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/
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
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.
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.
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)
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
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?
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.
DMD can take place in several different ways not just by a deletion. There can be a duplication as well causing the phenotype of DMD. You are not pronouncing it corectly. There is no "e" at the end. It is just Duchenne. A lot of your information is incorrect. I hope RN's are not using this for their understandings. I suggest you consult PPMD before making any more videos on MD disorders. Thank you for bringing about awareness of Duchenne.
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
I am a big fan of your videos... I am a little bit worried that some people will understand that at 3:21 the couple will always have this combination meanwhile it is a chance they'll have some of it or even a single one of it... Sometimes all offspring are diseased males or totally healthy ones and so on
Ken Kong these's no male carrier in X-linked genetic disease. Male only has one X in chromosome XY (in contrast to female who has 2 Xs in chromosome XX So either the father is healthy (normal X) or he has the disease (abnormal X in which case, he probably wouldn't live long enough to have children anyway) Female can be a carrier if she has one normal X and one abnormal X chromosome. I hope this helps!
I will never forget the day I came across dr igho channel on RUclips , I will always keep it memorable, thank you doctor for helping me cure my muscle dystrophy & pain completely , and putting a smile on my face , you made me feel more alive like never before , Thank you Dr igho
Sir my diagnosis is going on still but according to my history doctors are saying about mitochondrial myopathy because some of symptoms of this disease is showing in my body. My treatment is going on from AIIMS New Delhi India.
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2020 trying to pass RN school, thank you Armando!!!
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.
Am humbled by the facility with which the DMD is explained in a comprehensive language and drawing.
Thank you.
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.
Neurology exam tomorrow, and I'm watching all of your videos, they are awesome!! Thank you so much!
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 :)
Thanks this helped with my project a lot
Jazakallah khair May Allah bless u with the best for this🤲
one of the best myology vids out here thanks!
Dude you ROCK!!!!!
Nice presentation.
James
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,
2021 prepping for my exams (in the next 10 days)And I will win
Thanks Armando ❤️
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 for sharing this informative research in such a well laid out style of teaching
Thanks for your video
You are doing a good job
helped me better understand my biology class, thanks!
the video helped me understand the disease process while studying forr my exam.
thanks for uploading, you're a great teacher!
شرح مفيد ورائع يوضح مرض ضمور العضلات عند الاطفال
Thank you I have Beckers Muscular Dystrophy and I just learned more
Carlo Basile I have Becker Muscular Dystrophy too
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/
Amazing, where were you when i started nursing school?! :D thank you!
Thank you! Great explanation and illustrations.
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.
5 star.... Amazing teaching style .. Very very helpful
very well structured! well done
Very nicely put together. Great job.
Soo good,clean,clear explanation
Excellent stuff
you're a great teacher!
No bro, just studying medical science:)
Thanks for the lecture.
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
Please update your older videos
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
Amazing as usual 👍
thank you , my husband has duchenes m.d. very informative
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.
if people are interested, there are also several forms of dystrophy that arise via problems with protein glycosylation and trafficking
Excellent video! Very detailed.
Excellent explanation.
Thank you for sharing your knowledge. Good vid. Keep them coming!
The video was just amazing! Thanks.
Nice description
Can you please do a session on transverse myelitis and multiple sclerosis ? Thank you
Thank you so much 😊
Super lecture thanks and love you sir
Interesting information ,Thank you .
Excellent job!
Amazing video . Thank you
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)
Thank you so much for this wonderful video! Really gave me a clear understanding >_
It was great helpful to do my homework :-)
Please update any cure of this disease if any in previous couple of years...
clear, concise, thank you
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
Question, can a patient have becker muscular dystrophy and Atherosclerosis? If so what is the chance of living a long life?
Thank you, it was great presentation :)
THANK U it‘s helpful , Great work
great video, man! thank you so much :]
Thank you so much it was really very helpful
What would deletions 31 to 44 mean for What type
thanks so much.. great help
Can you make a video explaining ullrich and bethlem congenital muscular dystrophy?
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
I have Duchenne Muscular Dystrophy is there any treatment I want help please
Great video,v detailed. Thank you
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
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?
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......
Thank you! really helpful!
Really helpful! thanx!
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?
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.
appreciated 🖤
Wonderful
DMD can take place in several different ways not just by a deletion.
There can be a duplication as well causing the phenotype of DMD.
You are not pronouncing it corectly. There is no "e" at the end. It is just Duchenne. A lot of your information is incorrect.
I hope RN's are not using this for their understandings.
I suggest you consult PPMD before making any more videos on MD disorders.
Thank you for bringing about awareness of Duchenne.
myotonic dystrophy is the same as STEINERT disease ??
very gud... helped me a lot..
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
Very nice.. thank u very much.
2021 n still amazing 🤩
Hi. I am from nepal and I am suffering from Becker muscular distrophy.
Ajay Deula god bless you
It seems me too.. from India.
WE TREAT MD AYURVEDA TREATMENT AND WE WILL HELP IT OUT SEND DETAILS hispharma@gmail.com or call 9818903387
it was very helpfull, thanks
Thank You !
"psuedo-hypotrophied, i think thats a word" that totally made me laugh
Pseudohypertrophied. Correction
thank you
I am a big fan of your videos... I am a little bit worried that some people will understand that at 3:21 the couple will always have this combination meanwhile it is a chance they'll have some of it or even a single one of it... Sometimes all offspring are diseased males or totally healthy ones and so on
Sir I am suffering from mitochondrial myopathy I want to know is any effective treatment of this disease. I am from India.
Read bible please
sir please give me some treatment for this
what if both of them is a carrier? are the the children gonna have DMD?
Ken Kong these's no male carrier in X-linked genetic disease. Male only has one X in chromosome XY (in contrast to female who has 2 Xs in chromosome XX
So either the father is healthy (normal X) or he has the disease (abnormal X in which case, he probably wouldn't live long enough to have children anyway) Female can be a carrier if she has one normal X and one abnormal X chromosome. I hope this helps!
Ur life saver thank u
how to differentiate muscular dystrophy and muscular atrophy?
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!!!!!!!!!!
But with adequate care many men with Duchenne can reach 40i or even more.
Contact doctor Akhigbe for your cure with his herbal medicine
Email him now
thanks for that now I understand what it is thank u
Thank you bhaiya
I will never forget the day I came across dr igho channel on RUclips , I will always keep it memorable, thank you doctor for helping me cure my muscle dystrophy & pain completely , and putting a smile on my face , you made me feel more alive like never before , Thank you Dr igho
ruclips.net/video/PEGmhxAIODQ/видео.html
Sir my diagnosis is going on still but according to my history doctors are saying about mitochondrial myopathy because some of symptoms of this disease is showing in my body. My treatment is going on from AIIMS New Delhi India.
How are you now please contact me on WhatsApp 91 9322303271