Schneider, Holm, Schneider, Michael, Lia, Massimiliano, Grange, Dorothy K., Hadj-Rabia, Smail, Clarke, Angus ![]() ![]() |
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Abstract
X-linked hypohidrotic ectodermal dysplasia (XLHED) is a severe genetic disorder that may be treatable with short-term protein replacement therapy during fetal development. This is currently being investigated in a multicenter clinical trial. Affected fetuses can be identified by the number of tooth germs during a routine ultrasound scan in mid-gestation. To understand the attitudes of female XLHED carriers towards prenatal treatment and ultrasonographic screening of the fetus, we analyzed an earlier and a very recent survey among those women and the actual decisions of potential trial participants. Initial analyses were based on a self-administered survey of 167 female XLHED carriers conducted in 2011. A similar questionnaire was completed 12 years later by 72 female XLHED carriers aged 18-45 years. Subsequently, both the path to diagnosis and further decision-making of the first 33 pregnant women screened for participation in the EDELIFE trial were investigated. Most women diagnosed with XLHED considered this disease as an obstacle to having children: About one third had decided not to have children, another third would monitor their pregnancy using invasive genetic testing. In both surveys, a small number of women stated that they would consider termination of pregnancy depending on the test result. When it came to participating in the clinical trial, 80% were likely to take part (17% moderately likely, 63% very likely). Among the first pregnant women screened for this trial, 48% underwent invasive tests, while 52% relied on non-invasive tooth germ imaging for fetal XLHED diagnosis. One pregnancy with an affected fetus was terminated, another one resulted in a miscarriage, one woman declined to participate in the trial, and 12 women (80%) decided to have the affected fetuses treated. Ultrasound-based screening and prenatal treatment of the fetus are viewed positively by the vast majority of female XLHED carriers. [Abstract copyright: © 2025. The Author(s).]
Item Type: | Article |
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Date Type: | Published Online |
Status: | Published |
Schools: | Schools > Medicine |
Publisher: | BioMed Central |
Date of First Compliant Deposit: | 7 May 2025 |
Date of Acceptance: | 1 April 2025 |
Last Modified: | 07 May 2025 10:15 |
URI: | https://orca.cardiff.ac.uk/id/eprint/178115 |
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