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Septo-Optic Dysplasia

A Neurosonographic Review

Department of Radiology, Loma Linda University Medical Center, Loma Linda, CA

Phil-Ann Tan-Sinn, RDMS, RDCS, RVT

Department of Radiology, Loma Linda University Medical Center, Loma Linda, CA, PSinn{at}ahs.llumc.edu

Septo-optic dysplasia (de Morsier syndrome) is a rare intracranial malformation characterized by the absence of the septum pellucidum with optic disk hypoplasia. Associated clinical symptoms include hypothalamic-pituitary dysfunction and varying degrees of visual impairment. Although the exact etiopathology is unknown, some researchers postulate that septo-optic dysplasia is the result of a vascular disruption sequence, an environmental anomaly, an autosomal-recessive inheritance, or a genetic abnormality. The associated intracranial malformations with septo-optic dysplasia are agenesis of the corpus callosum, schizencephaly, and lobar holoprosencephaly. To detect septo-optic dysplasia and its associated anomalies, sonographers must scan beyond the routine axial views in utero as well as the standard, neonatal axial, coronal, and sagittal views.

Key Words: septo-optic dysplasia • agenesis of corpus callosum • schizencephaly • neurosonography • absent septum pellucidum

Journal of Diagnostic Medical Sonography, Vol. 21, No. 6, 479-486 (2005)
DOI: 10.1177/8756479305282915


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