Work

Unveiling the prenatal features of HADDS: A case report and literature review

Year: 2025

Type: article

Abstract: shifted code mutation, which expands the pathogenic gene spectrum of EBF3. Furthermore, we did a retrospective analysis of HADDS patients with a history of pregnancy and childbirth. We emphasized that reduced fetal movement, systematic ultrasound scanning, and fetal MRI might add evidence for prenatal diagnosis. The study is the first to explore prenatal screening for this EBF3 gene-related HADDS and is of great relevance.

Source: Heliyon

DOI: 10.1016/j.heliyon.2024.e41591

Authors: Lina Hu, Dongzhi Li, Li Zhen, Yanan Wang

Institutions: Guangzhou Women and Children Medical Center, Guangzhou Medical University

Language: English

Topic: Fetal and Pediatric Neurological Disorders

Subfield: Pediatrics, Perinatology and Child Health

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: gold

Estimated APC paid: $2,270