16p13.11 microdeletion syndrome
Synonyms: Del(16)(p13.11) | Monosomy 16p13.11
16p13.11 microdeletion syndrome is a recently described syndrome characterized by developmental delay microcephaly epilepsy short stature facial dysmorphism and behavioral problems.
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http: //www.orphadata.org. Data version September 2023.
Newly diagnosed with
16p13.11 microdeletion syndrome?
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