15q14 microdeletion syndrome
Synonyms: Del(15)(q14) | Monosomy 15q14
15q14 microdeletion syndrome is a recently described syndrome characterized by developmental delay short stature and facial dysmorphism.
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 September 2023.
Newly diagnosed with
15q14 microdeletion syndrome?
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Advocacy Organizations
Africa Save Life International (ASLI)
ASLI’s mission is "Empowering Hope, Transforming Lives: Our Commitment to Rare Diseases" At ASLI, we stand united in our unwavering dedication to improving the lives of individuals and families affected by rare diseases. Our mission is grounded in the belief that every person, regardless of the rarity of their condition, deserves access to support, care and treatment in Uganda.
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.
Syndromes Without A Name (SWAN) Australia
Provide information, support and advocacy to families caring for a child with an undiagnosed or rare genetic condition.
Clinical Trials
For a list of clinical trials in this disease area, please click here.