Syndrome Series: Neurofibromatosis Type 1
The latest installment of my syndrome series! This collection of videos highlights some of the major syndromes that affect the head and neck.
Neurofibromatosis Type 1 is diagnosed based on the observation of 2 or more of the following features: 6 or more cafรฉ au lait macules that are 5 mm or more before puberty, 15mm after puberty, two or more neurofibromas or a plexiform neurofibroma, freckling of the armpit or groin, optic pathway glioma, two or more Lisch nodules of the iris, bony changes associated with the syndrome, or a relative with the syndrome.
This video discusses the genetic, clinical, radiographic, and histopathologic findings of the syndrome.
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The views expressed on this channel are entirely my own and do not represent any organization for which I am employed or a member. The content of this channel is intended for educational use only and not intended to serve as medical advice. If you have a concern about your oral health, please consult your oral healthcare provider for a thorough head and neck examination.
For complimentary biopsy submission kits, speaking requests, and all other inquires, please email: StephenRothOralPathology@gmail.com
Stay Well!
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