Premium
Familial non‐rcd 1 generalised retinal degeneration in Irish setters
Author(s) -
DjajadiningratLaanen S. C.,
Boevé M. H.,
Stades F. C.,
Oost B. A.
Publication year - 2003
Publication title -
journal of small animal practice
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.7
H-Index - 67
eISSN - 1748-5827
pISSN - 0022-4510
DOI - 10.1111/j.1748-5827.2003.tb00130.x
Subject(s) - medicine , retinal degeneration , pedigree chart , atrophy , retinal , ophthalmology , pathology , genetics , biology , gene
Four Irish setters were diagnosed with bilateral retinal degeneration and cataracts at an age ranging from six to 11 years. In three of these dogs, progressive night blindness was reported from an age of eight to 11 years. In the fourth dog, aged six, no signs of visual impairment had been noticed. In all four dogs, the rod‐cone dysplasia type 1 (rcd1) mutation was excluded as a cause, using an allele‐specific PCR. From their three‐generation pedigrees, a familial relationship was detected in three out of four dogs, which were also related to four additional Irish setter dogs with a history and clinical signs suggestive of late‐onset progressive retinal degeneration. These results suggest the existence of a possibly hereditary, late‐onset, progressive retinal atrophy in the Irish setter breed, that is distinct from rcd1.