this test enables you to identify if a dog is docked or has a natural short tail. Jack Russell Terrier , , Symptoms continue to progress and by 4.5 years of age, significant sight loss is reported. , German Spitz , instructions on this link, Progressive Retinal Atrophy (Dominant PRA), Globoid Cell Leukodystrophy (Krabbe Disease), CSNB (Congenital Stationary Night Blindness), CLAD (Canine Leukocyte Adhesion Deficiency), PK Deficiency (Pyruvate Kinase Deficiency), PFK Deficiency (Phosphofructokinase deficiency), X-Linked Severe Combined Immunodeficiency (X-SCID), Hereditary Myopathy / Centronuclear Myopathy (HMLR, CNM), Canine Cyclic Neutropenia (Gray Collie Syndrome), Progressive Retinal Atrophy (cord1- PRA / crd4 PRA), L-2-HGA ( L- 2 - hydroxyglutaric aciduria ) L2HGA, von Willebrand disease Type III (vWD III), Neuronal Ceroid Lipofuscinosis ( CL / NCL ), PDP 1 Deficiency (Pyruvate Dehydrogenase Phosphatase 1 Deficiency), Juvenile Brain Disease ( JBD ) / Juvenile Encephalopathy ( Epilepsy ), French Bulldog DNA bundle (DM + HSF4 + CHG + Cy + CMR + CDDY/CDPA), Leonberger DNA bundle (LPN1+LPN2+LEMP+LPPN3), BRAF Mutation ( transitional cell carcinoma ), MDR1 Gene Varian / Ivermectin Sensitivity *, Dwarfism (Pituitary Dwarfism / Hypopituitarism), Degenerative Myelopathy / Degenerative Radiculomyelopathy) DM (Exon 2), Greyhound Neuropathy (Hereditary Neuropathy), Brittle Bone Disease (Osteogenesis Imperfecta), Familial Nephropathy (FN) / Hereditary Nephropathy *, Familial Nephropathy (FN) / Hereditary Nephropathy, Myostatin Mutation ("Bully" Whippet)/ Double Muscling, Hereditary Nephritis / Samoyed Hereditary Glomerulopathy, Episodic Falling in Cavalier King Charles Spaniel (EF), CKCS Pack A: Episodic Falling + Dry Eye Curly Coat syndrome, Congenital Hypothyreosis / hypothyroidism ( CHG ), Neonatal Cortical Cerebellar Abiotrophy (NCCD), Progressive Retinal Atrophy (generalized PRA), Progressive retinal atrophy ( rcd4-PRA) / LOPRA, Alaskan Malamute Polyneuropathy (AMPN / IPAM / HPAM), Pug Dog Encephalitis (PDE) / Necrotizing Meningoencephalitis (NME), Pompe's Disease (Glycogen Storage Disease type II / GSDII), Cobalamin Malabsorption (Imerslund-Grsbeck syndrome (IGS)), CMSD (Canine Multiple System Degeneration), Lagotto DNA bundle: JE+NAD+Furnishing+LSD+prcd-PRA+SLC, Progressive Retinal Atrophy (prcd-PRA): (8094P / 8127), Digital Hyperkeratosis (DH) (Hereditary Footpad Hyperkeratosis / Corny Feet), Degenerative Myelopathy / degenerative radiculomyelopathy) DM (Exon 1), Degenerative Myelopathy / degenerative radiculomyelopathy) DM (Exon 1 + Exon 2), Ectodermal Dysplasia / Skin Fragility Syndrome (ED / SFS), Hypomyelination (Shaking Puppy Syndrome) SPS, JRT and PRT Pack B: LOA + SCA + PLL + JBD + DM2, Finnish Hound Ataxia / Cerebellar Ataxia (FHA / CAFH), Persistent Mllerian duct syndrome (PMDS), Juvenile Laryngeal Paralysis & Polyneuropathy (JLPP), Postoperative Hemorrhage (P2Y12 / P2RY12), Glanzmann Thrombasthenia (Thrombasthenia, Thrombasthenic thrombopathia, GT), Prekallikrein Deficiency (KTK) / Fletcher Factor Deficiency, C3 Deficiency (Complement Component 3 deficiency), GM2 Gangliosidosis Variant 0 (Sandhoff Disease), Renal Cystadenocarcinoma