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Increasing Hereditary Health Problems in the Breeding of Purebred ...

Increasing Hereditary Health Problems in the Breeding of Purebred ...

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Between 1970 and 1990 <strong>the</strong> Doberman became a voguebreed <strong>in</strong> <strong>the</strong> USA; this resulted <strong>in</strong> mass over-breed<strong>in</strong>g. Thecauses <strong>of</strong> <strong>the</strong> Doberman’s boom were on <strong>the</strong> one hand <strong>the</strong>grow<strong>in</strong>g security need <strong>of</strong> citizens and on <strong>the</strong> o<strong>the</strong>r hand <strong>the</strong>successful advertisement <strong>of</strong> <strong>the</strong> “protector dog” image <strong>of</strong> <strong>the</strong>breed <strong>in</strong> movies. This role was subsequently taken over by <strong>the</strong>Rottweiler and <strong>the</strong> German Shepherd Dog <strong>in</strong> <strong>the</strong> n<strong>in</strong>eties <strong>in</strong> <strong>the</strong>USA. This over-breed<strong>in</strong>g and <strong>in</strong>breed<strong>in</strong>g <strong>of</strong> Dobermans, takentoge<strong>the</strong>r with <strong>in</strong>sufficient attention to <strong>the</strong>ir hereditary health,has resulted <strong>in</strong> a North American Doberman population that ishighly burdened with 5 hereditary defects (Table 1). Thereforewe are forced to acknowledge a strong degeneration <strong>in</strong> <strong>the</strong>breed that might be hard to repair by means <strong>of</strong> conventionalanimal breed<strong>in</strong>g. The population <strong>of</strong> German and Europeandogs is similarly highly burdened with 2 hereditary defects asa consequence <strong>of</strong> <strong>the</strong> same bad breed<strong>in</strong>g practices as <strong>in</strong> <strong>the</strong>USA. The o<strong>the</strong>r 3 hereditary defects are scarcer <strong>in</strong> Europe, butan <strong>in</strong>crease is now apparent!Freya’s daughter, Anka von der Domstadt, SchH1 (born 1972)dur<strong>in</strong>g <strong>the</strong> attackTable 1: Estimated spread <strong>of</strong> 7 degenerative hereditary diseases as well as <strong>the</strong>ir heritability (estimated value <strong>of</strong> geneticvariance <strong>in</strong> <strong>the</strong> total variance) <strong>in</strong> 3 different Doberman populations. The estimates for East European populations aresomewhat more uncerta<strong>in</strong> because an <strong>in</strong>creas<strong>in</strong>g dilution <strong>of</strong> <strong>the</strong> <strong>in</strong>digenous gene pool has taken place as a consequence<strong>of</strong> imports from Western Europe and <strong>the</strong> USA and additionally because <strong>the</strong>re are fewer reliable sourcesSpread <strong>of</strong> hereditary defects <strong>in</strong>:Disease (Symptoms)1. Dilatedcardiomyopathy, DCM(Sudden death andcongestive heart failure)2. Gastric Volvulus(bloat, shock and death)Heritabilityhighmedium tohighMode <strong>of</strong>Inheritancepolygenetic butmostly autosomally(<strong>in</strong>completely)dom<strong>in</strong>ant (partly X-chromosomal)USAvery highWestern Europe(2004)very high, but <strong>in</strong><strong>the</strong> <strong>in</strong>dividual DCMgenotypes, bigdifferencesEasternEurope (1990)littlepolygenetic high high and <strong>in</strong>creas<strong>in</strong>g! little3. Hypothyroidism (sk<strong>in</strong>problems but variouso<strong>the</strong>r severe symptomspossible)very highseveral genes?monogenetic?high little, but <strong>in</strong>creas<strong>in</strong>g! little4. Von-Willebranddisease = VWD(potentially severebleed<strong>in</strong>g)very highautosomally(<strong>in</strong>completely)recessivemonogenetichigh little, but <strong>in</strong>creas<strong>in</strong>g! little5. Wobbler syndrome(paralyses)very highmonogenetic?polygenetic?high1989 little, but after<strong>the</strong>n, fast <strong>in</strong>creas<strong>in</strong>g;2004 mediumlittle6. PHTVL/PHPV (rang<strong>in</strong>gfrom impaired vision tobl<strong>in</strong>dness)highautosomally(<strong>in</strong>completely)dom<strong>in</strong>antlittlelittle to medium(below 15%)little7. Hip jo<strong>in</strong>t dysplasia–HD, (crippl<strong>in</strong>g arthritisand hip pa<strong>in</strong>)medium polygenetic little little (phenotypebelow 5%)little

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