Intersex surgeries are non-lifesaving procedures to change natural variations in genital appearance or reproductive anatomy. These are connected to ideas about gender and sexuality, and what “normal” looks like.

Intersex surgeries often come with serious lifelong emotional and physical consequences, high complication rates, and reduced sexual function. When done without the individual’s informed consent, the United Nations considers these surgeries as human rights violations.

Infant intersex surgeries violate principles of informed consent, bodily autonomy, and self-determination. They may also be prohibited by female genital cutting laws and regulations against forced sterilization. Even still, some doctors claim parental consent is enough to change the appearance or function of an intersex infant’s genitalia, including cosmetic alterations to the clitoris.

Many medical organizations agree that intersex people must be able to make decisions about their bodies, including the American Academy of Family PhysiciansGLMA: Health Professional Advancing LGBTQ Equality, the American Counseling Association, and two state-level medical societies (Massachusetts and Michigan). The US Department of Health and Human Services released a report on Intersex Health Equity condemning medically unnecessary, nonconsensual intersex surgeries.

Below are research papers and further resources to understand the ethics of intersex surgery.

Academic Papers and Resources

Other Articles

Additional References to Cite

Thank you to interACT Board member Elizabeth Reis for providing the following list of additional resources:

Peter Hegarty, Marta Prandelli, Tove Lundberg, Lih-Mei Liao, Sarah Creighton, Katrina Roen, Drawing the Line Between Essential and Nonessential Interventions on Intersex Characteristics With European Health Care Professionals, Review of General Psychology, 10.1177/1089268020963622, (108926802096362), (2020).

Mouriquand, P. D., Gorduza, D. B., Gay, C. L., Meyer-Bahlburg, H. F., Baker, L., Baskin, L. S., . . . El Ghoneimi, A. (2016). Surgery in disorders of sex development (DSD) with a gender issue: If (why), when, and how? Journal of Pediatric Urology, 12(3), 139–149.

Dalke, K., Baratz, A., Greenberg, J.A. (2020). “Protecting Children with Intersex Traits: Legal, Ethical and Human Rights Considerations.” SSRN Scholarly Paper. Rochester, NY: Social Science Research Network, https://papers.ssrn.com/abstract=3626410. Peck, E., & Feder, E. K. (2017). Institutional evils, culpable complicity, and duties to engage in moral repair. Metaphilosophy, 48, 203–226.

Roen, K. (2008). “But we have to do something”: Surgical “correction” of atypical genitalia. Body & Society, 14, 47–66.

Roen, K. (2009). Clinical intervention and embodied subjectivity: Atypically sexed children and their parents. In M. Holmes (Ed.), Critical intersex (pp. 15–40). Ashgate. Roen, K., & Hegarty, P. (2018). Shaping parents, shaping penises: How medical teams frame parents’ decisions in response to hypospadias. British Journal of Health Psychology, 23, 967–981.

Timmermans, S., Yang, A., Gardner, M., Keegan, C. E., Yashar, B. M., Fechner, P. Y., . . . Sandberg, D. E. (2018). Does patient-centered care change genital surgery decisions? The strategic use of clinical uncertainty in disorders of sex development clinics. Journal of Health and Social Behavior, 59, 520–535.