Your browser doesn't support javascript.
loading
De Morsier`s Syndrome Expressed as Congenital Exotropia
Article de Ko | WPRIM | ID: wpr-204463
Bibliothèque responsable: WPRO
ABSTRACT
De Morsier syndrome, or septo-optic dysplasia is a developmental anomaly characterized by unilateral or bilaterral optic nerve hypoplasia, agenesis of septum pellucidum, visual disturbance, and a variable spectrum of disturbed hypothalamic-pituitary function. We experienced a 7-month-old female with de Morsier syndrome whose presenting manifestation was congenital exotropia of right eye, and subsequent evaluation revealed optic nerve hypoplasia of right eye, absence of septum pellucidum, and hypothyroidism.
Sujet(s)
Mots clés
Texte intégral: 1 Indice: WPRIM Sujet Principal: Nerf optique / Septum pellucidum / Exotropie / Dysplasie septo-optique / Hypothyroïdie Limites du sujet: Female / Humans / Infant langue: Ko Texte intégral: Journal of the Korean Ophthalmological Society Année: 1999 Type: Article
Texte intégral: 1 Indice: WPRIM Sujet Principal: Nerf optique / Septum pellucidum / Exotropie / Dysplasie septo-optique / Hypothyroïdie Limites du sujet: Female / Humans / Infant langue: Ko Texte intégral: Journal of the Korean Ophthalmological Society Année: 1999 Type: Article