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Up to: Syndromic disease · Partial deletion of the short arm of chromosome 8
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.
This condition has no sub-types.