and Nodular Dermatofibrosis (RCND), Amelogenesis Imperfecta (AI) / Familial Enamel Hypoplasia (FEH), Collie Eye Anomaly (CEA) / Choroidal Hypoplasia (CH) *, Mucopolysaccharidosis type IIIa (MPS IIIA), Progressive Retinal Atrophy (rcd2-PRA) by Laboklin, Ichthyosis ( Epidermolytic Hyperkeratosis (EHK) ), Dwarfism ( Chondrodysplasia / disproportinate short-limbed ), Ichthyosis (Congenital Ichthyosis / Great Dane Ichthyosis), Hemorrhagic Diathesis / Bleeding Diathesis (Canine Scott Syndrom), Glycogen storage disease type Ia (GSD Ia) / VON Grieke Disease, Hyperuricosuria / Urate Stones (HUU, SLC), Leukocyte Adhesion Deficiency type III (LAD III), Canine Multi-Focal Retinopathy (CMR 1/2/3), Retinal Dysplasia (RD) / Oculo Skeletal Dysplasia (OSD)*, Special Offer Chinese Crested: PLL + prcd PRA + rcd3 PRA + DM Exon 2 + CMSD + NCL, Raine Syndrome ( Dental hypomineralization ), Spinal Dysraphism / Neural Tube Defects ( NTD ), Spongy Degeneration with Cerebellar Ataxia ( SDCA1 ), Beagle DNA Bundle : IGS + Factor VII + MLS + NCCD + Osteogenesis imperfecta + PK + POAG + CAT, Poodle DNA Bundle: DM exon2 + rcd4 PRA + NE + prcd-PRA + vWD1, Golden Retriever DNA bundle: GR-PRA1 + GR-PRA2 + Ichthyosis + prcd-PRA + Muscular Dystrophy + NCL, Pug Special Offer: DM Exon2 + MH + PDE / NME + PK + PLL, Aussie DNA bundle: CEA * + DM exon2 + HSF4 + MDR1 + Brachyury + NCL + prcd-PRA *+SLC, Collie DNA Bundle: CEA + DM exon2 + IPD + MDR1 + rcd2-PRA + DMS, Border Collie DNA Bundle: CEA + IGS + MDR1 + Raine + SN + NCL + TNS + GGD, Pack A: CNM + DM exon2 + EIC + HNPK + OSD + prcd-PRA + SD2, Pack B: AxD+Cystinuria+Narcolepsy+Obesity+PK+SLC+STGD+XL-MTM, Catalase Deficiency ( CAT ) / Hypocatalasemia / Acatalasia, Spongy Degeneration with Cerebellar Ataxia ( SDCA2 ), Belgian Shepherd Special Offer : SDCA1 + SDCA2+ CJM + CACA, Acute Respiratory Distress Syndrome ( ARDS ), POAG / PLL Primary Open Angle Glaucoma (POAG) and Primary Lens Luxation (PLL), Shar Pei auto-inflammatory disease (SPAID), Doberman DNA bundle (DM2 + vWDI + Narcolepsy + B Locus + D Locus), Landseer DNA bundle (Cystinuria + DM2 + D-Locus (D1) + MD + Thrombopathia), Rhodesian Ridgeback DNA Bundle (DM2 + Haemophilia A and B + B Locus + JME + D Locus), Rottweiler DNA bundle ( DM2 , LEMP , JLPP , NAD, CL1 , XL - MTM ), Subacute Necrotizing Encephalopathy (SNE), ISDS Exclusive Border Collie DNA Bundle: CEA 1* + IGS + SN + TNS, Lafora Disease (LAF / LD) / Myoclonic Epilepsy, Shetland DNA Bundle: CEA + DM Exon 2 + vWD Type III + MDR1 + CNGA1-PRA, CKCS Pack B: DM Exon2 + Episodic Falling + DryEye + MD + MTC, Old English Sheepdog (Bobtail) DNA bundle: DM Exon2 + EIC + HA + MDR1 + PCD, German Shepherd and Wolfdog DNA Bundle (DM2+PD+HUU+MDR1+ CL1), Neuronal Ceroid Lipofuscinosis Combi in ACD & AUSSIE ( NCL Combi ), Chondrodystrophy (CDDY with IVDD Risk) and Chondrodysplasia (CDPA), Mycobacterium Avium Complex ( MAC ) sensitivity, Australian Cattle Dog bundle (DM Exon2 + NCL + PLL + prcd-PRA (partnerlab) + rcd4-PRA), Dachshund DNA bundle (Osteogenesis imperfecta + NCL + cord1-PRA + crd-PRA), Welsh Corgi DNA bundle (Brachyuria + IVDD-risk + DM exon2 + rcd3-PRA + vWD1), Cocker Spaniel DNA bundle (AMS + FN + prcd