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Home   News and offers   Genetic Diseases Dogs Cats Horses Cattle Pigs Rabbit Sheep   Coat Colours / Length   Identity / Parentage   Reptiles & Amphibians   Avian Tests   Profiles / Screening   Infectious Diseases   Organs / Parameters   Allergy testing   Pathology   Downloads & Order   Order Kit Online   About Us   Crufts & Shows   Contact Us   Kennel Club ABS   facebook   **NEW** Maine Coon Special offer: 8 DNA tests for just £84.95 incl VAT Maine Coon 8 DNA tests bundle (HCM, SMA, PKDef, Poly, b, b1, cb, cs)  **NEW** Bengal Special offer: 4 Bengal Specific DNA tests for just £72.00 incl VAT Bengal DNA bundle (rdAc-PRA + b-PRA + PK-Def + Blood Groups)  British Special offer: 4 Breed Specific DNA tests for just £72.00 incl VAT British Short / Long Hair DNA bundle (PKD + pd-PRA + ALS + Blood Groups) Burmese Special offer: 4 Breed Specific DNA tests for just £72.00 incl VAT Burmese DNA bundle (Hypokalemia (BHK) + Head Defect + Gangliosidosis (GM2) + Blood Groups Birman Special offer: 5 Breed Specific DNA tests for just £72.00 incl VAT Birma DNA bundle (PKD + pd-PRA + Hypotrichiose + MPS6 + Blood Groups) Maine Coon Special offer: 5 Breed Specific DNA tests for just £72.00 incl VAT Maine Coon DNA bundle (HCM1 + SMA + PK-Def + F11 + Blood Groups) Ragdoll Special offer: 5 Breed Specific DNA tests for just £72.00 incl VAT Ragdoll DNA bundle (HCM1 + HCM3 + PKD + pd-PRA + Blood Groups) Norwegian Special offer: 4 Breed Specific DNA tests for just £72.00 incl VAT Norwegian Forest DNA bundle (PK-Def + Amber + GSD4 + Blood Groups) Feline Special Offer: 8 cat DNA tests for just £84.95 including VAT HCM, HCR, GSD4, PKD, PRA, PK-Def., SMA, Blood Groups

new test:      Paradoxical Pseudomyotonia (PP) in English Cocker and English Springer Spaniels   new test:      Dyserythropoietic Anemia and Myopathy Syndrome (DAMS) in English Springer Spaniel new test:      Lysosomal Storage Diseases (LSD) in Dalmatian and Doberman   new Kennel Club DNA testing schemes with LABOKLIN:    • Osteochondrodysplasia (OCD) / Skeletal Dwarfism in Miniature Poodles    • DINGS2: Deafness with Vestibular Dysfunction in Doberman    • Dyserythropoietic Anemia and Myopathy Syndrome (DAMS) in English Springer Spaniel Acrodermatitis enteropathica in Felis catus Test number: 8763 Gene: AE Price: £ 48.00 (including VAT) Breed Turkish Van . The Disease Acrodermatitis Enteropathica ( AE ) is an inherited disease that has been reported in the Turkish Van cat breed. The disease was characterised by severe signs of skin disease, diarrhea, and systemic signs of stunted growth at 6 weeks of age. Massive secondary infections of the skin lesions evolved. Histopathological examinations showed a mild to moderate hyperplastic epidermis, covered by a thick layer of laminar to compact, mostly parakeratotic keratin. The dermis was infiltrated with moderate amounts of lymphocytes and plasma cells. Description The disease is caused by a mutation in the SLC39A4 gene Trait of Inheritance Autosomal recessive mode of inheritance Inheritance : AUTOSOMAL RECESSIVE trait   Sire   Dam   Offspring           clear clear 100% clear           clear carrier 50%  clear + 50% carriers           clear affected 100% carriers           carrier clear 50%  clear + 50% carriers           carrier carrier 25% clear + 25% affected + 50% carriers           carrier affected 50% carriers + 50% affected           affected clear 100%  carriers           affected carrier 50% carriers + 50% affected           affected affected 100% affected   Clear Genotype: N / N [ Homozygous normal ] The cat is noncarrier of the mutant gene. It is very unlikely that the cat will develop Acrodermatitis enteropathica in Felis catus. The cat will never pass the mutation to its offspring, and therefore it can be bred to any other cat.   