicine without the patients and dead body parts. we study the science behind the medicine. its geared towards people who go into medical reasearch.
My brother In this Muscle drophy at age of 40 years now. We all family is concerned about him. Such a silnice disease killing your muscle and Other health issue inside and outside. Please suggestion Dear
Hello, My son just turned 8 years old. He has a symptom of the Duchenne types. He is tiptoeing still. He falls very easily. Lately we noticed he is falling more often for no reason. His doctor referred him to Stanford and they're planning to do a DNA (gene) test. Please advise if there is anything else we should do. We are really confused.
So if we have girl embryo that is know as a carrier of DMD , could we return this embryo without the fear she will be developing same symptoms as a boy that sick with Duchenne?
2020 trying to pass RN school, thank you Armando!!!
Am humbled by the facility with which the DMD is explained in a comprehensive language and drawing.
Thank you.
My cousin had Duchenne and passed away in 2008 from cardiovascular complications. I keep him alive by having his WoW character on my account to this day. I miss him.
Dude that was really well put together! I'm doing an assignment on Duchenne Muscular Dystrophy and your video helped me heaps, you explained it better than wikipedia!
Thanks again!
Based on your info on this will a alkaline diet reserve this?
Please tell me about your research assignment.
omg thank u. Ive been on houndred different websites and no one was even close to explain what happnes in the cell but u safed my life! ty :)
Neurology exam tomorrow, and I'm watching all of your videos, they are awesome!! Thank you so much!
one of the best myology vids out here thanks!
My grandson Joshua has DMD, he is 18yrs old, and l'v read lots of information on the ill ness, but found your vidio to be more intresting and thanks cus I've understood more by watching it, well intresting and put together,
Jazakallah khair May Allah bless u with the best for this🤲
Dude you ROCK!!!!!
Nice presentation.
James
Thanks this helped with my project a lot
Thank you for sharing this informative research in such a well laid out style of teaching
2021 prepping for my exams (in the next 10 days)And I will win
Thanks Armando ❤️
Thanks for your video
You are doing a good job
Awesome video! For a minute I felt like I was back in a junior high science class. I’ll be showing this to family and friends when needed. Thanks!
Thank you I have Beckers Muscular Dystrophy and I just learned more
Carlo Basile I have Becker Muscular Dystrophy too
helped me better understand my biology class, thanks!
I Found out just 30 min ago I have MMD thank you this was more than the doctor told me
I recently got diagnosed with the same thing, no explanation... made a support group that will hopefully grow fast! Join us and share your story!
m.facebook.com/myotoniasupport/
the video helped me understand the disease process while studying forr my exam.
شرح مفيد ورائع يوضح مرض ضمور العضلات عند الاطفال
Also note that muscular dystrophy can also occur from a nonsense mutation. Which means that the mother does not have to be a carrier for her child to get muscular dystrophy. My brother has duchenne, and my mother was tested, and is not a carrier. To prove that point further, me, a female was also tested, and I am also not a carrier. Keep that in mind as well :) its also pronounced like (DO SHEN) :P
Duchenne
The only place in the world where they cure all incurable diseases.
ua-cam.com/video/V5NHB7PSFxE/v-deo.html
Yogh se Arram mile sakte hai bas
thanks for uploading, you're a great teacher!
Amazing, where were you when i started nursing school?! :D thank you!
5 star.... Amazing teaching style .. Very very helpful
Very nicely put together. Great job.
you're a great teacher!
Thank you! Great explanation and illustrations.
Thanks for the lecture.
Soo good,clean,clear explanation
very well structured! well done
Nice description
Excellent video! Very detailed.
thank you for making these videos I appreciate it. Is very helpful and you make it so easy to understand with those drawings, cheers from Panamá.
Amazing as usual 👍
Excellent explanation.
Please update your older videos
Thank you for sharing your knowledge. Good vid. Keep them coming!
thank you , my husband has duchenes m.d. very informative
Super lecture thanks and love you sir
No bro, just studying medical science:)
The video was just amazing! Thanks.
Thank you, very informative in a short video, I like these kinds of videos. I was able to follow what you were saying, even without understanding it. If this makes sense? Which tells me that you’ve done a very good job.
I have been diagnosed with two types of MD...my son has many of the MD traits - can't run, trips, balance issues, weak core muscles, facial/drools...he was diagnosed with Fragile-X as well. My doctor says that there is a connection between the two: MD+ Fragile X. Have you heard of this? Thank you for your video. It was helpful to me.
yes X chromosome is the real cause of MD.. what's your sons age now?
WE TREAT MD AYURVEDA TREATMENT AND WE WILL HELP IT OUT SEND DETAILS hispharma@gmail.com or call 9818903387
if people are interested, there are also several forms of dystrophy that arise via problems with protein glycosylation and trafficking
Excellent job!
