16p13.11 microdeletion syndrome

16p13.11 microdeletion syndrome is a recently described syndrome characterized by developmental delay, microcephaly, epilepsy, short stature, facial dysmorphism and behavioral problems.

Cleft upper lip

A gap in the upper lip. This is a congenital defect resulting from nonfusion of tissues of the lip during embryonal development.


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PMID (PMCID)