Collie eye anomaly in the Lancashire heeler
1Department of Small Animal Medicine and Surgery, Royal Veterinary College, Hatfield, Hertfordshire.
The Veterinary Record
|November 4, 1998
Summary
Collie eye anomaly (CEA) is now identified in Lancashire heelers, affecting 13.7% of the surveyed population. This suggests CEA is a single genetic trait, not separate conditions, and may require a new name.
Area of Science:
- Veterinary Ophthalmology
- Canine Genetics
Background:
- Collie eye anomaly (CEA) is a known inherited ocular condition.
- The condition has traditionally been associated with Collie breeds.
Purpose of the Study:
- To describe an ocular disease in Lancashire heelers that is clinically identical to Collie eye anomaly (CEA).
- To investigate the genetic basis and nomenclature of this condition in a non-Collie breed.
Main Methods:
- Ophthalmoscopic examination of Lancashire heelers.
- Pedigree analysis to assess inheritance patterns.
- Literature review on Collie eye anomaly (CEA).
Main Results:
- An ocular disease identical to CEA was identified in Lancashire heelers with a 13.7% incidence in a 1996 survey.
- Clinical findings and pedigree data support CEA as a single, recessively inherited Mendelian trait.
- The presence of CEA in a non-Collie breed suggests the current nomenclature is inappropriate.
Conclusions:
- The ocular disease observed in Lancashire heelers is ophthalmoscopically identical to Collie eye anomaly (CEA).
- Evidence supports CEA as a single pleiomorphic trait segregating as a recessive Mendelian trait.
- The term 'congenital posterior segment anomaly' is proposed as a more appropriate name for the condition.
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