Dream Hounds of Michigan

Parent health testing

• Osteogenesis Imperfecta (OI), Dachshund Type, Osteogenesis Imperfecta (OI), Beagle Type, Osteochondrodysplasia, Miniature Poodle Type, Skeletal Dysplasia (SD2), Craniomandibular Osteopathy (CMO), Chondrodystrophy (CDDY and IVDD Risk) with or without Chondrodysplasia (CDPA), Mucopolysaccharidosis Type IIIB (MPS IIIB), Epidermolysis Bullosa (Eurasier), Mucopolysaccharidosis Type VI (MPS VI), Pituitary Dwarfism (LHX3), Progressive Retinal Atrophy (PRA), Generalized, Hereditary Vitamin D-Resistant Rickets (HVDRR), Cleft Palate (ADAMTS20), Oculocutaneous Albinism (Small Breed Type), Musladin-Leuke Syndrome (MLS), Hereditary Footpad Hyperkeratosis (DSG1), Ichthyosis (KRY10), Laryngeal Paralysis (Bull Terrier Type) - Single Assay Test, Adult Paroxysmal Dyskinesia, 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, Lundehund Syndrome, Intestinal Cobalamin Malabsorption (IGS CUBN Exon 8), Border Collie Type, Malignant Hyperthermia (MH), Pyruvate Dehydrogenase Phosphatase 1 Deficiency (PDP1), Hypocatalasia, X-Linked Myotubular Myopathy, Centronuclear Myopathy (CNM), Ullrich Congenital Muscular Dystrophy, Long QT Syndrome, Dilated Cardiomyopathy (Schnauzer Type), Dilated Cardiomyopathy 2 (DCM2), Dilated Cardiomyopathy 1 (DCM1), Spongy Degeneration with Cerebellar Ataxia (SDCA1) mutation originally found in Belgian Shepherd Dog and Malinois, Juvenile Myoclonic Epilepsy (JME), Polyneuropathy 1, Leonberger and Saint Bernard Type, Sensory Neuropathy, Border Collie Type (SN), Acral Mutilation Syndrome (AMS), Juvenile Laryngeal Paralysis & Polyneuropathy (JLPP), Canine Multiple System Degeneration (Chinese Crested Type), Canine Multiple System Degeneration, Kerry Blue Terrier Type, L-2-Hydroxyglutaric Aciduria (L2HGA), Staffordshire Bull Terrier Type, Neuroaxonal Dystrophy (NAD), Spanish Water Dog Type, X-Linked Tremors, Shaking Puppy Syndrome (SPS), Hypomyelination, Weimaraner Type, Fetal-Onset Neonatal Neuroaxonal Dystrophy (MFN1), Degenerative Myelopathy (DM; SOD1A), Benign Familial Juvenile Epilepsy (BFJE), Hereditary Ataxia, Cerebellar Ataxia, Spinocerebellar Ataxia with Myokymia (KCNJ10), Neonatal Cortical Cerebellar Degeneration (NCCD), Recurrent Inflammatory Pulmonary (Collie Type) - Single Assay Test, Deafness and Vestibular Dysfunction, Doberman Pinscher Type, Persistent Müllerian Duct Syndrome, Familial Enamel Hypoplasia (FEH), Italian Greyhound Type, Globoid Cell Leukodystrophy (GCL), Terrier Type, Gangliosidosis GM2, Japanese Chin Type, GM2 Gangliosidosis, Poodle Type, GM1 Gangliosidosis, Portuguese Water Dog Type, GM1 Gangliosidosis, Alaskan Husky Type, GM1 Gangliosidosis (GLB1), Shiba Inu Type, Neuronal Ceroid Lipofuscinosis 10 (NCL10), American Bulldog 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), Border Collie Type, Neuronal Ceroid Lipofuscinosis 4A (NCL4A), American Staffordshire Terrier Type, Neuronal Ceroid Lipofuscinosis 2 (NCL2), Neuronal Ceroid Lipofuscinosis 1 (NCL1), Dachshund Type, Lagotto Storage Disease (LSD), Glycogen Storage Disease Type VII, Phosphofructokinase Deficiency, PFK Deficiency (PFKM Wachtelhund Variant), Mucopolysaccharidosis VII (MPS VII GUSB), Shepherd Type, Mucopolysaccharidosis VII (MPS VII), Brazilian Terrier Type, Mucopolysaccharidosis IIIA (MPS IIIA), Dachshund Type, Glycogen Storage Disease Type IIIA, GSD IIIA, Glycogen Storage Disease Type IA, GSD IA, Fucosidosis, Renal Cystadenocarcinoma and Nodular Dermatofibrosis (RCND), Dry Eye Curly Coat Syndrome (CKSID), Primary Ciliary Dyskenesia (Malamute Type) - Single Assay Test, Fanconi Syndrome, Familial Nephropathy, English Springer Spaniel Type, Familial Nephropathy, Cocker Spaniel Type, Protein-Losing Nephropathy (PLN; NPHS1 Gene Variant), Primary Hyperoxaluria, Polycystic Kidney Disease (PKD), Cystinuria Type II-B, Miniature Pinscher Type, Cystinuria Type II-A, Australian Cattle Dog Type, Cystinuria Type 1A, Labrador Retriever Type, Congenital Stationary Night Blindness (CSNB), Primary Lens Luxation (PLL), Primary Open Angle Glaucoma and Primary Lens Luxation (POAG/PLL), Shar-Pei Type, Primary Open Angle Glaucoma, Basset Hound Type, Primary Open Angle Glaucoma (ADAMST17 Exon 11), Primary Open Angle Glaucoma (ADAMST10 Exon 9), Canine Multifocal Retinopathy (cmr3; BEST1 Exon 10 SNP), X-Linked Progressive Retinal Atrophy 1, Severe Combined Immunodeficiency Disease, X-Linked (XSCID), Corgi Type, Severe Combined Immunodeficiency Disease, Terrier Type, Compliment 3 Deficiency (C3), Congenital Hypothyroidism with Goiter, Terrier Type (CHG), Methemoglobinemia, Ligneous Membranitis, LM (PLG), Trapped Neutrophil Syndrome, Cohen Syndrome (TNS), Pyruvate Kinase Deficiency (PKD), Terrier Type, Pyruvate Kinase Deficiency (PKD), Pug Type, Pyruvate Kinase Deficiency (PKD), Labrador Retriever Type, Pyruvate Kinase Deficiency (PKD), Beagle Type, Pyruvate Kinase Deficiency, Basenji Type (PKD), Prekallikrein Deficiency, Fletcher Trait, May-Hegglin Anomaly, Glanzmann's Thrombasthenia, Otterhound Type, Glanzmann's Thrombasthenia, Great Pyrenees Type, Congenital Macrothrombocytopenia, von Willebrand Disease III (vWD III), Thrombopathia, American Eskimo Dog Type, Thrombopathia (RASGRP2 Exon 8), Thrombopathia, Basset Hound Type, Factor VII Deficiency, P2RY12 Receptor Platelet Disorder

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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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