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Up to: Multiple congenital anomalies/dysmorphic syndrome-intellectual disability · Partial deletion of the long arm of chromosome 8
Chromosome 8q21.11 deletion syndrome
Heterozygous overlapping microdeletions on chromosome 8q21.11 resulting in intellectual disability, facial dysmorphism comprising a round face, ptosis, short philtrum, Cupid's bow and prominent low-set ears, nasal speech and mild finger and toe anomalies.
This condition has no sub-types.