RECTAL DUPLICATION CYST IN PREVIOUS ANORECTAL MALFORMATION AND DOWN SYNDROME | Zendy

A. Burgio | Zendy; Francesco Ferrara | Zendy; E. Cerchia | Zendy; E. Brandigi | Zendy; Rossella Angotti | Zendy; Francesco Molinaro | Zendy; Mario Messina | Zendy

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RECTAL DUPLICATION CYST IN PREVIOUS ANORECTAL MALFORMATION AND DOWN SYNDROME

Author(s) -

A. Burgio,

Francesco Ferrara,

E. Cerchia,

E. Brandigi,

Rossella Angotti,

Francesco Molinaro,

Mario Messina

Publication year - 2012

Publication title -

journal of the siena academy of sciences

Language(s) - English

Resource type - Journals

eISSN - 2279-882X

pISSN - 2279-8811

DOI - 10.4081/jsas.2012.57.2

Subject(s) - rectum , gene duplication , medicine , constipation , cyst , gastrointestinal tract , ileum , anatomy , surgery , biology , genetics , gene

Gastrointestinal (GI) tract duplications are rare congenital malformations. Most of them occur in the ileum and only 1-5%, of all duplication, were in the rectum. Different clinical features including chronic constipation, rectal prolapsed or polips. We report on a 4-years-old girl with Down syndrome and anorectal malformation (ARM) who was found to have a rectal duplication cyst

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