Bedford's All That Magic *Optimal Selection™ CLEAR

DNA Health Testing

DNA & Optimal Selection™ Panel - CLEAR

*HIGHLIGHTS*

Blood Disorders

  • Canine Scott Syndrome (CSS)
  • Hemophilia A (Factor VIII Deficiency)
  • Hemophilia B (Factor IX Deficiency)
  • Phosphofructokinase Deficiency (PFK)
  • Prekallikrein Deficiency
  • Pyruvate kinase deficiency (PKD)
  • Von Willebrand's Disease (vWD), type 1, type 2, type 3

Ocular Disorders

  • Juvenile Hereditary Cataracts (JHC - HSF4)
  • Primary Hereditary Cataract, (PHC)
  • Canine Multifocal Retinopathy 1 (CMR1), Canine Multifocal Retinopathy 2 (CMR2), Canine Multifocal Retinopathy 3 (CMR3)
  • Cone Degeneration, (CD)
  • Cone-Rod Dystrophy (CRD), Cone-Rod Dystrophy 1 (CRD1), Cone-Rod Dystrophy 2 (CRD2)
  • Dominant Progressive Retinal Atrophy (DPRA)
  • Early retinal degeneration (ERD)
  • Generalized progressive retinal atrophy (GPRA)
  • Goniodysgenesis and Glaucoma
  • Primary Lens Luxation (PLL)
  • Primary Open Angle Glaucoma (POAG)
  • Progressive Retinal Atrophy, (PRA), Progressive Retinal Atrophy 1, Progressive Retinal Atrophy III
  • Progressive Rod Cone Degeneration (prcd-PRA)
  • X-Linked Progressive Retinal Atrophy 1 (XLPRA1), X-Linked Progressive Retinal Atrophy 2 (XLPRA2)
  • Rod-Cone Dysplasia 1, Rod-Cone Dysplasia (rcd1a), Rod-Cone Dysplasia 3 (rcd3)

Cardiac Disorders

  • Dilated cardiomyopathy (DCM)
  • Long QT Syndrome (LQTS)

Endocrine Disorders

  • Congenital Dyshormonogenic Hypothyroidism (CDH)
  • Congenital Hypothyroidism

Immunological Disorders

  • Severe Combined Immunodeficiency (ARSCID), Severe Combined Immunodeficiency (SCID)
  • X-linked Severe Combined Immunodeficiency (XSCID)

Renal Disorders

  • 2,8-dihydroxyadenine (DHA) Urolithiasis
  • Renal Cystadenocarcinoma and Nodular Dermatofibrosis (RCND)
  • Protein Losing Nephropathy (PLN)
  • Polycystic Kidney Disease (PKD)
  • Cystinuria Type I-A, Cystinuria Type II-A
  • Cystic Renal Dysplasia and Hepatic Fibrosis
  • Hyperuricosuria, (HUU)

Metabolic Disorders

  • Glycogen Storage Disease Type IIIa, (GSD IIIa), Glycogen Storage Disease Type Ia
  • Intestinal Cobalamin Malabsorption (ICM) or Imerslund-Gräsbeck Syndrome
  • Pyruvate Dehydrogenase Phosphatase 1 (PDP1) Deficiency

Muscular Disorders

  • Muscular Dystrophy
  • Centronuclear Myopathy (CNM)

Neurological Disorders

  • Benign Familial Juvenile Epilepsy (BFJE)
  • Juvenile Myoclonic Epilepsy
  • Juvenile Encephalopathy
  • Neonatal Encephalopathy with Seizures (NEWS)
  • Spongiform LeucoEncephaloMyelopathy (SLEM) (Shaking Puppy Syndrome)
  • Spinocerebellar Ataxia with Myokymia and/or Seizures (SAMS)
  • Degenerative Myelopathy (DM)

Neuromuscular Disorders

  • Congenital Myasthenic Syndrome (CMS)
  • Exercise-Induced Collapse (EIC)
  • GM1 Gangliosidosis, GM2 Gangliosidosis

Skeletal Disorders

  • Chondrodysplasia
  • Cleft Lip & Palate with Syndactyly (CLPS)
  • Cleft Palate (CP)
  • Craniomandibular Osteopathy (CMO)
  • Osteochondrodysplasia
  • Osteogenesis Imperfecta (OI)
  • Hypophosphatasia
  • Skeletal Dysplasia 2 (SD2)
  • Spondylocostal Dysostosis

Dermal Disorders

  • Dystrophic Epidermolysis Bullosa
  • Epidermolytic Hyperkeratosis
  • Ichthyosis
  • Lamellar Ichthyosis, (LI)
  • Lethal Acrodermatitis, (LAD)

Other Disorders

  • Acute respiratory distress syndrome (ARDS)
  • Amelogenesis Imperfecta (AI)
  • Lung Developmental Disease
  • Primary Ciliary Dyskinesia (PCD)
  • MDR1 Medication Sensitivity

Traits

  • Piebald Gene

Non-DNA Testing/Polygenetic Disease

  • Patellas - 0/0 - OFA Testing Form Available

Sire Bedfords Magic Of PationCanine
Dam Bedsy's Maybe She's Bornwithit
GenderFemale
NameDaphne
OwnerBedford Kennel
BreederBedford Kennel

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