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Bookmark or Share- Currarino syndrome - OrphanetA rare developmental defect during embryogenesis characterized by the triad of anorectal malformations, presacral mass and sacral anomalies. Estimated prevalence is 1-9/100,000. Recent data estimates a 1.39:1 female-to-male ratio.
- Currarino syndrome - WikipediaCurrarino syndrome is an inherited congenital disorder where either the sacrum (the fused vertebrae forming the back of the pelvis) is not formed properly, or there is a mass in the presacral space in front of the sacrum, and there are malformations of the anus or rectum. It occurs in approximately 1 in 100,000 people.
- Currarino syndrome | Radiology Reference Article - Radiopaedia.orgThe Currarino syndrome is a complex condition variably comprised of characteristic congenital anomalies of the sacrum, anorectum and presacral soft tissues. It is also known as the Currarino triad or ASP triad, however, not all three features are always present 6.
- Currarino syndrome: a comprehensive genetic review of a rare ... - PubMedBackground: The triad of a presacral mass, sacral agenesis and an anorectal anomaly constitutes the rare Currarino syndrome (CS), which is caused by dorsal-ventral patterning defects during embryonic development. The major causative CS gene is MNX1, encoding a homeobox protein.
- Currarino syndrome: a comprehensive genetic review of a rare congenital ...The triad of a presacral mass, sacral agenesis and an anorectal anomaly constitutes the rare Currarino syndrome (CS), which is caused by dorsal–ventral patterning defects during embryonic development. The major causative CS gene is MNX1, encoding a homeobox protein.
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