Dawson's Royal Companions

Parent health testing

Goldendoodle

Miniature Poodle

• Hip Dysplasia (Preliminary), Hip Dysplasia

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  Hip testing reduces the chance of passing down hip dysplasia, which is primarily found in large breed dogs and can cause hip pain and the eventual loss of the function of the hip joint.

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• Elbow Dysplasia Finals (OFA, BVA, SV, FCI)

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  Elbow testing reduces the chance of passing down elbow dysplasia, which is primarily found in large breed dogs and can cause arthritis in the elbow joint and front leg lameness.

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• Gonioscopy, Eye Examination (rDVM, not registered with OFA)

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  Eye testing reduces the chance of passing down a wide range of hereditary eye illnesses including retinal dysplasia, lens luxation, and glaucoma, which can cause impared vision or blindness.

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• Cardiac Evaluation (rDVM, not registered with OFA)

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  Heart testing reduces the chance of passing down congenital heart disease, which can cause a range of symptoms ranging from trouble exercising to heart failure.

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• Patellar Luxation

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  Knee testing reduces the chance of passing down Patellar Luxation, which results in the kneecap becoming displaced or dislocated and can cause mild to severe joint pain.

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• Ichthyosis, Golden Retriever Type, Shoulder Osteochondrosis

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  A breeder may perform additional tests on their dogs that do not fall into these general categories. These tests may be more uncommon or very specific to a particular breed.

