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.
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