Working towards convergence of the clinical management of differences of sex development/intersex conditions and the human rights framework: A case study.

Autor: Cools, Martine, Verhagen, Emmanuelle, Hoebeke, Piet, Van Hoecke, Eline, Cannoot, Pieter
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Zdroj: Clinical Endocrinology; Nov2024, Vol. 101 Issue 5, p499-506, 8p
Abstrakt: Objective: Medical treatments that aim to modify the appearance of the genitals in children who are born with a difference of sex development/intersex (DSD/I*) condition are highly controversial. Human Rights bodies worldwide have argued that such treatments are conflicting with the child's right of personal autonomy and should be legally restricted to the unique situation where the child's physical health is in danger. Design: We here review the current status of legal initiatives in Europe that have addressed the issue of medical treatments in minors who have a DSD for which they have not been able to give personal informed consent due to their young age. Patients: The management of a 3 years old child who has congenital adrenal hyperplasia (CAH) and grows up with atypical‐looking genitals is discussed. Results: In spite of extensive psychosocial support to the child and family from birth onwards, and good medical control of CAH, the child develops signs of emotional distress, suspected to be attributable to the genital difference. Our discussions include perspectives from the multidisciplinary DSD team caring for the child, a human rights specialist, and an intersex activist. From our discussions, we conclude that with evolving medical care, new ethical and human rights challenges are raised. A truly holistic human rights approach should not only consider physical but also mental health and psychosocial and psychosexual adaptation of the child to the medical condition, when reflecting on the acceptability of medical treatments in minors for which no personal informed consent can be obtained due to their young age. In addition it is paramount to include the meaningful participation of the child in the clinical management at the earliest possible stage. Conclusions: Continued convergence of clinical management and the human rights framework can be realised based on constructive discussions involving all stakeholders, and with the best interest of the child – and adult that they will become ‐ as a common goal. [ABSTRACT FROM AUTHOR]
Databáze: Complementary Index
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