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hemochromatosis is a genetic defect in iron absorption causing excessive iron deposition in the body.
Please Note: at 7:59: Please Note this is an autosomal recessive not sex linked mutation. Ignore the XY/XX linked mutation. The gene responsible for hereditary haemochromatosis (known as HFE gene) is located on chromosome 6.
Error at 18:30- diagnosis, Labs will show increased ferritin, iron and transferring saturation and a decrease in TIBC.
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We hope you like this video and if you want to join our FREE online course- you can find it below.
We help prepare students studying for the USMLE, COMLEX, NCLEX-RN, NCLEX-PN, PANCE, AANC and ABIM exams.
Our students have a 99% pass rate.
You can get access to watch more video like this?
Click the link below if you are a student studying…
For USMLE Step 1 or 2 CK: ▶▶▶ bit.ly/2Drburf◀◀◀
For NCLEX: ▶▶▶bit.ly/2FRDN3F◀◀◀
For PANCE, AANC, ABIM: ▶▶▶bit.ly/2T7WPGT◀◀◀
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Twitter: / ftplectures
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