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Ocular melanosis in the Cairn Terrier: clinical description and investigation of mode of inheritance
Author(s) -
PetersenJones Simon M.,
Forcier Janice,
Mentzer A. Lexi
Publication year - 2007
Publication title -
veterinary ophthalmology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.594
H-Index - 50
eISSN - 1463-5224
pISSN - 1463-5216
DOI - 10.1111/j.1463-5224.2007.00558.x
Subject(s) - medicine , sclera , ophthalmology , glaucoma , melanosis , fundus (uterus) , iris (biosensor) , pathology , anatomy , melanoma , computer security , cancer research , computer science , biometrics
Objective To describe the clinical features of ocular melanosis in Cairn Terriers. Animal studied One hundred and fourteen Cairn Terriers diagnosed with ocular melanosis. Procedure(s) A complete eye examination was performed on each dog. Four dogs (and two unaffected control dogs) underwent a high frequency ultrasound examination of the anterior segment. The pedigrees of affected dogs were analyzed. Results Forty‐four (38.6%) dogs were male and 67 (58.7%) female; the sex of three dogs (2.6%) was not provided. A four‐stage grading system of the ocular changes was developed. There was a variable age of onset, and the earliest change was a dark‐colored thickening of the iris root. This was followed by the development of episcleral/scleral pigment plaques, release of pigment into the aqueous and deposition in the drainage apparatus, particularly ventrally. Secondary glaucoma developed in the most severely affected dogs. A slow progression of pigmentation in the tapetal fundus was observed and in some dogs pigment on the surface of the optic nerve head was seen. Three dogs developed uveal melanocytic neoplasms. Pedigree analysis suggested a possible autosomal dominant mode of inheritance. Conclusions Ocular melanosis is an inherited, probably autosomal‐dominant condition with a variable age of onset and rate of progression. It results in a thickening and pigmentation of the iris, release of pigmented material into the aqueous, pigment deposition in the sclera/episclera, and to a lesser extent posterior segment pigment deposition. Following extensive pigment deposition in the aqueous drainage pathways it can result in secondary glaucoma.