3q26 microduplication syndrome
Synonyms: Dup(3)(q26) | Dup(3q) syndrome | Trisomy 3q26
3q26 microduplication syndrome is a rare chromosomal anomaly characterized by prenatal and postnatal growth retardation developmental delay intellectual impairment dysmorphic signs and variable combination of congenital anomalies including cardiovascular genitourinary and skeletal anomalies and spectrum of caudal 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 December 2023
Newly diagnosed with
3q26 microduplication syndrome?
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Advocacy Organizations
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.