Dalmatische Hond

FCI Groep: 6
Oordeel: zeer hoog risico op erfelijke aandoeningen
Bij dit ras voorkomende, erfelijke aandoeningen:Uitleg
Bronnen:
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- Gough, A. en Thomas, A. (2004) Breed Predispositions to Disease in Dogs and Cats. Oxford: Blackwell Publishing Ltd
- W.K.Hirschfeldstichting (WKHS), Raad van Beheer op kynologisch Gebied (RvB), Genetic Counselling Services (GCS): Gezondheidsinventarisaties periode 1995-2010. www.gencouns.nl
- LICG (2011) Erfelijke aandoeningen bij honden. Utrecht: Universiteit Utrecht
- Orthopedic Foundation for Animals (2011) Hip Dysplasia Statistics. Breeds having at least 100 evaluations January 1974 through December 2010. Columbia, Missouri: OFFA. www.offa.org
- Roberts , T. en McGreevy, P.D. (2010) Selection for breed-specific longbodied phenotypes is associated with increased expression of canine hip dysplasia. The Veterinary Journal 183 (2010) 266-272
- Orthopedic Foundation for Animals (2011) Elbow Dysplasia Statistics. Breeds having at least 100 evaluations January 1974 through December 2010. Columbia, Missouri: OFFA. www.offa.org
- Gelatt, K.N. En MacKay, E.D. (2005) Prevalence of primary breed-related cataracts in the dog in North America. Veterinary Ophthalmology 8, 2, 101-111
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- Bavegems, V. (2006) Erfelijke hartaandoeningen bij de hond. Gent: Universiteit Gent, Diergeneeskunde.
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- Speth RC.(2010) Re: Inheritance of urinary calculi in the Dalmatian. J Vet Intern Med. 24(6):1239-40.
- Persoonlijke communicatie Universiteit Utrecht, Faculteit Diergeneeskunde, 2011
- Strain GM. (2004) Deafness prevalence and pigmentation and gender associations in dog breeds at risk. Vet J. 167(1):23-32
- Mieskes K, Distl O. (2007) Evaluation of ESPN, MYO3A, SLC26A5 and USH1C as candidates for hereditary non-syndromic deafness (congenital sensorineural deafness) in Dalmatian dogs. Anim Genet. 38(5):533-4.
- Stritzel S, Wöhlke A, Distl O. (2009) A role of the microphthalmia-associated transcription factor in congenital sensorineural deafness and eye pigmentation in Dalmatian dogs. J Anim Breed Genet. 2009 Feb;126(1):59-62.



