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https://rarediseases.info.nih.gov/diseases/1626/currarino-triad
39 rows · Mar 30, 2016 · Currarino triad or syndrome is an autosomal dominant hereditary condition which is characterized by the triad of sacral agenesis abnormalities (abnormally developed lower spine), anorectal malformation (most commonly in the form of anorectal stenosis) and presacral mass consisting of a teratoma, anterior sacral meningocele or both.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4980882/
Currarino syndrome (CS) is a rare clinical condition. The classical presentation includes a triad of sacral anomaly, anorectal malformations, and presacral mass. This syndrome belongs to the group of persistent neuroenteric malformations.
https://yourchiropractichealth.com/currarino-syndrom
Currarino syndrome is a symptomatic triad of anorectal and sacral abnormalities with presacral masses. The syndrome is a hereditary disease that is often associated with a mutation of the MNX1 gene and is caused by a faulty separation of Ento and Neuroektoderm. Causal therapies do not exist.
https://surgicalneurologyint.com/surgicalint-articles/neurosurgical-management-of-currarino-syndrome-a-case-series-and-review-of-literature/
Currarino syndrome (CS) is a rare condition defined by a triad consisting of anorectal malformations, sacral bone deformities, and presacral masses.[2, 7] Approximately 70% of cases are familial with an autosomal dominant inheritance pattern.
https://radiopaedia.org/articles/currarino-syndrome-1?lang=us
The 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...
https://www.medicinenet.com/script/main/art.asp?articlekey=12974
Sep 07, 2018 · Currarino syndrome is a condition characterized by the combination of: Partial absence of the sacrum (the lowest portion of spine), Anorectal (anal and rectal) abnormalities, and; An abnormal mass in front of the sacrum (due to a meningocoele or teratoma).
https://ijponline.biomedcentral.com/articles/10.1186/s13052-018-0500-2
May 25, 2018 · Currarino syndrome (CS) is a rare congenital malformation characterized by the triad: presacral mass, anorectal malformation and sacral dysgenesis. Several incomplete forms of CS with variable phenotypes are described, since the only mandatory clinical feature for CS diagnosis is the sacral anomaly [1].Author: Lucia Cococcioni, Susanna Paccagnini, Elena Pozzi, Luigina Spaccini, Elisa Cattaneo, Serena Redaelli...
https://www.omim.org/entry/176450
The Currarino triad involves the association of partial sacral agenesis with intact first sacral vertebra ('sickle-shaped sacrum'), a presacral mass, and anorectal malformation (Currarino et al., 1981).The specific sacral anomaly is distinct to this syndrome.
http://atlasgeneticsoncology.org/Kprones/CurrarinoID10082.html
Currarino syndrome is a multiple congenital anomalies syndrome characterized by partial agenesis of the sacrum in association with pelvic malformation. Anal atresia and the presence of a pre-sacral mass (teratoma and/or anterior meningocoele) make up the so called Currarino triad.
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