Great lecture sir. One correction, cystic fibrosis is a monogenic disorder. involving a single gene which codes for the protein CFTR. What you are talking about is deletion of three nucleotides which codes for phenylalanine, the most common of all mutations- F508 del. there are in fact more than 1500 mutations causing cystic fibrosis.
Thank you your video. I am a Respiratory Therapist who been out of the field for a few years and now have my first grandbaby diagnosed with CF from the baby screening that was done after she was born. Your video is a great refresher and I am wanting to learn as much as I can. When it is your own it is a little different with your own. Your brain does not remember everything that I learned in college or on the job.
They thought my niece was going to be sick from this because both parents are CF carriers but my niece is healthy, she is turning 10 soon and hardly ever gets sick from anything.🙏🏼
No mention of ivacaftor agent which reverses abnormality in chloride channels used in G551D defect cystic fibrosis . One of the best explanation of cystic fibrosis .
a great brother of dr najeeb both are just gem of med school Met you at seminar imperial college bahria town Seminar or stroke rehab great description given there by Dr been still refreshing my concepts about there
Don't you mean three bases are deleted instead of 3 genes? There is only a single CFTR gene. The phenylalanine is the 508th amino acid that is deleted, but not 3 whole genes...
Great lecture. Question though, isn’t it most often that males are infertile due to congenital agenesis of the vas deferens in CF and not due to thick secretions?
It is great explanation on the pathophysiology aspect. ON the treatments part, there is also a new approach of CFTR correctors/modulators that you didn't mention. These drugs improve/modulate the CFTR chloride channel performances. Few products approved by FDA and being used by health care community are Symdeko (FDA approved February 2018), Ivacaftor ...
However could you please detail about the channels which are working differently in sweat glands and respiratory system.? Detail as in more precisely the mechanism and effects. Would be grateful !
Good explanation, just wanted to clarify at @1:30 that 3 genes are not deleted bur rather within the cftr gene a single nucleotide codon that sequences the amino acid phenylalanine is deleted thus leading to some conformational changes in the translated protein
Hi anyone plz help me out from this Iam having a symptoms for past 1yrs that include wheezing (only when black or brownish sputum comes out),middle of chest pain,sputum with black or brownish color (@that time alone cough) and iam an NON SMOKER 20yrs old . I have consulted 2 pulmonologist and ENT but nothing works ...kindly help me 😔😔🙏
Sir....i had a doubt...the expired air is considered to be more warm than the air inspired.The reason stated is with the physiological heat of our RT and water vapours. Can u explain from where did water vapours originate???
![Jack Harlow - Hello Miss Johnson [Official Music Video]](http://i.ytimg.com/vi/Q86_nlRoIGw/mqdefault.jpg)
this is by far the best explanation in whole youtube on CF...
Great lecture sir. One correction, cystic fibrosis is a monogenic disorder. involving a single gene which codes for the protein CFTR. What you are talking about is deletion of three nucleotides which codes for phenylalanine, the most common of all mutations- F508 del. there are in fact more than 1500 mutations causing cystic fibrosis.
Medicine and reading textbooks are truly difficult unless someone like you start to teach it with all of his efforts
Thank you your video. I am a Respiratory Therapist who been out of the field for a few years and now have my first grandbaby diagnosed with CF from the baby screening that was done after she was born.
Your video is a great refresher and I am wanting to learn as much as I can. When it is your own it is a little different with your own. Your brain does not remember everything that I learned in college or on the job.
It's you only sir, who is able to make me understand the pathophysiology of CF in my medical carrier of 17 years.
Thank you sir.
Best lecture ! Cleared out my confusions regarding different mechanisms in sweat gland and digestive secretions! Great explanation Sir!
They thought my niece was going to be sick from this because both parents are CF carriers but my niece is healthy, she is turning 10 soon and hardly ever gets sick from anything.🙏🏼
Good for her. Praying that she always stays healthy, prosperous, and happy.
Please make more videos Sir
We need more teachers like you!!
Thank u. Its my first lecture.It is awesome..first time i got the real story behind cystic fibrosis ✌
You are most welcome. Glad the lecture is valuable.
Such a detailed explanation with easy understanding... Best lecture I have heard ever about CF. Thank you Sir.
THANK YOU ! THIS IS THE BEST VIDEO FOR CF
No mention of ivacaftor agent which reverses abnormality in chloride channels used in G551D defect cystic fibrosis .
