Septo-optic dysplasia with olfactory tract hypoplasia

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Septo-optic dysplasia with olfactory tract hypoplasia

Copyright © Journal of Pediatric Neurosciences Septo-optic dysplasia with olfactory tract hypoplasia Manuel Ribeiro, Álvaro Machado, and João Soares-Fernandes Department of Neuradiology, Hospital de São Marcos, Braga, Portugal. Department of Neurology, Hospital de São Marcos, Braga, Portugal. Address for Correspondence: Dr. Alvaro Machado, Hospital de São Marcos Largo Carlos Amarante Ap 4200 Br...

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Monocular nystagmus with sectoral optic nerve hypoplasia in a patient with septo-optic dysplasia.

This case depicts an unusual presentation of septo-optic dysplasia. A four-year-old female presented with monocular nystagmus and temporal optic disc pallor in her left eye. Despite a normal sized optic nerve head, magnetic resonance imaging (MRI) showed a hypoplastic intraorbital and intracranial left optic nerve in the absence of a septum pellucidum. She was subsequently diagnosed with septo-...

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Unilateral optic nerve hypoplasia with asymmetric septum: A case report of unilateral septo-optic dysplasia

Septo-optic dysplasia is an uncommon diagnosis comprised in part of a unique composition of congenitalmalformations of the central nervous system. It is defined by three principle findings: optic nerve hypoplasia, absence of the septum pellucidum, and clinical pituitary dysfunction. The syndrome may be associated with various cerebral defects including ectopic posterior pituitary, dysgenesis of...

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Septo-optic Dysplasia

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Septo-optic Dysplasia

The SOD phenotype is highly heterogeneous and diagnosis is made in the presence of at least two of these three features. [5] Only about a third of patients have all three features but patients with any component of the syndrome should be screened for the other features too. The cause of SOD is unknown but viral infections, gestational diabetes, environmental teratogens, vascular or degenerative...

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ژورنال

عنوان ژورنال: Journal of Pediatric Neurosciences

سال: 2009

ISSN: 1817-1745

DOI: 10.4103/1817-1745.49112