hodowla
Testy zdrowotne
Strona dokumentuje zakres badań zdrowotnych wykonywanych u psów hodowlanych Włochatej Pasji, od stawów po szeroki panel chorób genetycznych.
Badania stawów biodrowych i łokciowychSzeroki panel chorób genetycznychŚwiadome parowanie psów hodowlanych
Australijski Labradoodle a testy zdrowotne
Australijski Labradoodle a testy zdrowotne. Oto choroby na które testujemy nasze psy:
główne
Główne badania i choroby
- Dysplazja stawów biodrowych i łokciowych (FCI standards)
- Improper Coat
- Von Willebrand Disease Type I, Type I vWD (VWF)
- Canine Elliptocytosis (SPTB Exon 30)
- Pyruvate Kinase Deficiency (PKLR Exon 7, Labrador Retriever Variant)
- Progressive Retinal Atrophy, prcd (PRCD Exon 1)
- Golden Retriever Progressive Retinal Atrophy 2, GR-PRA2 (TTC8)
- Progressive Retinal Atrophy, crd4/cord1 (RPGRIP1)
- Achromatopsia (CNGA3 Exon 7, Labrador Retriever Variant)
- Macular Corneal Dystrophy, MCD (CHST6)
- Hyperuricosuria and Hyperuricemia or Urolithiasis, HUU (SLC2A9)
- Congenital Keratoconjunctivitis Sicca and Ichthyosiform Dermatosis, Dry Eye Curly Coat Syndrome, CKCSID (FAM83H Exon 5)
- GM2 Gangliosidosis (HEXB, Poodle Variant)
- Alexander Disease (GFAP)
- Degenerative Myelopathy, DM (SOD1A)
- Neonatal Encephalopathy with Seizures, NEWS (ATF2)
- Narcolepsy (HCRTR2 Intron 6, Labrador Retriever Variant)
- Muscular Dystrophy (DMD, Cavalier King Charles Spaniel Variant 1)
- Ullrich-like Congenital Muscular Dystrophy (COL6A3 Exon 10, Labrador Retriever Variant)
- Centronuclear Myopathy, CNM (PTPLA)
- Exercise-Induced Collapse, EIC (DNM1)
- Myotubular Myopathy 1, X-linked Myotubular Myopathy, XL-MTM (MTM1, Labrador Retriever Variant)
pozostałe
Pozostałe badania
- MDR1 Drug Sensitivity (ABCB1)
- P2Y12 Receptor Platelet Disorder (P2Y12)
- Factor IX Deficiency, Hemophilia B variants
- Factor VII Deficiency (F7 Exon 5)
- Factor VIII Deficiency, Hemophilia A variants
- Thrombopathia variants
- Von Willebrand Disease Type III and Type II variants
- Canine Leukocyte Adhesion Deficiency Type I and III
- Congenital Macrothrombocytopenia
- Glanzmann's Thrombasthenia Type I variants
- May-Hegglin Anomaly (MYH9)
- Prekallikrein Deficiency (KLKB1 Exon 8)
- Pyruvate Kinase Deficiency variants
- Trapped Neutrophil Syndrome, TNS
- Ligneous Membranitis, LM
- Platelet Factor X Receptor Deficiency, Scott Syndrome
- Methemoglobinemia (CYB5R3)
- Congenital Hypothyroidism variants
- Complement 3 Deficiency, C3 Deficiency
- Severe Combined Immunodeficiency and X-linked Severe Combined Immunodeficiency variants
- Progressive Retinal Atrophy variants including rcd1, rcd3, CNGA, PRA1, SAG, GR-PRA1, crd1, XL-PRA1 and PRA3
- Collie Eye Anomaly, Choroidal Hypoplasia, CEA
- Day Blindness, Cone Degeneration and Achromatopsia variants
- Autosomal Dominant Progressive Retinal Atrophy (RHO)
- Canine Multifocal Retinopathy variants
- Primary Open Angle Glaucoma and Primary Lens Luxation variants
- Goniodysgenesis and Glaucoma, Pectinate Ligament Dysplasia, PLD
- Hereditary Cataracts, Early-Onset Cataracts, Juvenile Cataracts
- Congenital Stationary Night Blindness variants
