thank you so much for making hematology easy. your channel is really helpful :D by the way dont care about the negative comments because some people never appreciate good things.
You were really good.... And trust me with that ..... Haters are all over so don't mind them .... You are doing awesome 👍🏻👍🏻 keep up good work... Thanks 😁
I am very fair white, redhead, 100% Northern European (23&me) but have thalassemia. I’m from Los Angeles but my ancestors can be traced to Mediterranean areas too. If you have thalassemia I suggest you take a DNA test. It’s very interesting to see where your genes come from.
Maldives (south Asian country) has the highest number of thalassemia carriers. About 18% or little bit more. That means 1 out of every 4 men is a carrier,
If there is a problem in alpha or beta chains, hemotetramers will be formed. They are water insoluble & will precipitate in the RBCs, causing ineffective erythropoiesis. Since a hemoglobinopathy dec.globin --> decreased Hb hence anemia.
Thank you so much I've always had struggles with understanding thalassemia subject but now it's much more easier and Thanks goes to you GREAT CHANNEL Keep it up
- Symptoms of Anemia? - Classification of Thalassemia based on MCV (Mean Corpuscular Volume)? - What does the word mean: thalassemia? - Pattern of Inheritance of Thalassemia? - Hemoglobin consists of what 2 things - Heme consists of what 2 things? - How many globin subunits are there? {2:20} - Of the 2 parts of hemoglobin, what part is the problem for thalassemia? Normal values for HbA (%)? Normal values for HbA2 (%)? Normal values for HbF (%)? If the problem is in the alpha subunit, what kind of thalassemia? If the problem is in the beta subunit, what kind of thalassemia? What is formed in thalassemia (defect in alpha or beta globin subunits), and what is their effect on RBCs? {3:28}
Hemotetramers will be formed - will precipitate in RBCs coz water insoluble Globin chains decreased -> Hemoglobin decreased, hence anemia, will lead to ineffective erythropoiesis
I have thalassemia but I'm African American. None of my other siblings have it. I'm not Asian, middle eastern or African. Maybe my ancestors are from somewhere around the Mediterranean.
Thank you so much for your comment. I am so sorry to hear about your condition. I truly wish you best of luck. Yeah, may be ancestors from that area. **This is just for educational purposes only, I am not an expert on these issues** Thanks again!
Now I'm not a genius in any way 😂 but my doctor explained it to me like thalassemia and sickle cell anemia are pretty much the same thing. Sickle cell is the name when black people have it and thalassemia is when white people have it. I'm not sure how true it is though. I have it too
That’s simply NOT TRUE! Sickle cell anemia and thalassemia are different diseases...Yes, they both cause hemolysis, but that doesn’t mean they are the same. Look up their genetics and you will see the difference! Thanks!
@@MedicosisPerfectionalis thanks, it's all good. I'm a silent carrier, which means I'm perfectly healthy i.e. I have one gene. It takes 3 genes to have the actual disease :)
Thanks a lot for this video, I am from Afghanistan. I did my HB electrophoresis after watching your videos. My test results are like this: HBA1 92.9% HBA2 5.5% Fetal HB 1.6 % So how do you interpret this whether I am thalassemia trait carrier/minor or not?
Thanks for your honest feedback, please play the video on 1.5x or 2x...These videos were recorded when I was getting started, I am trying to improve every day! Thanks!
► 💊Antibiotics Lectures: www.medicosisperfectionalis.com/products/courses/antibiotics/
What is HBA2 test why it is done for? Thanks
I actually appreciate the slow voice 😂❤️ thank you you are saving my medical career!
My pleasure 😇
Thanks for watching!
Can you please help me by sharing?
Sure would love to!!
@@lolahpearl6679 hey where are you...
@@arvindsingh3669 🤫
I can't Thank You enough Sir. You got everything that I need for Hematology.
Excellent 👍
I actully find, this slow voice is good .It gives us time to think and summarised as well so no need to give extra time on the topic.
Ok 👍
Every year of exam is incomplete without ur videos....thank u so much for fantastic lectures.....😊
You’re very welcome, Hari 😊
Thank you so much for watching!
😀😀
😊😊
I'm egyptian following you
Thanks for your effort❤️
after watching so many videos about thalassemia....finally i understood.....appriciate ur hardwork🙂
Thank you doctur ... I am grateful to you❤
Thank you!
I put you tube search- thalassemia.
You tube suggestions- thalassemia major?
Me- thalassemia medicosis.
I love your channel
Thank you somuch!!
Thank you so much!
I am honored!
Would you please help me by sharing?
@@MedicosisPerfectionalis yes I did :-)
I don't know why I feel you are Egyptian😂. Your way of explaining is brilliant, just like the Egyptians.🖤🤍❤
Was recently told I have thalassemia, this was a good break down for the type of learning process that I have!
Thank you 🙏
Best of luck!
