1. Introduction
Intersex variations represent a natural expression of human bodily diversity. Their existence places intersex individuals in a position of vulnerability within social and medical systems historically designed around a dichotomous model of sex. Within this framework, the present study is part of a broader effort to examine whether healthcare professionals’ beliefs, attitudes, and levels of knowledge influence the clinical practices applied to intersex individuals, and whether such practices may be shaped, beyond strictly medical criteria, by conformity to and identification with gender stereotypes and normative gender roles (Garland et al., 2022 [
1]).
Medical History and the Normative Construction of Intersex Bodies
Intersexuality refers to a range of biological conditions in which an individual is born with sex characteristics that do not fit typical definitions of male or female. These differences may occur at the chromosomal, gonadal, hormonal, or morphological level. The binary sex system has proven insufficient to encompass this diversity, leading to processes of invisibilization, pathologization, and stigmatization of intersex bodies (Karkazis, 2008 [
2]; Fausto-Sterling, 2021 [
3]).
Historically, medicine has interpreted intersexuality through a corrective lens, grounded in the normalization of the body within a binary framework. Until the 1950s, intersex variations were primarily understood through a pathological perspective, and early taxonomies were deeply rooted in the establishment of morphological criteria for classifying intersex individuals (Karkazis, 2008 [
2]). From the mid-twentieth century onward, the prevailing model was based on the belief that gender identity was malleable and could be shaped through medical intervention and socialization (Kessler, 1990 [
4]). This view legitimized early surgical and hormonal interventions, often performed without proper informed consent from the patient or their legal guardians (Tovar, 2013 [
5]), with the aim of aligning intersex bodies to a dichotomous sexual model that would facilitate social integration according to hegemonic standards.
Since then, this model has been widely criticized for failing to capture the complexity of intersex experiences and for disregarding the serious physical and psychological consequences of interventions intended to “correct” bodily variations to fit social norms. Such practices have been questioned not only for their long-term health and psychological impacts (Minto et al., 2003 [
6]; Garland et al., 2022 [
1]), but also for being grounded more in sociocultural constructs than in scientific evidence (Fausto-Sterling, 2021 [
3]; Bonavia & Palacios Pérez, 2020 [
7]).
The conceptualization of intersex embodiment as a “disorder” has hindered essential legal and social progress (Lauroba, 2018 [
8]), contributing to the stigmatization and invisibility of intersex individuals. The motivations behind medical interventions have been, and often continue to be, centered on normative social participation, with their perceived necessity driven more by social anxieties than by scientific evidence. In fact, such interventions can result in severe lifelong physical and psychological consequences (Garland et al., 2022 [
1]). Clinical decision-making has frequently prioritized conformity to social expectations of what a “male” or “female” body should be.
Although it may seem striking, several authors have documented how traditional medical protocols included immediate diagnosis upon the presence of ambiguous genitalia, followed by gender assignment based on criteria such as penile size, the ability to urinate while standing, or vaginal penetrability (Hernández Guanche, 2009 [
9]). These practices, now the subject of growing ethical and scientific criticism, were primarily focused on surgical “normalization” and reproductive or coital criteria rather than on the well-being of the patient. They reflected prevailing social norms and anxieties related to gender and sexuality, with little scientific grounding and weak clinical justification (Garland et al., 2022 [
1]; Bonavia & Palacios Pérez, 2020 [
7]; Haghighat et al., 2023 [
10]). Consequently, medical treatments of intersexuality have historically prioritized gender conformity over the autonomy and holistic well-being of intersex individuals (Minto et al., 2003 [
6]).
From the Corrective Model to Epistemological Critique: Questioning the Dominant Clinical Paradigm
Medical practice has long operated under the assumption that gender assignment, reinforced through early surgical intervention, would promote psychosocial well-being in adulthood. However, this premise lacks solid empirical support. Relevant studies (Minto et al., 2003 [
6]; Garland et al., 2022 [
1]) indicate that there is no conclusive evidence that early surgeries improve long-term psychological or social adjustment, nor that they ensure the development of a gender identity consistent with the initial assignment. Far from demonstrating unequivocal benefits, genital interventions can entail significant risks, such as the loss of sexual function resulting from the removal of clitoral or phallic tissue (Minto et al., 2003 [
6]). Given the absence of evidence showing that such procedures yield better outcomes than allowing bodily development without surgical modification, it is reasonable to question whether their true purpose lies not in preventing future suffering, but in aligning bodies with a normative ideal.
The sex–gender binary system, rather than accommodating existing bodily diversity, has proven insufficient to capture the complexity of human experience. Instead of recognizing the natural spectrum of bodies, it imposes rigid categories that pathologize what does not conform to them (Fausto-Sterling, 2021 [
3]). This imposition reveals a corrective rather than a therapeutic logic.
Within this context, various theoretical perspectives, such as Butler’s (2007) [
11] work and queer pedagogies (Sánchez Sáinz, 2019 [
12]), have called for a critical reassessment of the epistemological foundations underlying medical practice. The challenge is not merely to reform clinical protocols, but to re-examine, and perhaps reconfigure, the very lens through which medicine has historically approached bodily and gender diversity.
