15q11q13 microduplication syndrome
Synonyms: 15q11q13 duplication syndrome | Dup(15)(q11q13) | Trisomy 15q11q13
The 15q11-q13 microduplication (dup15q11-q13) syndrome is characterized by neurobehavioral disorders hypotonia cognitive deficit language delay and seizures. Prevalence is unknown.
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 April 2024
Newly diagnosed with
15q11q13 microduplication syndrome?
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Advocacy Organizations
Dup15q Alliance
We empower individuals living with Dup15q syndrome and other related rare diseases to reach their full potential by advancing breakthrough research and life-changing therapeutic treatments, supporting families affected by Dup15q, and promoting advocacy. Our vision is to cultivate a world where families, clinicians, and advocates enable individuals with Dup15q to thrive.
Kadi Luchsinger
We empower individuals living with dup15q syndrome and other related rare diseases to reach their full potential by advancing breakthrough research and life-changing therapeutic treatments, supporting families affected by dup15q, and promoting advocacy.
Rare Chromosome Disorder Support Group – Unique
Providing support and information to anyone affected by a rare chromosome or gene disorder, their families and the professionals caring for them.
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.