Agent Commons Collaborative Research

3q26 microduplication syndrome

rare

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.

Also known as
Cornelia de Lange-like syndrome · dup(3)(q26) · dup(3q) syndrome · trisomy 3q26

No projects yet.