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Updated: Jul 16, 2026

Midface Hypoplasia and Cranial Base Morphology in Syndromic Craniosynostosis: A Comparative Analysis Study Using a Predictive Regression Model
Published on: November 4, 2025
Osteocraniostenosis: a further case report documenting the antenatal findings
Audrey Smith1, Sarju Mehta, Philip Bullen
1Departments of Clinical Genetics Fetal Medicine, St Mary's Hospital, Manchester, UK.
Abstract:
Osteocraniostenosis is a rare, lethal skeletal dysplasia with a distinctive phenotype and diagnostic X-ray findings. We present a case of an infant who was antenatally detected to have dysmorphic facial features as early as 22 weeks of gestation. Subsequent postnatal investigations confirmed the diagnosis of osteocraniostenosis. These antenatal findings have not been documented previously. We discuss both the antenatal and postnatal findings of this condition.
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