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rel="nofollow" href="http://bit.ly/2YWXBsc">http://bit.ly/2YWXBsc or https://dogwellnet.com/ctp). Of course, mistakes do happen. In this instance, the most likely cause for pups testing “affected” for prcd when the parents tested “clear” would be that the breeders made a mistake in identifying which animals were the actual parents. Theoretically, it would also be possible that the pups developed a spontaneous mutation, but this is very rare.
Table 3.11.1 Some of the genotypic tests currently available
| 2,8‐Dihydroxyadenine Urolithiasis Type IA |
| Achromatopsia |
| Acral Mutilation Syndrome |
| Acute Respiratory Distress Syndrome |
| Aggression (markers) |
| Alanine Aminotransferase (ALT) Activity |
| Alexander Disease |
| Amelogenesis Imperfecta |
| Arrhythmogenic Right Ventricular Cardiomyopathy |
| Autoimmune lymphoproliferative Syndrome |
| Bardet–Biedl Syndrome |
| Bernard Soulier Syndrome |
| Brain Hypomyelination |
| Burmese Head Defect |
| Canine Leukocyte Adhesion Deficiency Types I & III |
| Canine Multifocal Retinopathy (CMR 1, 2 & 3) |
| Canine Multiple System Degeneration |
| Cardiomyopathy, Dilated (DCM1 and DCM2) |
| Cardiomyopathy, Hypertrophic |
| Catalase Deficiency |
| Centronuclear Myopathy |
| Cerebellar Ataxia |
| Cerebellar Cortical Degeneration |
| Cerebellar Hypoplasia |
| Cerobellar Abiotrophy |
| Chondrodysplasia |
| Chondrodystrophy and intervertebral Disc Disease |
| Ciliary Dyskinesia |
| Cleft Lip with Syndactyly |
| Cleft Lip/Palate |
| Cobalamin Malabsorption |
| Collie Eye Anomaly/Choroidal Hypoplasia |
| Color Dilution Alopecia |
| Complement 3 (C3) deficiency |
| Cone Degeneration |
| Cone‐Rod Dystrophy (1, 2, 3, 4, SWD) |
| Congenital Hypothyroidism with Goiter |
| Congenital Keratoconjunctivities Sicca and Ichthyosiform Dermatosis |
| Congenital Macrothrombocytopenia |
| Congenital Myasthenic Syndrome |
| Congenital Stationary Night Blindness |
| Copper Toxicosis |
| Craniomandibular Osteopathy |
| Curly Coat Dry Eye Syndrome |
| Cyclic Hematopoiesis |
| Cyclic Neutropenia |
| Cystic renal Dysplasia and Hepatic Fibrosis |
| Cystinuria (Types I‐A, II‐A, II‐B) |
| Dandy–Walker Malformation |
| Day Blindess |
| Deafness and Vestibular Syndrome |
| Degenerative Myelopathy |
| Dental Hypomineralization |
| Dermatomyositis |
| Dystrophic Epidermolysis Bullosa |
| Early Adult Onset Deafness |
| Early Onset Progressive Polyneuropathy |
| Ectodermal Dysplasia |
| Elliptocytosis |
| Encephalopathy |
| Epidermolysis Bullosa Simplex |
| Epidermolytic Hyperkeratosis |
| Epilepsy (variants) |
| Episodic Falling Syndrome |
| Exercise‐Induced Collapse |
| Exercise‐Induced Metabolic Myopathy |
| Factor IX Deficiency (Hemophilia B) |
| Factor VII Deficiency |
| Factor VIII Deficiency (Hemophilia A) |
| Factor XI Deficiency |
| Factor XII Deficiency |
| Familial Congenital Methemoglobinemia |
| Familial Juvenile Epilepsy |
| Familial Nephropathy |
| Fanconi Syndrome |
| Fucosidosis |
| Gall Bladder Mucocele Formation |
| Gangliosidosis (GM1 & GM2) |
| Generalized Myoclonic Epilepsy |
| Glanzmann's Thrombasthenia |
| Glaucoma |
| Globoid Cell Leukodystrophy/Krabbe’s Disease |
| Glomerulopathy KIRREL2 |
| Glycogen Storage Disease IA, II, III, IIIA |
| Goniodysgenesis and Glaucoma |
| Hereditary Ataxia |
| Hereditary Cataracts |
| Hereditary Deafness (PTPRQ) |
| Hereditary Footpad Hyperkeratosis |
| Hereditary Nasal Parakeratosis |
| Hereditary Nephropathy |
| Hereditary Nephropathy (Alport Syndrome) |
| Hip Dysplasia (markers) |
