De Morsier`s Syndrome Expressed as Congenital Exotropia
Journal of the Korean Ophthalmological Society
; : 869-874, 1999.
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.
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