Request PDF on ResearchGate | On Nov 1, , S. Estefanía and others published Displasia septo-óptica. Septo-optic dysplasia (SOD), (de Morsier syndrome) is a rare congenital malformation syndrome featuring underdevelopment of the optic nerve, pituitary gland. Displasia septo-óptica o síndrome DeMorsier: Presentación de 1 caso y revisión bibliográfica. Rev Cubana Pediatr [online]. , vol, n.4, pp.
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It is best thought of as being part of the holoprosencephaly spectrum see classification system for midline malformations. There is no recognised gender predilection. This association is used to define two forms of the condition 1, The abnormality develops pptica 4 th -6 th weeks of gestation, during early forebrain development. All imaging modalities that can visualize the septum pellucidum ultrasound, CT and MRI will detect its absence in septo-optic dysplasia.
Some additional modality dependent features may also be visible.
Septo-optic dysplasia: case report
In addition to enlarged lateral ventricles with an absent septum pellucidum, CT may demonstrate small optic apparatus best seen with volumetric scanning and coronal reformats and associated small bony optic foramina. The management of SOD requires a multidisciplinary team to assess and treat for hormonal imbalance, vision loss, autism and obesity 9. You can also scroll through stacks with your mouse wheel or the keyboard arrow keys.
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Anoftalmía bilateral por displasia septo-óptica: Síndrome de De Morsier
About Blog Go ad-free. Epidemiology Clinical presentation Pathology Radiographic features Treatment and prognosis History and etymology Differential diagnosis Related articles References Images: Cases and figures Imaging differential diagnosis.
Septo-optic dysplasia associated with cerebral cortical dysplasia cortico-septo-optic dysplasia.
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Case 9 Case 9. Lobar holoprosencephaly Lobar holoprosencephaly. Loading Stack – 0 images remaining.