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Turner syndrome surgery

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Akash Daswaney, M.B.B.S[2]

Overview

Overview

Surgery is indicated for craniofacial anomalies, to decrease the risk of aortic dissection and for congenital pterygium colli.

Surgery

Surgery

References

References

  1. Cui X, Cui Y, Shi L, Luan J, Zhou X, Han J (2018). “A basic understanding of Turner syndrome: Incidence, complications, diagnosis, and treatment”. Intractable Rare Dis Res. 7 (4): 223–228. doi:10.5582/irdr.2017.01056. PMC 6290843. PMID 30560013.
  2. Frías JL, Davenport ML, Committee on Genetics and Section on Endocrinology (2003). “Health supervision for children with Turner syndrome”. Pediatrics. 111 (3): 692–702. doi:10.1542/peds.111.3.692. PMID 12612263.
  3. Chaput B, Chavoin JP, Lopez R, Meresse T, Nadon F, Herlin C; et al. (2013). “The “posterior cervical lift”: a new approach to pterygium colli management”. Plast Reconstr Surg Glob Open. 1 (6): e46. doi:10.1097/GOX.0b013e3182a8c597. PMC 4174163. PMID 25289240.


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