Test Detail

Pack 1 Cavalier King Charles Spaniel: episodic falling (EF) + dry eye curly coat syndrome (CCS)

General · Dog

Breed genetic panel for the Cavalier King Charles Spaniel grouping two well-characterised recessive hereditary conditions: « episodic falling » (EF, hypertonic episodes induced by exercise/emotion) and « dry eye curly coat » syndrome (CCS, congenital keratoconjunctivitis sicca + curly coat + ichthyosis/scaling + flaking). Both have been associated with different variants and often co-segregate in the breed, so they are offered combined.
Inheritance patternAutosomal recessive for both conditions
Gene / MutationBCAN — ~15.7 kb deletion (EF); FAM83H — deletion c.977del p.(Pro326Hisfs*258) (CCS)
PenetranceComplete or nearly complete penetrance in homozygotes for EF and for CCS separately. Heterozygotes asymptomatic.
Codehlip
Turnaround time15 days
Price69,21 €

Incidence

Cavalier King Charles Spaniel. Carrier frequency is not systematically published in the accessible literature (limited data). Breed screening before breeding is recommended.

Breeder management

- Genotype breeding animals for EF (BCAN) and CCS (FAM83H) before mating
- Do not mate two carriers for the same variant
- A carrier may be mated to a clear animal and the offspring intended for breeding must be tested
- After a confirmed clinical case, do not repeat the parental mating and inform the buyer
- CCS is not merely a cosmetic problem: dry eye affects quality of life and must be treated

Specialist notes

EF must be distinguished from myelinopathies, idiopathic epilepsy, myasthenia and congenital myopathies. The episodic hypertonic presentation with preserved consciousness is suggestive. CCS requires ophthalmic assessment (Schirmer test, fluorescein staining) and management of the tear film; in severe forms surgery may be considered. The coexistence of EF+CCS in the same animal homozygous for both is possible and complicates management.

References

1. Forman OP et al. 2012. Parallel mapping and simultaneous sequencing reveals deletions in BCAN and FAM83H associated with discrete inherited disorders in a domestic dog breed. PLoS Genet. PMID: 22253609
2. Gill JL et al. 2012. A canine BCAN microdeletion associated with episodic falling syndrome. Neurobiol Dis. PMID: 21821125
3. Urkasemsin G et al. 2014. Canine paroxysmal movement disorders. Vet Clin North Am Small Anim Pract. PMID: 25441627
4. OMIA:001592-9615 (Episodic falling, BCAN) y OMIA:001683-9615 (queratoconjuntivitis sicca congénita e ictiosis, FAM83H).

Tests included in this pack (2)

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