Lucy’s legacy dachshunds

Parent health testing

• Hip Dysplasia (rDVM, not registered)

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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 (Preliminary), Elbow Dysplasia Finals (OFA, BVA, SV, FCI), Elbow Dysplasia (rDVM, not registered)

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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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• 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 (registered with OFA), 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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• Dermoid Sinus (DS), Dentition, Cystinuria Urine Test (PennGen), Congenital Deafness (BAER, registered with OFA), Brucellosis, Canine Good Citizen (CGC)

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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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• ESSFTA/University of Missouri DNA Bank, Epidermolysis Bullosa (Eurasier), Epidermolytic Hyperkeratosis, Encephalopathy, Alaskan Husky Type, Elliptocytosis, Ehlers-Danlos Syndrome, Ectodermal Dysplasia, X-Linked (Shepherd Type), Ectodermal Dysplasia, X-Linked (Dachshund Type), Ectodermal Dysplasia, Chesapeake Bay Retriever Type, Early Retinal Degeneration, Early Onset Progressive Retinal Atrophy (EOPRA), Early Adult Onset Deafness (EAOD), Dystrophic Epidermolysis Bullosa, Duchenne Muscular Dystrophy, Pembroke Welsh Corgi Type, Duchenne Muscular Dystrophy, Norfolk Terrier Type, Duchenne Muscular Dystrophy, Golden Retriever Type, Dry Eye Curly Coat Syndrome (CKSID), Dominant Black DNA Test, DNA Repository, DNA Profile, DNA Coat/Trait Panel, D Locus (Dilute) DNA test, Dilated Cardiomyopathy (Schnauzer Type), Dilated Cardiomyopathy 2 (DCM2), Dilated Cardiomyopathy 1 (DCM1), Diffuse cystic renal dysplasia and hepatic fibrosis, Dermoid sinus, Dermatomyositis, Dental Hypomineralization (DH), Degenerative Myelopathy Early-Onset Risk Modifier, Pembroke Welsh Corgi Type, Degenerative Myelopathy (DM; SOD1B), Bernese Mountain Dog Type, Degenerative Myelopathy (DM; SOD1A), Deafness and Vestibular Syndrome of Dobermans, DVDobs, DINGS, Deafness and Vestibular Dysfunction, Doberman Pinscher Type, Day Blindness, Achromatopsia, Dandy-Walker-like Malformation (DWLM), Toy Fox Terrier Type, Dandy-Walker-like Malformation (DWLM), Eurasier Type, Cystinuria Type II-B, Miniature Pinscher Type, Cystinuria Type II-A, Australian Cattle Dog Type, Cystinuria Type 3 (Variant 3), Bulldog Type Risk Factor, Cystinuria Type 3 (Variant 1 & 2), Bulldog Type Risk Factor, Cystinuria Type 3, French Bulldog Type Risk Factor, Cystinuria Type 3, English Mastiff Type Risk Factor, Cystinuria Type 1, Newfoundland (PennGen), Cystinuria Type 1A, Newfoundland Type, Cystinuria Type 1A, Labrador Retriever Type, Cystic Renal Dysplasia and Hepatic Fibrosis, Cyclic Neutropenia, Grey Collie Syndrome (CN), Craniomandibular Osteopathy (CMO), Copper Toxicosis, Labrador Retriever Type, Copper Toxicosis, Labrador Retriever ATP7A, Copper Toxicosis, Bedlington Terrier Type (COMMD1), Congenital Stationary Night Blindness (CSNB), 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, Congenital Methemoglobinemia, Pomeranian Type, Congenital Macrothrombocytopenia, Congenital Hypothyroidism with Goiter, Terrier Type (CHG), Congenital Hypothyroidism with Goiter (CHG), Congenital Eye Disease; mutation originally found in Irish Soft Coated Wheaten Terrier, Congenital Dyshormonogenic Hypothyroidism with Goiter, Shih Tzu Type, X-Linked Tremors, Shaking Puppy Syndrome (SPS), Cone-Rod Dystrophy (crd4), Cone-Rod Dystrophy 2 (crd2), American Pitbull Terrier Type, Cone-Rod Dystrophy 1 (crd1), American Staffordshire Terrier Type, Cone Degeneration, Labrador Retriever Type, Cone Degeneration, Husky Type, Cone Degeneration, German Shorthaired Pointer Type, Cone Degeneration, German Shepherd Dog Type, Cone Degeneration, Compliment 3 Deficiency (C3), Collie Eye Anomaly (CEA), Cleft Palate (ADAMTS20), Cleft Palate (DLX6), Chondrodystrophy, Norwegian Elkhound and Karelian Bear Dog Variant (ITGA10), Chondrodystrophy (CDDY and IVDD Risk) with or without Chondrodysplasia (CDPA), Chondrodystrophy and IVDD Risk (CDDY-IVDD), Chondrodysplasia/Dwarfism, Cerebral Dysfunction, Frisian Stabyhoun Type, Cerebellar Degeneration, Cerebellar Cortical Degeneration (CCD), Cerebellar Ataxia, Spinone Italiano Type, Cerebellar Ataxia, Finnish Hound Type, Cerebellar Ataxia 2, Belgian Shepherd Type, Centronuclear Myopathy (CNM), Great Dane Type, Centronuclear Myopathy (CNM), Cavalier King Charles Spaniel Muscular Dystrophy (CKCS-MD), Catalase Deficiency, Cardiomyopathy and Juvenile Mortality (YARS2), Canine Scott Syndrome (CSS), Canine Multiple System Degeneration, Kerry Blue Terrier Type, Canine Multiple System Degeneration (Chinese Crested Type), Canine Multifocal Retinopathy (cmr3; BEST1 Exon 10 SNP), Brachycephaly, Bernard-Soulier Syndrome, Cocker Spaniel Type, Benign Familial Juvenile Epilepsy (BFJE), Behavior Propensity, Belgian Malinois, Bald Thigh Syndrome (IGFBP5), Ataxia, Norwegian Buhund Type, Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC), Animal Genetics Panel, Amelogenesis Imperfecta (AI), Italian Greyhound Type, Amelogenesis Imperfecta (AI), Akita Type, Alexander Disease, Alanine Aminotransferase Activity, Agouti DNA Test, Adult Paroxysmal Dyskinesia, Adult Onset Neuropathy (AON), Acute Respiratory Distress Syndrome, Dalmatian Type, Acral Mutilation Syndrome (AMS), 2,8-Dihydroxyadenine (2,8-DHA) Urolithiasis, DNA Disease Panel

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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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