2008UltrasoundRequires access

Septo-optic Dysplasia (De Morsier Syndrome): Case Report and Discussion

Virginia Lodge, Gerald Mason, M.J. Weston

Open publisher page 1 citations

Abstract

Septo-optic dysplasia (SOD or De Morsier Syndrome) is a rare congenital malformation of the brain which is only occasionally detected in utero. It is usually suspected by the absence of the cavum septum pellucidum (CSP). We report the pre-natal ultrasound and MRI findings in one suspected case and discuss the associated diagnostic dilemmas.

About this research paper

What this paper is about

Septo-optic dysplasia (SOD or De Morsier Syndrome) is a rare congenital malformation of the brain which is only occasionally detected in utero. It is usually suspected by the absence of the cavum septum pellucidum (CSP). We report the pre-natal ultrasound and MRI findings in one suspected case and discuss the associated diagnostic dilemmas.

Why it matters

OpenAlex reports 1 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Septo-optic dysplasia (SOD or De Morsier Syndrome) is a rare congenital malformation of the brain which is only occasionally detected in utero. It is usually suspected by the absence of the cavum septum pellucidum (CSP). We report the pre-natal ultrasound and MRI findings in one suspected case and discuss the associated diagnostic dilemmas.

Key concepts: Medicine, Septum pellucidum, Dysplasia, In utero, Pathology, Radiology, Fetus, Pregnancy

Related papers

Back to paper searchBrowse research topicsOriginal source
Septo-optic Dysplasia (De Morsier Syndrome): Case Report and Discussion — Research Paper | ScholarLens