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• Multiple Drug Sensitivity (MDR1), Thrombopathia (RASGRP2 Exon 8), Thrombopathia, Newfoundland Type, Thrombopathia, Finnish Spitz Type, Thrombopathia, Basset Hound Type, Thrombopathia, American Eskimo Dog Type, von Willebrand Disease II (vWD II), von Willebrand Disease III (vWD III), Shetland Sheepdog Type, von Willebrand Disease III (vWD III), Scottish Terrier Type, von Willebrand Disease III (vWD III), Kooikerhondje Type, von Willebrand Disease III (vWD III), Leukocyte Adhesion Deficiency, Type III, Leukocyte Adhesion Deficiency, Type I, Congenital Macrothrombocytopenia, Elliptocytosis, Glanzmann's Thrombasthenia, Otterhound Type, May-Hegglin Anomaly, Prekallikrein Deficiency, Fletcher Trait, Pyruvate Kinase Deficiency (PKD), Terrier Type, Pyruvate Kinase Deficiency (PKD), Pug Type, Pyruvate Kinase Deficiency (PKD), Labrador Retriever Type, Pyruvate Kinase Deficiency (PKD), Labrador Retriever Type, Pyruvate Kinase Deficiency (PKD), Cairn Terrier Type, Glanzmann's Thrombasthenia, Great Pyrenees Type, Pyruvate Kinase Deficiency (PKD), Beagle Type, Pyruvate Kinase Deficiency (PKD), Basenji Type , Pyruvate Kinase Deficiency, Basenji Type (PKD), Ligneous Membranitis, LM (PLG), P2RY12 Receptor Platelet Disorder, Methemoglobinemia, Bernard-Soulier Syndrome, Cocker Spaniel Type, Congenital Hypothyroidism with Goiter, Terrier Type (CHG), Congenital Hypothyroidism with Goiter (CHG), Congenital Dyshormonogenic Hypothyroidism with Goiter, Shih Tzu Type, Compliment 3 Deficiency (C3), Severe Combined Immunodeficiency Disease, X-Linked (XSCID), Corgi Type, Severe Combined Immunodeficiency Disease, X-Linked, Basset Hound Type (XSCID), Severe Combined Immunodeficiency Disease, Terrier Type, Severe Combined Immunodeficiency Disease, Frisian Water Dog Type, PRA (PRA1), Papillon Type, PRA (PRA1), Italian Greyhound Type, PRA, Cone-Rod Dystrophy 1 (PRA-crd1), Cone-Rod Dystrophy 1 (crd1), American Staffordshire Terrier Type, Cone-Rod Dystrophy (crd4), X-Linked Progressive Retinal Atrophy 1, PRA3, Tibetan Terrier and Spaniel Type, Day Blindness, Achromatopsia, PRA Dominant (DPRA), Mastiff Type, Multifocal Retinopathy 1 (CMR1), Coton de Tulear Type, Multifocal Retinopathy 1 (CMR1), Multifocal Retinopathy 2 (CMR2), Multifocal Retinopathy 3 (CMR3), Primary Open Angle Glaucoma, Petit Basset Griffon Vendeen Type, Primary Open Angle Glaucoma, Basset Hound Type, Primary Open Angle Glaucoma and Primary Lens Luxation (POAG/PLL), Shar-Pei Type, Primary Open Angle Glaucoma (ADAMST17 Exon 11), Primary Open Angle Glaucoma (ADAMST10 Exon 9), Primary Open Angle Glaucoma (ADAMST10 Exon 17), Hereditary (Juvenile) Cataracts (HC; JC), Primary Lens Luxation (PLL), Congenital Stationary Night Blindness (CSNB), Macular Corneal Dystrophy, MCD (CHST6), 2,8-Dihydroxyadenine (2,8-DHA) Urolithiasis, Cystinuria Type 1, Newfoundland (PennGen), Cystinuria Type 1A, Newfoundland Type, Cystinuria Type 1A, Labrador Retriever Type, Polycystic Kidney Disease (PKD), Primary Hyperoxaluria, Protein-Losing Nephropathy (PLN; NPHS1 Gene Variant), X-Linked Progressive Retinal Atrophy (XL-PRA), Familial Nephropathy, English Springer Spaniel Type, Familial Nephropathy, Cocker Spaniel Type, Fanconi Syndrome, Primary Ciliary Dyskinesia, Kartagner Syndrome (PCD), Dry Eye Curly Coat Syndrome (CKSID), X-Linked Anhidrotic Ectodermal Dysplasia, Dachshund type, Renal Cystadenocarcinoma and Nodular Dermatofibrosis (RCND), Fucosidosis, Glycogen Storage Disease Type II or Pompe's Disease (GSD II), Glycogen Storage Disease Type IA, GSD IA, Glycogen Storage Disease Type IIIA, GSD IIIA, Glycogen Storage Disease Type VII, Phosphofructokinase Deficiency, PFK Deficiency (PFKM Wachtelhund Variant), Glycogen Storage Disease Type VII, GSD VII, Lagotto Storage Disease (LSD), Neuronal Ceroid Lipofuscinosis 8 (NCL8), Setter Type, Neuronal Ceroid Lipofuscinosis 8 (NCL8), Australian Shepherd Type, Neuronal Ceroid Lipofuscinosis 7 (NCL7), Neuronal Ceroid Lipofuscinosis 6 (NCL 6), Neuronal Ceroid Lipofuscinosis 5 (NCL5), Golden Retriever Type, Neuronal Ceroid Lipofuscinosis 5 (NCL5), Border Collie Type, Neuronal Ceroid Lipofuscinosis 4A (NCL4A), American Staffordshire Terrier Type, Neuronal Ceroid Lipofuscinosis 2 (NCL2), Neuronal Ceroid Lipofuscinosis 1 (NCL1), Dachshund Type, Neuronal Ceroid Lipofuscinosis 1 (NCL1), Cane Corso Type, Neuronal Ceroid Lipofuscinosis 12 (NCL12), Australian Cattle Dog Type, Neuronal Ceroid Lipofuscinosis 10 (NCL10), American Bulldog Type, GM2 Gangliosidosis, Poodle Type, GM1 Gangliosidosis, Portuguese Water Dog Type, GM1 Gangliosidosis (HEXB), Shiba Inu Type, GM1 Gangliosidosis (GLB1), Shiba Inu Type, GM1 Gangliosidosis, Alaskan Husky