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Currarino triad

ORPHA1552
Synonym(s) Currarino syndrome
Prevalence 1-9 / 100 000
Inheritance Autosomal dominant
or Not applicable
Age of onset All ages
ICD-10
  • Q87.8
OMIM
UMLS
  • C1531773
MeSH
  • C536221
MedDRA -

Summary

Currarino syndrome (CS) is a rare congenital disease characterized by the triad of anorectal malformations (ARMs) (usually anal stenosis), presacral mass (commonly anterior sacral meningocele (ASM) or teratoma) and sacral anomalies (i.e. total or partial agenesis of the sacrum and coccyx or deformity of the sacral vertebrae).

Expert reviewer(s)

  • Dr Elisabeth ROBERT-GNANSIA

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