PRA), Leukoencephalopathy ( LEP ) / Leukodystrophy ( LD ), Mucopolysaccharidosis type IIIb ( MPS3b ), Renal dysplasia and hepatic fibrosis ( RDHN ), NECAP-1 Progressive Retinal Atrophy ( NECAP1 PRA / NECAP PRA5), Retinal dysplasia ( RD ) / Oculoskeletal Dysplasia ( OSD 3 ), Shiba Inu DNA bundle (GM1 , GM2 , A Locus and E Locus), Copper storage disease - Copper toxicosis (CT) *, Portuguese Waterdog DNA Bundle ( GM1 + prcd PRA + eo-PRA + Improper Coat), Bull Terrier DNA bundle ( LAD + PLL + LP + PKD ), Australian Shepherd KC DNA bundle (MDR1+ prcd-PRA + CEA + HSF4), Beagle KC DNA bundle (F7 + IGS BG + MLS + NCCD), Border Collie KC DNA bundle (GG +IGS BC+NCL BC+TNS+SN+MDR1+CEA), English Springer Spaniel (ESS) KC DNA bundle (AMS+cord1-PRA+Fucosidosis+PFKD), French Bulldog KC DNA bundle (DM Exon2+SLC+HSF4), German Shepherd KC DNA bundle (DM Exon2+F8+MDR1), Golden Retriever KC DNA bundle (GR1-PRA+GR2-PRA+Ichthyosis), Labrador Retriever KC DNA bundle (EIC+HNPK+SD2+CNM+MCD+STGD+prcd-PRA), Cardiomyopathy with Juvenile Mortality (CJM), Progressive Retinal Atrophy Type B1 PRA (HIVEP3), Dwarfism ( Disproportionate Dwarfism ) DD, SCWT GB-Club bundle (DM Exon2 + PLN + RBP4), Succinic semialdehyde dehydrogenase deficiency (SSADHD), Progressive Retinal Atrophy Early Onset (EO-PRA), Laryngeal Paralysis - Polyneuropathy ( LPPN3 ), Papillon DNA bundle (pap-PRA + vWD1 + NAD + DM + F7), Great Swiss Mountain Dog DNA bundle (SLC, P2Y12, MH, DM), Tibetan Terrier DNA bundle (NCL - TT + PLL + rcd4-PRA + PRA3 + DM + PD), Irish (Red and White) Setter DNA bundle (CLAD + Krabbe + vWD1 + rcd1-PRA + rcd4-PRA), Miniature Schnauzer Bundle (CMT, MAC, Myotonia congenita, PMDS, TypB1-PRA, Comma-defect), American Cocker Spaniel DNA bundle (prcd-PRA + PFKD + GBM), Cockapoo DNA bundle (AMS+DM+NEWS+vWD1+FN+prcd-PRA+rcd4-PRA), Labradoodle DNA bundle (DM+EIC+HNPK+SD2+NEWS+vWD1+CNM+prcd-PRA+rcd4-PRA), Goldendoodle DNA bundle (DM+NEWS+vWD1+NCL+GR-PRA1+GR-PRA2+prcd-PRA+rcd4-PRA+MD+ICH), Finnish Lapphund DNA bundle (DM + prcd-PRA + GSDII (Pompe) + CMR), Paroxysmal Exercise-Induced Dyskinesia (PED), Giant Schnauzer Club UK bundle ( DM2 + DCM + SLC + PRA5 + prcd-PRA ), Exfoliative Cutaneous Lupus Rrythematosus ( ECLE ) / Lupoid Dermatosis, Bulldog DNA bundle (CMR1 + Cystinuria + DM2 + HUU/SLC), CNS Atrophy with Cerebellar Ataxia (CACA), Copper Toxicosis COMMD1 (Copper Storage Disease ), Macular Corneal Dystrophy ( MCD / CHST6 ), English Springer Spaniel DNA bundle (AMS + FN + SPS + Fucosidosis + PFKD + cord1-PRA ), SCWT DNA bundle (DM + PLN + PxD + RBP4 + SLC ), Colour dilution and neurological defects ( CDN ), Dilated cardiomyopathy DCM1 ( PDK4 ) in Doberman, Dilated cardiomyopathy DCM2 ( Titin ) in Doberman, Dilated cardiomyopathy bundle DCM1 + DCM2 in Doberman, Dilated cardiomyopathy ( DCM ) in Welsh Springer Spaniel, Progressive retinal atrophy ( PRA3 ) in Tibetan Terrier & Tibetan Spaniel, Spongiform leukoencephalomyelopathy (SLEM) *, Chihuahua DNA bundle (CDDY/CDPA (IVDD risk) + MTC + NCL + prcd-PRA), Kromfohrlnder / Kromfohrlander DNA bundle (DM2+DH/HFH+Furnishing+HUU+MDR1+vWD1), Russian Black Terrier DNA bundle (DM2+HUU/SLC+JLPP), Yorkshire Terrier DNA bundle (CDDY/CDPA(IVDD