6p22 microdeletion syndrome
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.
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http: //www.orphadata.org. Data version September 2023.
Newly diagnosed with
6p22 microdeletion syndrome?
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Rare Chromosome Disorder Support Group – Unique
To inform, support and alleviate the isolation of anyone affected by a rare chromosome or single gene disorder and to raise public awareness.
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