KELLY

Kelly was tested in 2021 - She was also DNA profiled for ASCA, which confirmed her parents are, in fact, her parents. 

• Normal (Clear) Multifocal retinopathy 1 WT/WT
• Normal (Clear) Coagulation factor VII deficiency WT/WT
• Normal (Clear) Hyperuricosuria WT/WT
• Normal (Clear) Neuronal ceroid lipofuscinosis 6 WT/WT
• Normal (Clear) Degenerative Myelopathy (Common Variant) WT/WT
• Normal (Clear) Progressive retinal atrophy, Progressive rod-cone degeneration WT/WT
• Normal (Clear) Collie eye anomaly WT/WT
• Normal (Clear) Multidrug resistance 1 WT/WT
• Normal (Clear) Exercise-induced collapse WT/WT
• Normal (Clear) Hereditary cataracts (Australian Shepherd type) WT/WT
• Normal (Clear) Cone degeneration WT/WT
• Normal (Clear) Intestinal Cobalamin Malabsorption (Border Collie type) WT/WT
• Normal (Clear) Von Willebrand disease I WT/WT
• Normal (Clear) Neuronal ceroid lipofuscinosis 8 (Australian Shepherd type) WT/WT
• Normal (Clear) Intestinal Cobalamin Malabsorption (Australian Shepherd Type) WT/WT
• Normal (Clear) Craniomandibular Osteopathy WT/WT
• Normal (Clear) - No CDDY or Increased IVDD Risk Chondrodystrophy with Intervertebral Disc Disease Risk Factor (CDDY with IVDD) WT/WT
•  Normal - No Leg Shortening Associated with CDPAChondrodysplasia (CDPA)cd/cd
•  D Locus (Dilute) Non Dilute Does not carry dilute
• S Locus (White Spotting, Parti, or Piebald) No white spotting, parti, or piebald
• T Locus (Natural Bobtail) Normal Tail