Automated Fetal Brain MRI Biometry in Healthy and Pathological Cases

August 16, 2026 Β· Grace Period Β· πŸ› the PIPPI Workshop of MICCAI 2026

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Authors Ema Masterl, Tina Vipotnik Vesnaver, Nejc Šubič, Žiga Špiclin arXiv ID 2608.15692 Category cs.CV: Computer Vision Citations 0 Venue the PIPPI Workshop of MICCAI 2026
Abstract
Automated biometric analysis of fetal brain MRI enables reproducible, observer-independent quantitative assessment, yet existing methods are often restricted to few measurements or evaluated only on healthy cases. We assemble and evaluate an automated biometric analysis pipeline that localizes 22 anatomical landmarks on NeSVoR-reconstructed 3D volumes and derives 11 clinically relevant measurements spanning supratentorial, ventricular, cerebellar, and midline structures. We compare two landmark localization models, H3DE-Net and SCN, on a heterogeneous cohort of 122 acquisitions (both healthy controls and range pathologies). Localization accuracy was assessed with a linear mixed-effects model, agreement with normative growth trajectories with calibrated centile charts, and diagnostic utility with a decision tree classifying VM severity. H3DE-Net achieved significantly lower localization error than SCN across all landmarks (mean 1.36 mm vs. 3.58 mm in HC and 1.90 mm vs. 4.13 mm in PC; p < 0.001), and outperformed a GA-based regression baseline in 7 of 11 measurements. H3DE-Net measurements yielded higher classification AUC in every diagnostic group, with the clearest advantage in separating healthy controls from VM. Decision tree thresholds for ventricular width fell near the clinical 10 mm and 15 mm cut-offs used to define and grade VM.
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