- 2,8-Dihydroxyadenine Urolithiasis, 2,8-DHA Urolithiasis
- Cystinuria Type I-A, II-A and II-B
- Polycystic Kidney Disease, PKD
- Primary Hyperoxaluria and Protein Losing Nephropathy, PLN
- X-Linked Hereditary Nephropathy, XLHN
- Autosomal Recessive Hereditary Nephropathy, Familial Nephropathy, ARHN
- Primary Ciliary Dyskinesia variants
- X-linked Ectodermal Dysplasia, Anhidrotic Ectodermal Dysplasia, XHED
- Renal Cystadenocarcinoma and Nodular Dermatofibrosis, RCND
- Canine Fucosidosis
- Glycogen Storage Disease variants including GSD II, IA, IIIA and VII
- Mucopolysaccharidosis variants including MPS IIIA and MPS VII
- Lagotto Storage Disease (ATG4D)
- Neuronal Ceroid Lipofuscinosis variants
- GM1 and GM2 Gangliosidosis variants
- Globoid Cell Leukodystrophy, Krabbe disease
- Autosomal Recessive Amelogenesis Imperfecta, Familial Enamel Hypoplasia
- Persistent Mullerian Duct Syndrome, PMDS
- Deafness and Vestibular Syndrome of Dobermans, DVDob, DINGS
- Shar-Pei Autoinflammatory Disease, SPAID, Shar-Pei Fever
- Neonatal Interstitial Lung Disease
- Alaskan Husky Encephalopathy
- Cerebellar Abiotrophy, Cerebellar Ataxia and Cerebellar Hypoplasia variants
- Spinocerebellar Ataxia variants
- Hereditary Ataxia, Cerebellar Degeneration
- Benign Familial Juvenile Epilepsy
- Fetal-Onset Neonatal Neuroaxonal Dystrophy
- Hypomyelination and Tremors
- Shaking Puppy Syndrome, X-linked Generalized Tremor Syndrome
- Neuroaxonal Dystrophy variants
- L-2-Hydroxyglutaricaciduria, L2HGA
- Alaskan Malamute Polyneuropathy, AMPN
- Narcolepsy variants
- Progressive Neuronal Abiotrophy, Canine Multiple System Degeneration
- Juvenile Laryngeal Paralysis and Polyneuropathy
- Hereditary Sensory Autonomic Neuropathy, Acral Mutilation Syndrome
- Sensory Neuropathy
- Juvenile-Onset Polyneuropathy and Leonberger Polyneuropathy variants
- Juvenile Myoclonic Epilepsy
- Spongy Degeneration with Cerebellar Ataxia variants
- Dilated Cardiomyopathy variants
- Long QT Syndrome and Cardiomyopathy and Juvenile Mortality
- Muscular Dystrophy and Limb Girdle Muscular Dystrophy variants
- Inherited Myopathy of Great Danes
- Myostatin Deficiency, Bully Whippet Syndrome
- Myotonia Congenita variants
- Inflammatory Myopathy and Hypocatalasia, Acatalasemia
- Pyruvate Dehydrogenase Deficiency
- Malignant Hyperthermia
- Imerslund-Grasbeck Syndrome variants
- Inherited Selected Cobalamin Malabsorption with Proteinuria
- Lundehund Syndrome
- Congenital Myasthenic Syndrome variants
- Myasthenia Gravis-Like Syndrome
- Paroxysmal Dyskinesia, PxD
- Demyelinating Polyneuropathy
- Dystrophic Epidermolysis Bullosa variants
- Ectodermal Dysplasia, Skin Fragility Syndrome
- Ichthyosis variants
- Hereditary Footpad Hyperkeratosis variants
- Musladin-Lueke Syndrome, MLS
- Oculocutaneous Albinism, OCA
- Bald Thigh Syndrome
- Lethal Acrodermatitis, LAD
- Ehlers Danlos
- Cleft Lip and/or Cleft Palate
- Hereditary Vitamin D-Resistant Rickets
- Osteogenesis Imperfecta variants
- Craniomandibular Osteopathy, CMO
- Raine Syndrome, Canine Dental Hypomineralization Syndrome
- Chondrodystrophy
wejdź do świata Labradoodle.pl
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