Test Detail

Multi-disease genetic panel for the Fox Terrier grouping three molecular tests for hereditary conditions described in the breed: spinocerebellar ataxia (SCA), primary lens luxation (PLL) and van den Ende-Gupta syndrome (VDEGS). Each condition has its own molecular basis and inheritance. The panel is complementary to ocular and neurological examination in breeding selection.

Applicable breed: Fox Terrier (smooth and wire-haired depending on the condition). Reliable carrier frequencies in the breeding population are not published systematically (limited data); PLL is relatively frequent in small terrier lines.

- Genotype breeding animals before mating; the panel covers three conditions in a single sample\n- For SCA and VDEGS (recessive): do not mate two carriers — 25% risk of affected homozygotes; carrier×clear is safe for offspring intended for breeding if tested\n- For PLL (incomplete dominant): heterozygotes can transmit the variant to 50% of the offspring; prioritise clear animals for breeding and carry out an annual ophthalmological assessment\n- While the SCA and VDEGS genes are being confirmed, avoid mating affected animals and keep a genealogical record of lines with cases\n- After a confirmed clinical case, do not repeat the parental mating and communicate the status to the buyer

SCA must be differentiated from other cerebellar ataxias and from acquired causes (infectious, toxic, neoplastic). PLL must be differentiated from traumatic luxation or luxation secondary to uveitis. VDEGS has a differential diagnosis with other congenital skeletal dysplasias; molecular study confirms it. Annual ocular examination (ECVO/CERF) in all breeding animals. | NOTE 2026-09-18: CHG/TPO in the Fox Terrier with no published cases (limited data).

3. Gould D y cols. ADAMTS17 y luxación primaria de lente (PMID 22050825)