PC-GG18 : Currarino Syndrome in an Adult Woman: A Case Report
대한산부인과학회 학술발표논문집(2018)
摘要
Currarino syndrome is a rare autosomal dominant hereditary disorder and presents a triad that consists of partial sacral dysgenesis, presacral mass and anorectal malformation. Mutation of a homeobox gene, HLXB9 is the major cause in Currarino syndrome. Its clinical presentations are variable such as imperforate anus at birth, persistent constipation from anorectal stenosis, presacral mass, or acute meningitis. We report a 29-year-old female patient diagnosed with Currarinos triad. The patient visited the gynecologic clinic because of suspected pelvic mass.
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