BibTex RIS Kaynak Göster

Triple-X syndrome accompanied by Chilaiditi syndrome in preterm infant: a case report

Yıl 2016, Cilt: 3 Sayı: 4, 203 - 5, 15.04.2016

Yusuf Kale Dilek Isik Istemi Celik Ahmet Bas Nihal Demirel

Öz

Chilaiditi syndrome is a variant of the rotation of the colon that gives rise to the interposition of the colon between the right diaphragm and the liver intermittently or constantly. Also, Necrotizing enterocolitis is typically seen in premature infants.

In this report, we presented a female case report accompanied with a 47,XXX karyotype and Chialiditi syndrome and Necrotizing enterocolitis. This association was not reported in any case study.

Our findings suggest that abnormalities of X chromosome may be associated with other anomalies. 

Anahtar Kelimeler

Triple X; chilaiditi syndrome; preterm newborn.

Kaynakça

  • Nielsen J, Wohlert M. Sex chromosome abnormalities found among 34,910 newborn children: Results from a 13-year incidence study in Arhus, Denmark. Birth Defects Orig Artic Ser 1990;26:209-223.
  • Robinson A, Chapelle ADL. Sex chromosome abnormalities. In:Rimoin DL, Connor JM, Pyeritz RE, editors. Emery and Rimoin’s Principles and Practice of Medical Genetics. London: Churchill Living stone; 1996;3:991-992.
  • Jones KL. Smith’s recognizable patterns of human malformation. Recognizable Patternsof Malformation, Chromosomal Abnormality Syndromes. Philadelphia: Elsevier-Saunders Inc; 2006;6:72-73.
  • White JJ, Chavez EP, Souza J. Internal hernia of the transverse colon-Chilaiditi syndrome in a child. J PediatrSurg. 2002;37:802-804.
  • Lin PW, Stoll BJ. Necrotising enterocolitis. Lancet. 2006;368:1271-1283.
  • Hassold TJ, Hall H, Hunt P. The origin of human aneuploidy: Where we have been, where we are going. Hum Mol Genet. 2007;16:203-208.
  • Jacobs PA, Baikie AG, Brown WM, Macgregor TN, Maclean N, Harnden DG. Evidence for the existence of the human “super female.” Lancet. 1959;2:423-425.
  • Jones KL. Smith’s Recognizable patterns of human malformation. Recognizable patterns of malformation, chromosomal abnormality syndromes. Philadelphia: Elsevier-Saunders Inc; 2006;6:72-73.
  • Linden MG, Bender BG, Robinson A. Genetic counseling for sex chromosome abnormalities. Am J Med Genet. 2002;110:3-10.
  • Linden MG, Bender BG, Harmon RJ, Mrazek DA, Robinson A. 47,XXX: What is the prognosis? Pediatrics. 1988;82:619-630.
  • Lin HJ, Ndiforchu F, Patell S. Exstrophy of the cloaca in a 47,XXX child: Review of genitourinary malformations in triple-X patients. Am J MedGenet. 1993;45:761-763.
  • Murrain L, Shanske A. Abstract: Triple X Syndrome Accompanied by Aortic Coarctation. American College of Medical Genetics Annual Meeting, Pheonix, Arizona 2008.
  • Trautner MC, Aladangady N, Maalouf E, Misra D. Jejunal atresia in an infant with triple-X syndrome. J Matern Fetal Neonatal Med. 2004;16:198-200.
  • Chang TY, Tiu CM, Chou YH. Hepatodiaphragmatic interposition of the Intestine (Chilaiditi’s Syndrome). Chin J Radiol. 1999;24:101-105.

