3q26 microduplication syndrome

MONDO:0019878

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

0 clinical trials for this condition and its sub-types, 0 tagged with 3q26 microduplication syndrome itself.

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Part of

↑ Partial duplication of the long arm of chromosome 3 (1)

Including sub-types (0) Tagged with 3q26 microduplication syndrome (0)

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