risk)+L2HGA+PLL+prcd_PRA+SNE), Progressive Retinal Atrophy (JPH2 - PRA )in Shih Tzu, Afibrinogenemia (AFG) - a Fibinogen Bleeding Disorder in Dachshund, Spinocerebellar ataxia (Cerebellar ataxia / CA) *, Progressive Retinal Atrophy ( BBS2 type ), Hereditary Xanthinuria Type II (XDH-MOCOS), Coton de Tulear DNA bundle (vWD1 + CDPA/CDDY + CMR + PH), Cavapoo DNA bundle (DM exon2 + EF + DryEye + MD + rcd4 PRA + NE + prcd-PRA + MTC + vWD1), Cerebellar Degeneration and Myositis Complex (CDMC) / Inflammatory Myopathy, Congenital Idiopathic Megaesophagus (CIM), Glen of Imaal Terrier DNA bundle (CRD3 + DM2 + B-Locus ), Scottish Terrier DNA bundle (CDDY/CDPA + CMO + vWD Type 3), German Shorthaired Pointer (GSP) DNA bundle (AMS + ECLE + JEB + VWD2), Barbet DNA bundle (prcd-PRA + vWD 1 + D-Locus + K-Locus), Chesapeake Bay Retriever DNA bundle (DM2 + prcd-PRA + EIC), Cairn Terrier DNA bundle (CMO + Krabbe Disease + MTC + PK), Mitochondrial Fission Encephalopathy (MFE) / Familial Cerebellar Ataxia, this test: Progressive Retinal Atrophy Early Onset (EO-PRA), and, If you have any queries, please contact us on Brittany ( Brittany Spaniel ) Shetland Sheepdog (Sheltie) Neuroaxonal Dystrophy in Spanish Water Dogs is an uncharacterized juvenile-onset genetic disorder that affect Spanish Water Dogs. Additionally, affected dogs displayed varying degrees of compulsory pacing, proprioceptive deficits, decreased menace, visual deficits, positional nystagmus and decreased muscle tone. Kingston NS Airedale Terrier These two new forms are characterised by vision problems starting as early as 1.5 years of age. Australian Cattle Dog The form of progressive rod-cone degeneration (prcd-PRA) is a photoreceptor degeneration in dogs with varying ages of onset. A lot of symptoms relate to Hypothyreosis including general symptoms like lethargy or increase in weight, as well as problems concerning heart, skin and nerves. , Labradoodle Rough Collie , Australian Silky Terrier Progression of the disease is generally slow but highly variable. So there are three conditions a dog can be: it can be clear (genotype N/N or homozygous normal) meaning that it does not carry the mutation and will not develop the prcd-form of PRA. , , Prcd-PRA is inherited as an autosomal recessive trait. These cause a staggering effect that may appear to be arthritis. Spanish Water Dog , , , Karelian Bear Dog Complete the order form and send it together Austrian Pinscher , Labrador Retriever Gina & Scott Peckford , Secondly, degeneration of the cone cells results in complete blindness of the dog, even in full light situations during the day. Labrador Retriever , Affected dogs have a very short lifespan and normally die as puppies. E-Mail: spanishwaterdog@outlook.com. Canaan Dog Norwegian Elkhound Welsh Corgi Boxer , Please note that the Short tail phenotype includes either a complete lack of vertebrae or a short tail with variable length. Pyrenean Mountain Dog (Great Pyrenees) , Miniature American Shepherd Dwarf poodle , , Homozygous for the mutation (T/T): does not exist and thought to be lethal. Lagotto Romagnolo . 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spanish water dog breeders nova scotia