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3q26 microduplication syndrome
rare3q26 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.
- Identifiers
- MONDO:0019878 Orphanet:96095
- Also known as
- Cornelia de Lange-like syndrome · dup(3)(q26) · dup(3q) syndrome · trisomy 3q26
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