Disorders of Fatty Acid Oxidation (2 of 3)

[@anthonycheung4425]

These are wonderful videos, great for med students trying to figure out biochemical genetics!

[@jesiraj2448]

Thank you Dr. Boone for this excellent overview. God bless you. Please upload more medical genetics lectures, an excellent learning resourse for us.

[@Zumbador]

Easy to follow and good transition with Part One. It's really a very good review of the basics to build upon for Inborn Errors of Metabolism. Thanks again. On to Part 3...

[@maaggiied2554]

I have LCHAD and was diagnosed a few months after birth. I doctor identified it as a FAOD and sent a tissue sample to Australia and it took 6 weeks for results. I’m 21 and still the only one in New Zealand with LCHAD. NBS wasn’t available to diagnosed LCHAD until I was 7

[@andreabarbeau9351]

My daughter has vlcad. Great informative video. Thank you for posting.

[@AmineTutobioch]

Thanks so much for the clear explanation

[@samirbrahimi5782]

Great work sir 😁 keep us updated plz

[@cultivatedincreativity]

My son has SCADD and was in ketosis. You are saying here that NOT having ketones is a clue for FOD. My son also has hyperammonia and "autism"

[@Theultrazombiekiller]

I have CPT2 deficiency. Not diagnoses until 25 years old.

[@chetanchetan23]

great video .THANKS

[@ummelailamirza8968]

Thanks 🙏