Consequences of Pathologization: Health, Consent, and Human Rights Violations
The pathologization of sexual variations has hindered progress toward a culture of acceptance and respect for diversity. These circumstances are exacerbated when healthcare professionals operate under deterministic personal beliefs or an uncritical identification with gender stereotypes, which can lead to perceiving intersex bodies as problems to be “fixed” rather than as legitimate expressions of human diversity (Platero, 2012 [
13]). This context calls into question the validity of informed consent, as families may be influenced by social pressures or receive incomplete information, limiting their ability to make fully informed and autonomous decisions.
In many cases, decisions are made before the child has the opportunity to express their own will, thereby violating fundamental principles such as progressive autonomy and the free development of personality (Camacho Gutiérrez, 2016 [
14]; Tovar, 2013 [
5]). Several studies indicate that families often make medical decisions without fully understanding their implications, partly because the information provided is insufficient, biased, or presented as the only possible course of action (Bonavia & Palacios Pérez, 2020 [
7]; Haghighat et al., 2023 [
10]). The consequences of the aforementioned protocols and practices extend beyond physical development, affecting the subjective construction of identity and the mental health of intersex individuals. Reports of body shame, difficulties in accessing adequate healthcare, and social rejection among those who have undergone “normalization” procedures point to a structural problem that transcends the strictly medical domain (Minto et al., 2003 [
6]; Leivas et al., 2023 [
15]). Early corrective surgeries can also result in sexual dysfunction, loss of genital sensitivity, body rejection, and psychological disorders (Minto et al., 2003 [
6]).
In this regard, several studies have documented that intersex women who underwent clitoral surgery exhibit significantly higher rates of non-sensuality (78%) and inability to achieve orgasm (39%) compared with those who were not surgically treated (20% and 0%, respectively) (Minto et al., 2003 [
6]).
Legal Progress and International Recognition of Intersex Rights
In response to this situation, several legal frameworks have been developed to prohibit medically unnecessary interventions and to safeguard the physical integrity of intersex individuals (ILGA World, 2023 [
16]). The United Nations has taken steps to recognize and protect the rights of intersex people, condemning non-consensual surgical interventions and other invasive treatments performed on intersex infants and children. Malta was the first European country to ban such practices in April 2015, setting a legal precedent that was later followed by others. Iceland, for example, prohibited intersex genital mutilation on July 19, 2021. In Spain, the Law 4/2023 for the Real and Effective Equality of Trans and LGBTI People introduced a specific provision banning non-consensual genital modifications in intersex minors under the age of 12, except in cases where such interventions are medically necessary to protect the individual’s health. These laws aim to protect the rights of intersex people (Lauroba, 2018 [
8]) and prevent unnecessary surgical procedures lacking medical justification. However, the legal situation continues to vary significantly across countries, and in many regions, such practices remain unregulated or legally permissible. At the same time, intersex rights movements in Latin America and the Caribbean have gained increasing visibility, successfully positioning intersex issues on both international and national policy agendas. This growing advocacy has contributed to a broader recognition of the need to deconstruct traditional binary notions of “male” and “female” within legal, medical, and social frameworks.
Gaps in Medical Training
In recent years, increasing attention has been drawn to the idea that medical decisions concerning intersex individuals may stem more from a lack of information and from social or cultural imperatives than from objective clinical needs. As a result, new clinical guidelines have been developed that explicitly prohibit non-essential surgical interventions. However, little research has explored in depth how healthcare professionals’ beliefs about intersexuality, and the presence, or absence, of related content in medical education influence decision-making in everyday clinical practice. Existing literature has largely focused on the effects of medical interventions on patients and on advocating for their prohibition when not medically necessary, while paying less attention to the critical examination of the epistemological and normative frameworks that underlie these clinical decisions. In some cases, such frameworks may continue to legitimize interventions perceived as necessary, despite lacking true medical justification.
This study aims to address this gap by empirically examining those factors.
Toward a Critical Medicine: The Need to Transform the Care Model
The guiding hypothesis of this study stems from a critical premise: what is deemed clinically appropriate may be deeply influenced by personal beliefs and by a cultural framework that equates legitimacy with conformity to a binary ideal of sex and gender. In light of a model historically oriented toward morphological conformity to the binary ideal, it becomes urgent to question its underlying assumptions, as well as clinical approaches that disregard children’s progressive autonomy and fail to recognize bodily diversity as a legitimate human reality (Camacho Gutiérrez, 2016 [
14]; Suess & Abiétar, 2021 [
17]).
This research therefore aims to provide empirical evidence to advance toward a more ethical, informed, and respectful clinical model, one that transforms professional training practices, challenges stereotypes, and acknowledges that medicine itself is embedded within normative social systems. Only through a critical revision of these structural frameworks will it be possible to ensure respect for the rights of intersex individuals and to build a truly inclusive model of healthcare.