Carrier Genotype: N / AE [ Heterozygous ] The cat carries one copy of the mutant gene and one copy of the normal gene. It is very unlikely that the cat will develop Acrodermatitis enteropathica in Felis catus but since it carries the mutant gene, it can pass it on to its offspring with the probability of 50%. Carriers should only be bred to clear cats. Avoid breeding carrier to carrier because 25% of their offspring is expected to be affected (see table above)   Affected Genotype: AE / AE [ Homozygous mutant ]   The cat carries two copies of the mutant gene and therefore it will pass the mutant gene to its entire offspring. The cat is likely to develop Acrodermatitis enteropathica in Felis catus and will pass the mutant gene to its entire offspring Sample Requirements Buccal Swabs or 0.5 - 1 ml blood in EDTA Blood Tube Turnaround 1-3 weeks Price £ 48.00 (including VAT) To order: Download Order Form from this link Complete the order form and send it together with your samples to the following address: Laboklin (UK),   Unit 20, Wheel Forge Way, Trafford Park, Manchester, M17 1EH Buccal swabs and EDTA tubes are available from us free of charge, to order, please use the online form <Request sample collection materials> or  email: info@laboklin.co.uk. If you are sending swab samples, please follow the instructions on this link . If you have any queries, please contact us on 0161 282 3066 new test: Androgen Insensitivity Syndrome (AIS) new test: ACAN Dwarfism (Chondrodysplasia) new test: Predictive Height Test ( LCORL) new test: Tractability new test: Coat colour Sunshire Dilution See also: HCM 1 (Hypertrophic Cardiomyopathy) Osteochondrodysplasia (Scottish Fold Osteodystrophy) OCD HCM (Hypertrophic Cardiomyopathy HCM3/HCR) PKD (Feline Polycystic Kidney Disease) PK Deficiency (Pyruvate Kinase Deficiency) Progressive Retinal Atrophy ( rdAc - PRA ) SMA (Spinal Muscular Atrophy ) Serological Evaluation of blood Groups Hypokalemia / Familial Episodic Hypokalaemic Polymyopathy (BHK) Head Defect (BHD) Alpha-Mannosidosis (AMD) Congenital Myasthenic Syndrome (CMS) / Hereditary Myopathy Gangliosidosis GM1 Gangliosidosis GM2 Gangliosidosis GM2 Mucopolysaccharidosis Type VI (MPS VI MPS6) Mucopolysaccharidosis type VII (MPS VII / MPS7) Myotonia Congenita (Fainting Goat) Progressive Retinal Atrophy (pd-PRA) Progressive Retinal Atrophy (rdy-PRA) Hypotrichosis and Short Life Expectancy Progressive Retinal Atrophy in Bengal (PRA-b / b-PRA) Special Offer: HCM, HCR, GSD4, PKD, PRA, PK-Def., SMA, Blood Groups Primary Congenital Glaucoma (PCG) Cystinuria (Feline Cystinuria) (CY) Persian DNA bundle (PKD + pd-PRA + AMD + Blood Groups) British Short / Long Hair DNA bundle (PKD + pd-PRA + ALPS + Blood Groups) Burmese DNA bundle (Hypokalemia (BHK) + Head Defect + Gangliosidosis (GM2) + Blood Groups Birma DNA bundle (PKD + pd-PRA + Hypotrichiose + MPS6 + Blood Groups) Bengal DNA bundle (rdAc-PRA + b-PRA + PK-Def + Blood groups) Maine Coon DNA bundle (HCM1 + SMA + PK-Def + FXI + Blood Groups) Ragdoll DNA bundle (HCM1 + HCM3 + PKD + pd-PRA + Blood groups) Norwegian Forest DNA bundle (PK-Def + Amber + GSD4 + Blood groups) Siamese / Oriental DNA bundle (GM1 + MPS6 + PCG + rdAc-PRA + Blood Groups) Sphynx DNA bundle (HCM4 + Hypokalemia + CMS + Blood groups) Factor XI deficiency ( F11 ) MDR1 Gene Defect Skeletal Dysplasia Factor 12 FXII cat Devon Rex DNA bundle (CMS + Blood Groups + Long Coat + Rex Hair) Siberian DNA Bundle (Blood Groups + PK-Def + Dilution + Colourpoint) Genetic Blood groups in cats LABOGenetics XXL Cat - Comprehensive Feline DNA bundle Autoimmune Lymphoproliferative Syndrome (ALPS) Polydactyly (extra toes) / polydactylism / Polydactyl / hyperdactyly Unlisted DNA test Congenital Hypothyroidism (CH) Maine Coon 8 DNA tests bundle (HCM, SMA, PKDef, Poly, b, b1, cb, cs) Blue Eyes HCM4 ( Hypertrophic Cardiomyopathy HCM 4) in Sphynx Polycystic Kidney Disease 2 (PKD2) Glycogen Storage Disease ( GSD ) Type IV

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