Paola Mandich

ORCID: 0000-0003-3123-3512 · 1 paper in corpus
case-report 2011
American journal of medical genetics. Part A ·doi:10.1002/ajmg.a.34031

Currarino syndrome (CS) is an autosomal dominant disorder of embryonic development characterized by the triad of anorectal abnormalities, partial sacral agenesis, and presacral mass. Mutations of the HLXB9 gene have been identified in most …