Official Journal of the European Society of Gynecology
eISSN 2710-2580
Antenatal features and management of alobar holoprosencephaly: a case study
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European Gynecology & Obstetrics
European Society of Gynecology
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Keywords

alobar, antenatal diagnosis, Holoprosencephaly, Pathologic examination, ultrasound

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How to Cite

Rayhane, J., Salim, Z., Khaoula, S., & Aida, M. (2025). Antenatal features and management of alobar holoprosencephaly: a case study. European Gynecology & Obstetrics, 7(1). https://doi.org/10.53260/EGO.257014

Abstract

Holoprosencephaly (HPE) is a congenital malformation of the brain and face due to incomplete cleavage of the prosencephalon. It affects one in 15,000 to 16,000 births. A 37-year-old patient with a medical history of type 2 diabetes under insulin treatment, and an infection with SARS-CoV-2 at 17 weeks of gestation during this pregnancy was referred to us at 21 weeks gestation following the discovery at the second-trimester ultrasound of an alobar HPE. A multidisciplinary meeting concluded that a termination of pregnancy was necessary given the poor neurological prognosis. Although, HPE is a rare congenital brain malformation. Prenatal ultrasound is the preferred diagnostic tool for detecting the condition and determining the need for pregnancy termination

https://doi.org/10.53260/EGO.257014%20
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References

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Copyright (c) 2025 Jelloul Rayhane, Zangar Salim, Samaali Khaoula, Masmoudi Aida