Literature DB >> 20560264

A Turner syndrome case associated with anal atresia, interrupted aortic arch and multicystic dysplastic kidney.

Mehmet Mutlu1, Embiya Dilber, Yakup Aslan, Ayşenur Okten, Osman Oztürk.   

Abstract

Although renal and cardiac malformations are commonly seen in Turner syndrome (TS), anorectal malformations, multicystic dysplastic kidney and interrupted aortic arch are quite rare in TS. A newborn with TS with three quite rare congenital malformations (imperforate anus/anal atresia associated with rectovestibular fistula, interrupted aortic arch, and multicystic dysplastic kidney) is presented.

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Year:  2010        PMID: 20560264

Source DB:  PubMed          Journal:  Turk J Pediatr        ISSN: 0041-4301            Impact factor:   0.552


  1 in total

1.  Interrupted aortic arch with isolated persistent left superior vena cava in patient with Turners syndrome.

Authors:  M Obadah Kattea; Osama A Smettei; Abdulrahman Kattea; Rami M Abazid
Journal:  Avicenna J Med       Date:  2016 Oct-Dec
  1 in total

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