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Megacystis microcolon intestinal hypoperistalsis syndrome in a newborn

Year 2019, Volume: 44 Issue: 1, 276 - 278, 31.03.2019
https://doi.org/10.17826/cumj.442232

Abstract

References

  • 1.White SM, Chamberlain P, Hitchcock R, Sullivan PB, Boyd PA. Megacystis-microcolon-intestinal hypoperistalsis syndrome: the difficulties with antenatal diagnosis. Case report and review of the literatüre. Prenat Diagn. 2000;20:697-700.
  • 2.De Sousa J, Upadhyay V, Stone P. Megacystis Microcolon Intestinal Hypoperistalsis Syndrome: Case Reports and Discussion of the Literature. Fetal Diagn Ther. 2016;39:152-7.
  • 3.Berdon WE, Baker DH, Blanc WA, Gay B, Santulli TV, Donavan C. Megacystis-microcolon-intestinal hypoperistalsis syndrome: a new cause of intestinal obstruction in newborn. Re port of radiologic findings in five newborn girls. Am J Roentgenol. 1976;126:957-964.
  • 4.Young ID, McKeever PA, Brown LA, Lang GD. Prenatal diagnosis of the megacystis-microcolon-intestinal hypoperistalsis syndrome. J Med Genet. 1989;26:403-406.
  • 5. Wymer KM, Anderson BB, Wilkens AA, Gundeti MS. Megacystis microcolon intestinal hypoperistalsis syndrome: Case series and updated review of the literature with an emphasis on urologic management. J Pediatr Surg. 2016 ;51:1565-73.
  • 6.Buinoiu N, Panaitescu A, Demetrian M, Ionescu S, Peltecu G, Veduta A. Ultrasound prenatal diagnosis of typical megacystis, microcolon, intestinal hypoperistalsis syndrome. Clin Case Rep. 2018;6:855-858.
  • 7.Moreno CA, Sobreira N, Pugh E, Zhang P, Steel G, Torres FR, et al. Homozygous deletion in MYL9 expands the molecular basis of megacystis-microcolon-intestinal hypoperistalsis syndrome. Eur J Hum Genet. 2018;26:669-675.

Bir yenidoğanda megasistis mikrokolon intestinal hipoperistaltizm sendromu

Year 2019, Volume: 44 Issue: 1, 276 - 278, 31.03.2019
https://doi.org/10.17826/cumj.442232

Abstract

-

References

  • 1.White SM, Chamberlain P, Hitchcock R, Sullivan PB, Boyd PA. Megacystis-microcolon-intestinal hypoperistalsis syndrome: the difficulties with antenatal diagnosis. Case report and review of the literatüre. Prenat Diagn. 2000;20:697-700.
  • 2.De Sousa J, Upadhyay V, Stone P. Megacystis Microcolon Intestinal Hypoperistalsis Syndrome: Case Reports and Discussion of the Literature. Fetal Diagn Ther. 2016;39:152-7.
  • 3.Berdon WE, Baker DH, Blanc WA, Gay B, Santulli TV, Donavan C. Megacystis-microcolon-intestinal hypoperistalsis syndrome: a new cause of intestinal obstruction in newborn. Re port of radiologic findings in five newborn girls. Am J Roentgenol. 1976;126:957-964.
  • 4.Young ID, McKeever PA, Brown LA, Lang GD. Prenatal diagnosis of the megacystis-microcolon-intestinal hypoperistalsis syndrome. J Med Genet. 1989;26:403-406.
  • 5. Wymer KM, Anderson BB, Wilkens AA, Gundeti MS. Megacystis microcolon intestinal hypoperistalsis syndrome: Case series and updated review of the literature with an emphasis on urologic management. J Pediatr Surg. 2016 ;51:1565-73.
  • 6.Buinoiu N, Panaitescu A, Demetrian M, Ionescu S, Peltecu G, Veduta A. Ultrasound prenatal diagnosis of typical megacystis, microcolon, intestinal hypoperistalsis syndrome. Clin Case Rep. 2018;6:855-858.
  • 7.Moreno CA, Sobreira N, Pugh E, Zhang P, Steel G, Torres FR, et al. Homozygous deletion in MYL9 expands the molecular basis of megacystis-microcolon-intestinal hypoperistalsis syndrome. Eur J Hum Genet. 2018;26:669-675.
There are 7 citations in total.

Details

Primary Language Turkish
Subjects Health Care Administration
Journal Section Letter to the Editor
Authors

Perihan Eşsizoğlu 0000-0002-3452-8634

Ferda Özlü 0000-0002-2092-8426

Hüseyin Şimşek This is me 0000-0002-3453-6802

Hacer Yapıcıoğlu This is me 0000-0001-6295-553X

Mehmet Satar 0000-0002-5718-0503

Önder Özden This is me 0000-0001-5683-204X

Publication Date March 31, 2019
Acceptance Date July 10, 2018
Published in Issue Year 2019 Volume: 44 Issue: 1

Cite

MLA Eşsizoğlu, Perihan et al. “Bir yenidoğanda Megasistis Mikrokolon Intestinal Hipoperistaltizm Sendromu”. Cukurova Medical Journal, vol. 44, no. 1, 2019, pp. 276-8, doi:10.17826/cumj.442232.