6p22 microdeletion syndrome

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Synonyms: Del(6)(p22) | Monosomy 6p22

6p22 microdeletion syndrome is a newly described syndrome associated with a variable clinical phenotype including developmental delay facial dysmorphism short neck and diverse malformations.

Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview. Reference: Access aggregated data from Orphanet at Orphadata. Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version June 2024

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6p22 microdeletion syndrome?

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