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8p23.1 microdeletion syndrome
8p23.1 deletion involves a partial deletion of the short arm of chromosome 8 characterized by low birth weight, postnatal growth deficiency, mild intellectual deficit, hyperactivity, craniofacial abnormalities, and congenital heart defects.
Thin vermilion border
Reduced width of the skin of vermilion border region of upper lip.
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PMID (PMCID)