PubMed · 1997 · 19 citations · 4 references
MedicineCraniofacial BiologyObstetricsMaternal-fetal MedicineObstetric UltrasoundPrenatal DiagnosisCongenital Craniofacial AnomaliesCongenital DisordersCongenital Head AnomaliesFetal Anatomy AssessmentFetal PathologyPrenatal Craniofacial DevelopmentAutosomal Dominant InheritanceCleidocranial DysplasiaSkull Base AbnormalitiesSkull MorphologySkull OsteologySyndromic Craniofacial Disorders
Cleidocranial dysostosis is an autosomal dominant disorder characterized by absence or hypoplasia of the clavicles, skull abnormalities, and abnormal dentition. The prenatal diagnosis of this condition has been reported once previously in a known high-risk pregnancy. In this report we describe the prenatal findings of cleidocranial dysostosis at 19 weeks' gestation in a woman affected with this disorder but undiagnosed before the fetal scan. This report is unique in the sense that an autosomal dominant condition diagnosed in the fetus led to a similar diagnosis in the mother.
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A gene for cleidocranial dysplasia maps to the short arm of chromosome 6.
George Feldman, Nathaniel H. Robin, L A Brueton et al. · PubMed · 1995 · 48 citations