Combination Lapphund

General description

includes (15 Euro patent fee): Canine multi-focal retinopathy (CMR3), Degenerative myelopathy (DM exon 2), Glycogen storage disease (GSDII) (Pompe disease), progressive retinal atrophy (prcd-PRA)*

Breeds

Finnish Lapponian Dog, Lapponian Herder, Swedish Lapphund

Order details
Test number8249
Sample material0.5 ml EDTA blood, 2x cheek swab, 1x special swab (eNAT)
Test duration7-14 working days

Degenerative myelopathy exon 2 (DM exon 2)

Test specifications
Symptom complexneuromuscular
Inheritanceautosomal recessive with age-dependent incomplete penetrance; a risk factor associated with DM is detected.
Age of onsetab 8 years
CausalityHigh-risk factor
GeneSOD1
MutationG-A
LiteratureOMIA:000263-9615

Glycogen storage disease (GSD II) (Pompe disease)

Test specifications
Symptom complexsystemic
Inheritanceautosomal recessive
Age of onsetfrom birth
Causalitycausally
GeneGAA
MutationC-T
LiteratureOMIA:000419-9615

Progressive retinal atrophy (prcd-PRA)

Test specifications
Symptom complexophthalmic
Inheritanceautosomal recessive
Causalitycausally
GenePRCD
MutationC-T
LiteratureOMIA:001298-9615