I wish they would really stop showing me ads to do with a therapist when it has nothing to do with my muscles and things like that knowing that i was diagnosed with that when I was born. I don't even want to have to discuss any of this for anyone to make out like I had to explain this and having to prove this to people
has been going on a lot lately even before. I didn't know I had to keep specifying.
Interesting information ,Thank you .
Amazing video . Thank you
Can you please do a session on transverse myelitis and multiple sclerosis ? Thank you
clear, concise, thank you
Thank you so much it was really very helpful
Thank you so much 😊
Thank you, it was great presentation :)
It was great helpful to do my homework :-)
I love you cilp . This cilp really help me understand DMD
Thank you so much.
*your
Mile Winter hello,im BMD sufferier,add my whats app:+8618983211644 or Facebook:juniorliao1985@gmail.com
Thank you so much for this wonderful video! Really gave me a clear understanding >_
great video, man! thank you so much :]
Great video,v detailed. Thank you
THANK U it‘s helpful , Great work
my father ,his brother ,sister and his dad all had and passed from mytonic dystrophy . such a bad life to live with It . I was adopted to stop the gene
thanks so much.. great help
very gud... helped me a lot..
appreciated 🖤
Really helpful! thanx!
Thank you! really helpful!
I have duchenne muscular dystrophy and I am 13 years old and I am still walking
I am of 18
I can walk but can't run
How are you now please contact me on WhatsApp 91 9322303271 we got good improvement in muscular dystrophy patients cases with the help of acupressure massage therapy healing process power meditation and Ayurvedic medicine
@@laxmangupta2268 how are you now please contact me on WhatsApp 91 9322303271 we got good improvement in muscular dystrophy patients cases with the help of acupressure massage therapy healing process power meditation
Keypoints- Selfnote:
Duchenne : symptomatic around age of 5. X linked recessive. Caused by producing rotten Dystropin which support the membrane. Then membrane damaged and Ca++ leakes inside which causes cell death , apoptosis then tissue necrosis. Patients have increased lordosis, weak abdominal and psoudohypertrophic calves. Walk abnormal and on fingertips. BEKERS MUSCULAR DYSTROPY is less severe form of DUCHENNE M.D. MYOTONIC MUSCULAR DYSTROPY is symptomatic in adults. it is coused by DMPK gene( type 1 CTGx3) and CNBM( Type 2 ) gene in chromosome 19. The problem is muscles cannot relax . These patients can also devolop cataract, Mental retardation and Heart problems. Has a typical face dismorphy( Tense cheeks, alopacia, and in chin)
"psuedo-hypotrophied, i think thats a word" that totally made me laugh
Pseudohypertrophied. Correction
Can you make a video explaining ullrich and bethlem congenital muscular dystrophy?
Very nice.. thank u very much.
it was very helpfull, thanks
2021 n still amazing 🤩
Hey Armundo, where can you get the image for this video? It'd really help me with med school to get it and put it up!!!!!!!!!!
Please update any cure of this disease if any in previous couple of years...
thank you
I study medical science too, its medicine without the patients and dead body parts. we study the science behind the medicine. its geared towards people who go into medical reasearch.
Question, can a patient have becker muscular dystrophy and Atherosclerosis? If so what is the chance of living a long life?
Thank You !
well done !
There aren't just 3 types of muscular dystrophy, there's a plenty of them. Also consider variables that can make much more of them......
Ur life saver thank u
im doing a research paper on muscular dystrophy, would you be able to link to me some sites that you used to get this information?
thanks for that now I understand what it is thank u
What would deletions 31 to 44 mean for What type
For all the amazing help you provide, universities should give you an Honorary Doctorates Degree!
Thank You for this information. #Gratitude #ArtistReach
I have Duchenne Muscular Dystrophy is there any treatment I want help please
Excellent. ...
clear, thank you!
Armando, could you do a video on FSHD muscular dystrophy?
dope video
My brother In this Muscle drophy at age of 40 years now.
We all family is concerned about him.
Such a silnice disease killing your muscle and Other health issue inside and outside.
Please suggestion Dear
thank you so much keep up the goood work...)
Thank you bhaiya
Hello,
My son just turned 8 years old. He has a symptom of the Duchenne types. He is tiptoeing still. He falls very easily. Lately we noticed he is falling more often for no reason.
His doctor referred him to Stanford and they're planning to do a DNA (gene) test.
Please advise if there is anything else we should do. We are really confused.
Dude Dude hello,im BMD sufferier,add my whats app:+8618983211644 or Facebook:juniorliao1985@gmail.com
Thank u sir
myotonic dystrophy is the same as STEINERT disease ??
So if we have girl embryo that is know as a carrier of DMD , could we return this embryo without the fear she will be developing same symptoms as a boy that sick with Duchenne?
Why didn’t you go into detail about BMD? I think that information would have been very helpful instead of generalizing it
how to differentiate muscular dystrophy and muscular atrophy?