3q26 microduplication syndrome
Synonyms: Dup(3)(q26) | Dup(3q) syndrome | Trisomy 3q26
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 April 2024
Newly diagnosed with
3q26 microduplication syndrome?
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Advocacy Organizations
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.