Type, Gangliosidosis GM2, Japanese Chin Type, Familial Enamel Hypoplasia (FEH), Samoyeds, Familial Enamel Hypoplasia (FEH), Parson Russell Terrier Type, Familial Enamel Hypoplasia (FEH), Italian Greyhound Type, Deafness and Vestibular Syndrome of Dobermans, DVDobs, DINGS, Deafness and Vestibular Dysfunction, Doberman Pinscher Type, Recurrent Inflammatory Pulmonary (Collie Type) - Single Assay Test, Encephalopathy, Alaskan Husky Type, Alexander Disease, Spinocerebellar Ataxia with Myokymia (KCNJ10), Cerebellar Ataxia, Spinone Italiano Type, Cerebellar Ataxia, Finnish Hound Type, Cerebellar Ataxia 2, Belgian Shepherd Type, Late Onset Ataxia, Spinocerebellar Ataxia (LOA, SCA), Spongy Degeneration with Cerebellar Ataxia (SDCA1) mutation originally found in Belgian Shepherd Dog and Malinois, Benign Familial Juvenile Epilepsy (BFJE), Fetal-Onset Neonatal Neuroaxonal Dystrophy (MFN1), X-Linked Tremors, Shaking Puppy Syndrome (SPS), Neuroaxonal Dystrophy (NAD), Spanish Water Dog Type, Neuroaxonal Dystrophy (NAD), Rottweiler Type, L-2-Hydroxyglutaric Aciduria (L2HGA), Staffordshire Bull Terrier Type, Polyneuropathy (NDRG1), Alaskan Malamute Type, Narcolepsy, Doberman Pinscher Type, Narcolepsy, Labrador Retriever Type, Narcolepsy, Dachshund Type, Canine Multiple System Degeneration, Kerry Blue Terrier Type, Canine Multiple System Degeneration (Chinese Crested Type), Laryngeal Paralysis (Bull Terrier Type) - Single Assay Test, Acral Mutilation Syndrome (AMS), Sensory Neuropathy, Border Collie Type (SN), Polyneuropathy 1, Leonberger and Saint Bernard Type, Juvenile Myoclonic Epilepsy (JME), Polyneuropathy 2, Leonberger and Saint Bernard Type, Spongy Degeneration with Cerebellar Ataxia (SDCA2) mutation originally found in Belgian Shepherd Dog, Dilated Cardiomyopathy 2 (DCM2), Dilated Cardiomyopathy 1 (DCM1), Long QT Syndrome, Cardiomyopathy and Juvenile Mortality (YARS2), Duchenne Muscular Dystrophy, Golden Retriever Type, Cavalier King Charles Spaniel Muscular Dystrophy (CKCS-MD), Limb Girdle Muscular Dystrophy, Boston Terrier, Ullrich Congenital Muscular Dystrophy, Centronuclear Myopathy (CNM), Exercise Induced Collapse (EIC), Centronuclear Myopathy (CNM), Great Dane Type, Muscular Hypertrophy/Myostatin Deficiency, Bully Whippet Syndrome (Double Muscling), Myotonia Congenita, Schnauzer Type, Myotonia Congenita, Australian Cattle Dog Type, Myotubular Myopathy, Labrador Retriever Type, Inflammatory Myopathy (Myositis), Pyruvate Dehydrogenase Phosphatase 1 Deficiency (PDP1), Malignant Hyperthermia (MH), Intestinal Cobalamin Malabsorption (IGS CUBN Exon 8), Border Collie Type, Intestinal Cobalamin Malabsorption (IGS CUBN Exon 53), Border Collie Type, Lundehund Syndrome, Congenital Myasthenic Syndrome (CMS), Spanish Water Dog Type, Congenital Myasthenic Syndrome (CMS), Old Danish Pointer Type, Congenital Myasthenic Syndrome (CMS), Labrador Retriever Type, Congenital Myasthenic Syndrome (CMS), Jack Russell Terrier Type, Episodic Falling Syndrome (EFS), Adult Paroxysmal Dyskinesia, Juvenile Laryngeal Paralysis & Polyneuropathy (JLPP), Dystrophic Epidermolysis Bullosa, Ichthyosis, Great Dane Type, Ichthyosis, Golden Retriever Type 2, Focal Non-Epidermolytic Palmoplantar Keratoderma, Pachyonychia Congenita (KRT16), Hereditary Footpad Hyperkeratosis (FAM83G), Hereditary Footpad Hyperkeratosis (DSG1), Hereditary Nasal Parakeratosis (HNPK), Musladin-Leuke Syndrome (MLS), Canine Multifocal Retinopathy (cmr3; BEST1 Exon 10 SNP), Bald Thigh Syndrome (IGFBP5), Lethal Acrodermatitis (LAD), Bull Terrier Type, Ehlers-Danlos Syndrome, Cleft Palate (DLX6), Cleft Palate (ADAMTS20), Hereditary Vitamin D-Resistant Rickets (HVDRR), Retinal Dysplasia/Oculoskeletal Dysplasia 1 (RD OSD), Osteogenesis Imperfecta (OI), Dachshund Type, Osteogenesis Imperfecta (OI), Beagle Type, Skeletal Dysplasia (SD2), Retinal Dysplasia/Oculoskeletal Dysplasia 2, Craniomandibular Osteopathy (CMO), Chondrodysplasia/Dwarfism, Chondrodystrophy and IVDD Risk (CDDY-IVDD), Mucopolysaccharidosis Type IIIB (MPS IIIB), Full Embark Panel, Chondrodystrophy (CDDY and IVDD Risk) with or without Chondrodysplasia (CDPA), DNA Disease Panel, Ichthyosis, Golden Retriever Type 1, Degenerative Myelopathy (DM; SOD1A), PRA, Rod-Cone Degeneration (PRA-prcd), Neonatal Encephalopathy with Seizures (NEwS), von Willebrand Disease I (vWD I), PRA, Golden Retriever 2, PRA, Golden Retriever 1

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  Genetic testing reduces the chance of passing down a wide variety of hereditary diseases of differing prevalence and severity such as Progressive Retinal Atrophy (an eye disease) and Von Willebrand's Disease (a blood disease).

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