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TitelCorneal dystrophy in the Hallermann-Streiff syndrome
Abstract Nr.P06
DoelWe present six patients with typical Hallermann-Streiff syndrome.
ResultatenAll have microphthalmia and were operated for congenital cataract .
Three of the patients developed a severe glaucoma and one patient presented repeated uveal effusions.
Five of our patients have the same pattern of corneal stromal opacities. The opacities are ill defined and bilateral; the stroma between the opacities is clear.
The opacities are observed in two children about age 5 years old.
Follow up of 10 years did not reveal a manifest increase of the lesions.
ConclusieThe authors believe that the corneal stromal dystrophy is a feature of the Hallermann-Streiff syndrome and they would excite ophthalmologists to look for this.
Auteur 1
NaamROULEZ
InitialenFMJ
InstituutHUDERF
StadBrussels
Auteur 2
NaamSCHUIL
InitialenJ
InstituutBartimeus Institute
StadZeist
Auteur 3
NaamMEIRE
InitialenFM
InstituutHUDERF
StadBrussels
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