1p36 deletion syndrome is a rare genetic disorder where a small portion of the short arm of chromosome 1 is deleted. Common symptoms include moderate to severe intellectual disability; slower motor development; dysphagia, or difficulty swallowing; and hypotonia, or weak muscle tone, which usually improves with age. Individuals may also exhibit seizures; vision and hearing problems; dysarthria, or difficulty speaking; and self-harm or other behavioral problems; as well as delayed closure of the fontanelles, or soft spots in the skull. #shorts Find our full video library only on Osmosis: http://osms.it/more. Join over 3 million current & future clinicians who learn by Osmosis, and over 130 universities around the world who partner with us to make medical and health education more engaging and efficient. We have unparalleled tools and materials to prepare you to succeed in school, on board exams, and as a future clinician. Sign up for a free trial at http://osms.it/more. If you're interested in exploring an institutional partnership, visit osmosis.org/educators to request a personalized demo. Follow us on social: Facebook: http://osms.it/facebook Twitter: http://osms.it/twitter Instagram for med: http://osms.it/instagram Instagram for nursing: https://osms.it/ignursing TikTok: https://osms.it/tiktok Linkedin: https://osms.it/linkedin Our Vision: Everyone who cares for someone will learn by Osmosis. Our Mission: To empower the world’s clinicians and caregivers with the best learning experience possible. Learn more here: http://osms.it/mission Medical disclaimer: Knowledge Diffusion Inc (DBA Osmosis) does not provide medical advice. Osmosis and the content available on Osmosis's properties (Osmosis.org, YouTube, and other channels) do not provide a diagnosis or other recommendation for treatment and are not a substitute for the professional judgment of a healthcar