Congenital diaphragmatic hernia other diagnostic studies

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Congenital diaphragmatic hernia Microchapters

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Arooj Naz, M.B.B.S

Overview

Diagnostic studied that can be utilized include high resolution ultrasound, chorionic villus sampling, amniocentesis, microarray analysis, and karyotyping. Although these studies are not necessarily diagnostic for CDH, they help identify underlying genetic defects which have a high correlation rate with diaphragmatic hernia's.

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References

  1. https://www.cdc.gov/ncbddd/birthdefects/diagnosis.html. Missing or empty |title= (help)
  2. Shemilt L, Verbanis E, Schwenke J, Estandarte AK, Xiong G, Harder R; et al. (2015). "Karyotyping human chromosomes by optical and X-ray ptychography methods". Biophys J. 108 (3): 706–13. doi:10.1016/j.bpj.2014.11.3456. PMC 4317545. PMID 25650937.