One of the best explanation of cystic fibrosis .
Easiest and concept based understanding , thank you sir 🙏♥️
No word for your lacture sir.. thanks and make more video for us ...
extremely thankful for a very important lecture.
First time, I got the answer of my question of salty sweat basis.
Hats Off to the lecturer
Thanks a lot... sir...your explanation skill is too much good...sir..🙏
You are very welcome!
As usual your the best sir it's great lecture.
Thank you dear. Check drbeen.com for more lectures. #Drbeen
a great brother of dr najeeb both are just gem of med school Met you at seminar imperial college bahria town Seminar or stroke rehab great description given there by Dr been still refreshing my concepts about there
Well explained
Really good lectures
At the end of lecture plz repeat all points again 🙏🙏tnx
amazing video sir...i wish i had came across this video before.
really and simply superb sir
Great explanation Sir...
Don't you mean three bases are deleted instead of 3 genes? There is only a single CFTR gene. The phenylalanine is the 508th amino acid that is deleted, but not 3 whole genes...
Thank you very much , god bless you 💕💕
You are very welcome
Great lecture. Question though, isn’t it most often that males are infertile due to congenital agenesis of the vas deferens in CF and not due to thick secretions?
excellent. Thank you so much Sir..
It is great explanation on the pathophysiology aspect. ON the treatments part, there is also a new approach of CFTR correctors/modulators that you didn't mention. These drugs improve/modulate the CFTR chloride channel performances. Few products approved by FDA and being used by health care community are Symdeko (FDA approved February 2018), Ivacaftor ...
absolutely brilliant and logical. thank you dr!
Thank you dr been the best of all cystic fibrosis you are special
good efforts sir
Awesome sir. Love your lecture
Thank you dear 😍
thank you from algeria
Simple, short and brilliant
Thank you sir :)
However could you please detail about the channels which are working differently in sweat glands and respiratory system.? Detail as in more precisely the mechanism and effects.
Would be grateful !
Great lecture, thank you!
Pleasure. Check drbeen.com for more lectures.
thank you sir good lecture.........
amazing! thannkss
excellent presentatiomDr.been.thanks
Thank you dear.
Very good explain sir
Its very helpfull thank you❤️❤️❤️
Glad to know that. You are welcome!
wonderful Dr. Mubeen, Thanks :)
Thank you
Good explanation, just wanted to clarify at @1:30 that 3 genes are not deleted bur rather within the cftr gene a single nucleotide codon that sequences the amino acid phenylalanine is deleted thus leading to some conformational changes in the translated protein
Ammmaaazzziiinnng! Thanks a lot!
One doubt Sir, chloride ions in respiratory tract where do they ultimately go? Reabsorped or secreted?
Thank you sooo much
Thanks sir plz give us some lectures on biochemistry or biophysics
can u explain the genetic cause of cistic fibrosis
Will do.
Great lecture sir
Thank you!
Wholesome video
Thank you!
Hi anyone plz help me out from this Iam having a symptoms for past 1yrs that include wheezing (only when black or brownish sputum comes out),middle of chest pain,sputum with black or brownish color (@that time alone cough) and iam an NON SMOKER 20yrs old . I have consulted 2 pulmonologist and ENT but nothing works ...kindly help me 😔😔🙏
excellent
Thank.you.so.much.sir.
Sir there is a problem with cftr channel (chlorine channel) so chlorine won't be absorbed but why sodium channel won't work to absorb again
thanks sir
Sir....i had a doubt...the expired air is considered to be more warm than the air inspired.The reason stated is with the physiological heat of our RT and water vapours. Can u explain from where did water vapours originate???
Water vapors come from the moist airways. Water is part of the airway secretions.
They are water molecules originated from the surface of the respiratory epithelium, when a dry air is passing across the respiratory passage
Sir I have a question, if CFTR Cl- is not present at all. How come Chlorid Ions get inside the cell?
thank you , amaaaaazing
Great...👍
thanks ALOOOOOT
me indiya me rheti hu mere bete ko cystic fibrosis hai me kya kru??? kucch ilaj btaye koi docter btaye plz plz
I am also from india and my daughter also has CF. She also has bronchiectasis....
cool one👍
my child is "salty" when i kiss him hahahha. great lecture btw! thankyou!
I love you
"Please pay attention". Lol. That can be your phrase. All my professors have their own phrase.
Great explanation
That was awesome sir, thanks alot.