10q22.3q23.3 microduplication syndrome
Synonyms: Dup(10)(q22.3q23.3) | Trisomy 10q22.3q23.3
A rare chromosomal anomaly characterized by variable clinical features that may include developmental delay mild intellectual disability and dysmorphic facial features. In some cases microcephaly growth retardation and congenital heart defects have been reported.
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
10q22.3q23.3 microduplication syndrome?
Our RARE Concierge Services Guides are available to assist you by providing information, resources and connections as you navigate your rare disease journey.
Advocacy Organizations
17q12 Foundation
Creating a community for those affected by 17q12 syndromes while raising awareness and encouraging research.
Malaysian Rare Disorders Society
1. Provide support to individuals and families affected with Rare Disorders. 2. Develop strategies and programs to raise public and professional 3. Ensure Human Rights of access to healthcare education, job opportunities are upheld. 4. Participate in the formulation and implementation national policies in Malaysia related to person with rare disorders and rare disorders
Petronille Healthy Society
Petronille Healthy Society is committed to providing free healthcare services, education, and training to communities in need, especially the most vulnerable and underserved populations.
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.
Youth And Women for Opportunities Uganda-YWOU
Our mission supports Rare, orphan and undiagnosed diseases diagnosis, care and treatment, education, awareness and empowering health care professionals and patients care takers of rare, orphan and undiagnosed diseases arena in Uganda, build capacity and bridge lack of clinical knowledge and experience and provide search/quest for diagnostic laboratories, I advocate for changes in laws, practices
ZTTK SON-Shine Foundation
To aid, connect, support, advocate, raise awareness, promote research and education about ZTTK Syndrome for patients and families
Clinical Trials
For a list of clinical trials in this disease area, please click here.