CC BY-NC-ND 4.0 · Indian J Radiol Imaging 2016; 26(01): 70-72
DOI: 10.4103/0971-3026.178336
Obs/Gynec

Prenatal detection of congenital high airway obstruction syndrome with encephalocele

Laxmi Devi Padmanabhan
Division of Perinatology, Amrita Institute of Medical Sciences and Research Centre, Kochi, Kerala, India
,
Sheela Nampoothiri
Department of Paediatric Genetics, Amrita Institute of Medical Sciences and Research Centre, Kochi, Kerala, India
› Author Affiliations
Financial support and sponsorship Nil.

Abstract

Congenital high airway obstruction syndrome (CHAOS) causes secondary morphological changes which can be detected on ultrasound. Here we report a case of congenital high airway obstruction with an occipital encephalocele detected at 23 weeks of gestation.



Publication History

Article published online:
30 July 2021

© 2016. Indian Radiological Association. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial-License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/).

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  • References

  • 1 Online Mendelian Inheritance in Man, OMIM ® . Johns Hopkins University, Baltimore, MD. MIM Number: 607132: 02/02/2009: World Wide Web URL. Available from: http://www.omim.org/. [Last accessed on 2014 May 03].
  • 2 Hedrick MH, Ferro MM, Filly RA, Flake AW, Harrison MR, Adzick NS. Congenital high airway obstruction syndrome (CHAOS): A potential for perinatal intervention. J Pediatr Surg 1994;29:271-4.
  • 3 Lim FY, Crombleholme TM, Hedrick HL, Flake AW, Johnson MP, Howell LJ, et al. Congenital high airway obstruction syndrome: Natural history and management. J Pediatr Surg 2003;38:940-5.
  • 4 Al RA, Guven ES, Akturk Z, Sonmezer M, Yalvac S, Kandemir O. Prenatal diagnosis of isolated laryngeal atresia: Case report and literature review. J Ultrasound Med 2007;26:1243-9.
  • 5 Morrison PJ, Macphail S, Williams D, McCusker G, McKeever P, Wright C, et al. Laryngeal atresia or stenosis presenting assecond-trimester fetal ascites-diagnosis and pathology in three independent cases. Prenat Diagn 1998;18:963-7.
  • 6 Kohl T, Hering R, Bauriedel G, Van de Vondel P, Heep A, Keiner S, et al. Fetoscopic and ultrasound-guided decompression of the fetal trachea in a human fetus with Fraser syndrome and congenital high airway obstruction syndrome (CHAOS) from laryngeal atresia. Ultrasound ObstetGynecol 2006;27:84-8.
  • 7 Kalache KD, Chaoui R, Tennstedt C, Bollmann R. Prenatal diagnosis of laryngeal atresiain two cases of congenital high airway obstruction syndrome (CHAOS). Prenat Diagn 1997;17:577-81.
  • 8 ArtuncUlkumen B, Pala HG, Nese N, Tarhan S, Baytur Y. Prenatal diagnosis of congenital high airway obstruction syndrome: Report of two cases and brief review of the literature. Case Rep Obstet Gynecol 2013;2013:728974.
  • 9 Kalache KD, Masturzo B, Scott RJ, Rodeck CH, Chitty LS. Laryngeal atresia, encephalocele, and limb deformities (LEL): A possible new syndrome. J Med Genet 2001;38:420-2.