Medical Science and Discovery

Yıl 2016, Cilt: 3 Sayı: 4, 203 - 5, 15.04.2016

Yusuf Kale Dilek Isik Istemi Celik Ahmet Bas Nihal Demirel

Öz

Kaynakça

  • Nielsen J, Wohlert M. Sex chromosome abnormalities found among 34,910 newborn children: Results from a 13-year incidence study in Arhus, Denmark. Birth Defects Orig Artic Ser 1990;26:209-223.
  • Robinson A, Chapelle ADL. Sex chromosome abnormalities. In:Rimoin DL, Connor JM, Pyeritz RE, editors. Emery and Rimoin’s Principles and Practice of Medical Genetics. London: Churchill Living stone; 1996;3:991-992.
  • Jones KL. Smith’s recognizable patterns of human malformation. Recognizable Patternsof Malformation, Chromosomal Abnormality Syndromes. Philadelphia: Elsevier-Saunders Inc; 2006;6:72-73.
  • White JJ, Chavez EP, Souza J. Internal hernia of the transverse colon-Chilaiditi syndrome in a child. J PediatrSurg. 2002;37:802-804.
  • Lin PW, Stoll BJ. Necrotising enterocolitis. Lancet. 2006;368:1271-1283.
  • Hassold TJ, Hall H, Hunt P. The origin of human aneuploidy: Where we have been, where we are going. Hum Mol Genet. 2007;16:203-208.
  • Jacobs PA, Baikie AG, Brown WM, Macgregor TN, Maclean N, Harnden DG. Evidence for the existence of the human “super female.” Lancet. 1959;2:423-425.
  • Jones KL. Smith’s Recognizable patterns of human malformation. Recognizable patterns of malformation, chromosomal abnormality syndromes. Philadelphia: Elsevier-Saunders Inc; 2006;6:72-73.
  • Linden MG, Bender BG, Robinson A. Genetic counseling for sex chromosome abnormalities. Am J Med Genet. 2002;110:3-10.
  • Linden MG, Bender BG, Harmon RJ, Mrazek DA, Robinson A. 47,XXX: What is the prognosis? Pediatrics. 1988;82:619-630.
  • Lin HJ, Ndiforchu F, Patell S. Exstrophy of the cloaca in a 47,XXX child: Review of genitourinary malformations in triple-X patients. Am J MedGenet. 1993;45:761-763.
  • Murrain L, Shanske A. Abstract: Triple X Syndrome Accompanied by Aortic Coarctation. American College of Medical Genetics Annual Meeting, Pheonix, Arizona 2008.
  • Trautner MC, Aladangady N, Maalouf E, Misra D. Jejunal atresia in an infant with triple-X syndrome. J Matern Fetal Neonatal Med. 2004;16:198-200.
  • Chang TY, Tiu CM, Chou YH. Hepatodiaphragmatic interposition of the Intestine (Chilaiditi’s Syndrome). Chin J Radiol. 1999;24:101-105.
Toplam 14 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Bölüm Vaka Sunumu
Yazarlar

Yusuf Kale

Dilek Isik Bu kişi benim

Istemi Celik Bu kişi benim

Ahmet Bas

Nihal Demirel

Yayımlanma Tarihi 15 Nisan 2016
Yayımlandığı Sayı Yıl 2016 Cilt: 3 Sayı: 4

Kaynak Göster

APA Kale, Y., Isik, D., Celik, I., Bas, A., vd. (2016). Triple-X syndrome accompanied by Chilaiditi syndrome in preterm infant: a case report. Medical Science and Discovery, 3(4), 203-5. https://doi.org/10.17546/msd.98734
AMA Kale Y, Isik D, Celik I, Bas A, Demirel N. Triple-X syndrome accompanied by Chilaiditi syndrome in preterm infant: a case report. Med Sci Discov. Nisan 2016;3(4):203-5. doi:10.17546/msd.98734
Chicago Kale, Yusuf, Dilek Isik, Istemi Celik, Ahmet Bas, ve Nihal Demirel. “Triple-X Syndrome Accompanied by Chilaiditi Syndrome in Preterm Infant: A Case Report”. Medical Science and Discovery 3, sy. 4 (Nisan 2016): 203-5. https://doi.org/10.17546/msd.98734.
EndNote Kale Y, Isik D, Celik I, Bas A, Demirel N (01 Nisan 2016) Triple-X syndrome accompanied by Chilaiditi syndrome in preterm infant: a case report. Medical Science and Discovery 3 4 203–5.
IEEE Y. Kale, D. Isik, I. Celik, A. Bas, ve N. Demirel, “Triple-X syndrome accompanied by Chilaiditi syndrome in preterm infant: a case report”, Med Sci Discov, c. 3, sy. 4, ss. 203–5, 2016, doi: 10.17546/msd.98734.
ISNAD Kale, Yusuf vd. “Triple-X Syndrome Accompanied by Chilaiditi Syndrome in Preterm Infant: A Case Report”. Medical Science and Discovery 3/4 (Nisan 2016), 203-5. https://doi.org/10.17546/msd.98734.
JAMA Kale Y, Isik D, Celik I, Bas A, Demirel N. Triple-X syndrome accompanied by Chilaiditi syndrome in preterm infant: a case report. Med Sci Discov. 2016;3:203–5.
MLA Kale, Yusuf vd. “Triple-X Syndrome Accompanied by Chilaiditi Syndrome in Preterm Infant: A Case Report”. Medical Science and Discovery, c. 3, sy. 4, 2016, ss. 203-5, doi:10.17546/msd.98734.
Vancouver Kale Y, Isik D, Celik I, Bas A, Demirel N. Triple-X syndrome accompanied by Chilaiditi syndrome in preterm infant: a case report. Med Sci Discov. 2016;3(4):203-5.
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