File:Huntington disease.webm
From WikiLectures
Size of this JPG preview of this WEBM file: 800 × 449 pixels. Other resolutions: 320 × 180 pixels | 640 × 360 pixels | 1,024 × 575 pixels | 1,812 × 1,018 pixels.
Original file (WebM audio/video file, VP9/Opus, length 6 min 32 s, 1,812 × 1,018 pixels, 735 kbps overall)
Summary
| Description |
English: What is Huntington disease? Huntington disease is a type of autosomal dominant disorder involving a triplet repeat of CAG, leading to an abnormal protein that results in neuronal cell death, and various movement and cognitive-related symptoms. This video covers the pathophysiology, as well as major clinical signs and symptoms of Huntington disease.
Sources: First Aid Pathoma Principles and Practice of Medical Genetics. Ch 117. Basal ganglia disorders. |
| Date | |
| Source | open.osmosis.org |
| Author | Osmosis |
Licensing
This file is licensed under the Creative Commons Attribution-Share Alike 4.0 International license.
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- attribution – You must give appropriate credit, provide a link to the license, and indicate if changes were made. You may do so in any reasonable manner, but not in any way that suggests the licensor endorses you or your use.
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File history
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| Date/Time | Thumbnail | Dimensions | User | Comment | |
|---|---|---|---|---|---|
| current | 20:54, 20 September 2016 | 6 min 32 s, 1,812 × 1,018 (34.39 MB) | wikimediacommons>OsmoseIt | User created page with UploadWizard |
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