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Up to: Partial deletion of the long arm of chromosome 20
Paternal 20q13.2q13.3 microdeletion syndrome
Paternal 20q13.2q13.3 microdeletion syndrome is a recently described syndrome characterized by severe pre- and post-natal growth retardation, microcephaly, intractable feeding difficulties, mild psychomotor retardation, hypotonia and facial dysmorphism.
This condition has no sub-types.