1p36 deletion syndrome1p36 deletion syndrome
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What Wikipedia says
1p36 deletion syndrome is a congenital genetic disorder characterized by moderate to severe intellectual disability, delayed growth, hypotonia, seizures, limited speech ability, malformations, hearing and vision impairment, and distinct facial features.
Excerpt from the Wikipedia article “1p36 deletion syndrome”, under the CC BY-SA 4.0 license. Read the article on Wikipedia
Image: Nate.hanson, CC BY-SA 3.0, via Wikimedia Commons.
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