Thanks a lot!!
thank you so much for making hematology easy. your channel is really helpful :D
by the way dont care about the negative comments because some people never appreciate good things.
You were really good.... And trust me with that ..... Haters are all over so don't mind them .... You are doing awesome 👍🏻👍🏻 keep up good work... Thanks 😁
Thank you so much 😊
I am very fair white, redhead, 100% Northern European (23&me) but have thalassemia. I’m from Los Angeles but my ancestors can be traced to Mediterranean areas too. If you have thalassemia I suggest you take a DNA test. It’s very interesting to see where your genes come from.
Maldives (south Asian country) has the highest number of thalassemia carriers. About 18% or little bit more. That means 1 out of every 4 men is a carrier,
📝 Download my handwritten notes: www.medicosisperfectionalis.com/
Im in your channel from yesterday interesting in your greatful explaining… keep going 🎉👏
Thank you 😊
Thank u so much for ur lectures.. Finally found a teacher with non - stinging voice.. 😂 ❤️
Sir you are helping us to understand better..
Thank you 😊
Plz don't drunk during giving lectures😂😂😂😂
😅 I am not
Ahaha
i knew it.. :D
Ikr 😂
Yeah actually 😂😂
It helpful in neet
Thxx sir
thank you thank you thank you, u saved my life, god bless you
God bless you too!
❤️ Cardiac Pharmacology Course: www.medicosisperfectionalis.com/
📝 Download my Notes: www.medicosisperfectionalis.com/
Watching from India
Welcome 🙏
You are amazing !! Explained it well ❤️
Thank you so much!
If there is a problem in alpha or beta chains, hemotetramers will be formed. They are water insoluble & will precipitate in the RBCs, causing ineffective erythropoiesis.
Since a hemoglobinopathy dec.globin --> decreased Hb hence anemia.
Thank you so much
I've always had struggles with understanding thalassemia subject but now it's much more easier and Thanks goes to you
GREAT CHANNEL
Keep it up
Thanks a ton! Good luck 👍
Doppest general knowledge eva🔥🔥🔥
Thank you so much!
I love hematology bc of u thank bro 💜💜
My pleasure!
Thanks alot jazakallah ❤️❤️
My pleasure!
🩸 Hematology Playlist: ruclips.net/p/PLYcLrRDaR8_eoNz6dxXolh1XMEietcniU&si=tomFsUjAgOKhOJVq
I love your voice 😍🥺❤️
Thank you!
- Symptoms of Anemia?
- Classification of Thalassemia based on MCV (Mean Corpuscular Volume)?
- What does the word mean: thalassemia?
- Pattern of Inheritance of Thalassemia?
- Hemoglobin consists of what 2 things
- Heme consists of what 2 things?
- How many globin subunits are there? {2:20}
- Of the 2 parts of hemoglobin, what part is the problem for thalassemia?
Normal values for HbA (%)?
Normal values for HbA2 (%)?
Normal values for HbF (%)?
If the problem is in the alpha subunit, what kind of thalassemia?
If the problem is in the beta subunit, what kind of thalassemia?
What is formed in thalassemia (defect in alpha or beta globin subunits), and what is their effect on RBCs? {3:28}
Hemotetramers will be formed
- will precipitate in RBCs coz water insoluble
Globin chains decreased -> Hemoglobin decreased, hence anemia, will lead to ineffective erythropoiesis
Thank you, you-save my life
You are grrrrrreeeaaaattttt my lovely teacher❤
Thank you 😊
thank you doctor
My pleasure!
Thank you so much you are amazing
I appreciate you!
Very very helpful thank you very much to your efforts ,,from iraq..
You are so welcome!
عظييييم 💜💋
Feeling sleepy with your speaking style😂BTW,awesome video
Thank you ☺️
Great speed. You took your medication beforehand.
Thank you so much for these videos sir ✨
Thank you so much! 9/6/2019 😁
You’re always welcome 🙏
Medicosis when u make jokes you sound just like Damon Salvatore...and i love you medicosis...plz reveal your face😁♥️
I appeared 👻 in a few videos!
awesome lecture sir 🤩
Thank you 😊
I like your vedioes so much ,some one recommended Osmosis channel for me but you are the best.
By the way, what is your name Mr.medicosis???
You can call me “Medicosis”.
Thank you for making this 👍👍
My pleasure 😇
I have thalassemia but I'm African American. None of my other siblings have it. I'm not Asian, middle eastern or African.
Maybe my ancestors are from somewhere around the Mediterranean.
Thank you so much for your comment.
I am so sorry to hear about your condition.
I truly wish you best of luck.
Yeah, may be ancestors from that area.
**This is just for educational purposes only, I am not an expert on these issues**
Thanks again!
