Cargando…
Isolated Vaginal Agenesis Associated with Multiple Gastrointestinal Anomalies: A Case Report
More than 50% of infants with esophageal atresia have associated anomalies. We present a case report of a 46XX neonate with long-gap esophageal atresia and tracheoesophageal fistula (EA/TEF), anorectal malformation, bowel duplication and vaginal agenesis. This is an unusual association of abnormalit...
Autores principales: | Angotti, R, Molinaro, F, Bulotta, AL, Ferrara, F, Sica, M, Bindi, E, Messina, M |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
EL-MED-Pub
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4942432/ https://www.ncbi.nlm.nih.gov/pubmed/27433450 http://dx.doi.org/10.21699/jns.v5i3.326 |
Ejemplares similares
-
Herlyn–Werner–Wunderlich syndrome: An “early” onset case report and review of Literature
por: Angotti, R., et al.
Publicado: (2015) -
Congenital Pouch Colon Associated with Anorectal Malformation: A Rare Anomaly of Asian Region – Experience of Kurdish Centre
por: Angotti, Rossella, et al.
Publicado: (2018) -
Association of Duodenal Atresia, Malrotation, and Atrial Septal Defect in a Down-Syndrome Patient
por: Angotti, R, et al.
Publicado: (2016) -
Juvenile granulosa cell tumor of the testis: prenatal diagnosis and prescrotal approach
por: Bulotta, Anna Lavinia, et al.
Publicado: (2012) -
Chromosome 18q-Syndrome and 1p terminal duplication in a patient with bilateral vesico-ureteral reflux: case report and literature revision
por: Brandigi, Elisa, et al.
Publicado: (2013)