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The
French Connection
Glaucoma & the Iridocorneal Angle
Glaucoma is characterized by an elevation of intraocular pressure (IOP) which, when sustained, causes intraocular damage resulting in blindness. The elevated intraocular pressure occurs because the fluid cannot leave through the iridocorneal angle. Diagnosis and classification of glaucoma requires measurement of the IOP (tonometry) and examination of the iridocorneal angle (gonioscopy). Neither of these tests is part of a routine screening exam for certification. In this breed, primary glaucoma is associated with narrowed iridocrorneal angles and various degrees of congenital angle malformations varying from mild to severe. Dysplastic pectinate ligaments and subsequent narrowed angles are similar to those described in the Basset and American and English Cocker Spaniels. The occurrence of glaucoma is related to the most severe abnormalities of the pectinate ligaments. The relationship between glaucoma development and the anomaly of the pectinate ligament is not clear. B. Persistent pupillary membranes (PPM) Persistent blood vessel remnants in the anterior chamber of the eye which fail to regress normally during the first three months of life. These strands may bridge from iris to iris, iris to cornea, iris to lens, or form sheets of tissue in the anterior chamber. The last three forms pose the greatest threat to vision and when severe, vision impairment or blindness may occur. C. Cataract A partial or complete opacity of the lens and/or its capsule. In cases where cataracts are complete and affect both eyes, blindness results. The prudent approach is to assume cataracts to be hereditary except in cases known to be associated with trauma, other causes of ocular inflammation, specific metabolic diseases, persistent pupillary membrane, persistent hyaloid or nutritional deficiencies. Cataracts may involve the lens completely (diffuse) or in a localized region. D. Persistent hyperplastic primary vitreous (PHPV)/Persistent hyperplastic tunica vasculosa lentis (PHTVL) Persistent hyperplastic primary vitreous is a congenital defect resulting from abnormalities in the development and regression of the hyaloid artery (the primary vitreous) and the interaction of this blood vessel with the posterior lens capsule/cortex during embryogenesis. This condition is often associated with persistent hyperplastic tunica vasculosa lentis which results from failure of regression of the embryologic vascular network which surrounds the developing lens. In the Bouvier des Flandres, the condition is associated with retinal dysplasia and detachment, optic nerve hypoplasia, lenticonus, cataract and congenital blindness. References 1. ACVO Genetics Committee, 1999 and/or Data from CERF All-Breeds Report, 1991- 1998. 2. Boeve' MH, Stades FC: Glaucoom bij hond en kat. Oversicht en retrospectieve evaluatie van 421 patienten I.Pathobiologischeachtergronden, indeling en raspredisposities. [Glaucoma in dogs and cats. Review and retrospective evaluation of 421 patients I. Pathobiological background, classification and breed predisposition]. Tijdschr Diergeneeskd 110: 219, 1985. 3. van der Linde-Sipman JS: Dysplasia of the pectinate ligament and primary glaucoma in the Bouvier des Flandres dog. Vet Pathol 24: 201, 1987. 4. Van Rensburg IBJ, Petrick S, Van der Lagt J, Smit M: Multiple inherited eye anomalies including persistent hyperplastic tunica vasculosa lentis in the Bouvier des Flandres. Prog Vet Comp Ophthal 2:143, 1992. |
Edited
Monday January 05, 2004 09:14 AM -0500
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