Now I'm not a genius in any way 😂 but my doctor explained it to me like thalassemia and sickle cell anemia are pretty much the same thing. Sickle cell is the name when black people have it and thalassemia is when white people have it. I'm not sure how true it is though. I have it too
That’s simply NOT TRUE! Sickle cell anemia and thalassemia are different diseases...Yes, they both cause hemolysis, but that doesn’t mean they are the same. Look up their genetics and you will see the difference! Thanks!
Medicosis Perfectionalis Thanks for correcting that!
Of course...Thank you for asking!
explain excellent❤️ I have thalassemia 🥺
Thanks 🙏
I am so sorry to hear that!
How is your health today?
Medicosis Perfectionalis thanks 😍 I’m fine ❤️❤️
thank you so much!!!!💕💕💕
You’re always welcome 🙏
Thanks from California!
You’re welcome 😊
Name. % Normal values%
Hb A 70.2 >=97.8
Hb E 26.1
Hb A2 3.7 2.2 - 3.2
comment: Suggestive of Hb trait
please help me.
my wife pregnancy 9 month running
Please talk to your doctor!
Thankyou so much sir
You have very informative video but when I try to watch when am tired i definitely fall sleep 😂
:)
Very helpful
Thanks a lot
+Malak Hamadto You are always welcome!
Can thalassemia person and g6pd person give birth and have a healthy child? Or is there a high risk of getting a unhealthy ones?
thank you
You’re welcome!
l am alpha thalassemia carrier and my partner is beta thalassemia carrier ,what is affect to my children?
Awesome👍
Thanks!
Tq
Welcome!
Are you photographer ?
Amateur level.
can you make a video on sickle cell anemia pls
Sure! It is coming soon...
Sickle Cell Disease “Part 1” Intro ruclips.net/video/mhWlEJ741ME/видео.html
Medicosis Perfectionalis thank you so much
You’re so welcome:)
I swear I thought that I had accidentally set up the playback speed at 0.75 x
Listening in 1.75 and still thinking... Well... pretty normal.
do u have any video for pedigree?
Yes, I have a few Genetics videos in my Biology playlist.
I just found out today that I'm an alpha silent carrier, hence checking out this vid lol!
I am so sorry to hear that!
Best of luck!
@@MedicosisPerfectionalis thanks, it's all good. I'm a silent carrier, which means I'm perfectly healthy i.e. I have one gene. It takes 3 genes to have the actual disease :)
@@stoneroses3493 best of luck was for the child, that hope he/she isn't affected by Thalassemia
@@bionicpenguin5471 my husband isn't a carrier, so all good :)
if both carriers get married and have 2 children. which child is have the possibility of getting a Thalassemia major?the first on or the second one?
Is thalassemia is genetic disease or suddenly disorder
What do you mean by suddenly?
@@MedicosisPerfectionalis i can affect people age of 30 or someother age bt their parents are normal
Amazing
Thanks, dear:)
Thanks a lot for this video, I am from Afghanistan. I did my HB electrophoresis after watching your videos.
My test results are like this:
HBA1 92.9%
HBA2 5.5%
Fetal HB 1.6 %
So how do you interpret this whether I am thalassemia trait carrier/minor or not?
Thanks for reply
B thalassemia trait?
Why the face in ur videos makes me a little bit nervous??😶
What do you think? 🤔
Just kidding... btw your videos are awesome.Keep making videos with relevant cases pls.
😂😂 sure
May be the face’s eyes 👀 were piercing through your soul 😂
Yeah😅😅
I LOVE YOU
I LOVE YOU
I LOVE YOU
I LOVE YOU
I LOVE YOU
I LOVE YOU 💕
Thank you so much!
Sir I need source for this which book did you mentioned this
I use Goljan, Harrison’s and Davidson’s
i couldn't listen over 30"... that hangover voice.
Is anyone there? Please help me is thalassemia and thalassaemia the same? Or not?
Same, it’s American vs British spelling.
Speed : 1.25x 🙃
Fair enough
Too slow
Good info.. But don't be drunk
Are u Arabian? 🥰
Yes
@@MedicosisPerfectionalisWallah Greeeeeeat🥰, I knew that from your accent!
You sound tired .
😞
@@MedicosisPerfectionalis it's okay man
U speak tooo slowly 😔 otherwise vedios are good
Thanks for your honest feedback, please play the video on 1.5x or 2x...These videos were recorded when I was getting started, I am trying to improve every day! Thanks!
@@MedicosisPerfectionalis I guess every student is different because I actually appreciated the pace of this video as a first-time learner.
You sound so sleepy
I know
Too much slow video bro😠😠😠😠
Fair enough
dont you think you are thalasemia patient😂😂
???
@@MedicosisPerfectionalis dont worry just kidding because of your slow voice😂
Ganja
why are u drunk😐
I am not.
Dont drunk yarr whats this sounds quality
u drunk bro?
I think you’re high
Nope!
Why are you talking like that bye 😭😭😭
boring
dood you are sounding so cringe don't drink then talk it sounds so weird!