CRB'S COUNT CHOCULA @ JCF
Count is now available to a local, very approved home. He's a very special guy and we love him dearly, making this decision very difficult.
He's excellent with people of all ages, female dogs, some male dogs, and tolerates cats. Very house trained, walks well on a leash, and does not chew up random items. He cannot go to a home with smaller livestock (chickens, waterfowl, goats, etc), although horses are okay.
He has been neutered, and is up to date on DHA2PP (parvo, distemper, etc) and his rabies vaccine.
~*~
Count comes to us from Canada! A huge thanks to Sandi of Boss Kennel Rottiebears for this wonderful dog. We're extremely excited to have him!
Count brings new, unrelated bloodlines to our program. I love his extra-laid back disposition, nice topline, good bone, and good muzzle shape. The chocolate color is the icing on the cake.
He's excellent with people of all ages, female dogs, some male dogs, and tolerates cats. Very house trained, walks well on a leash, and does not chew up random items. He cannot go to a home with smaller livestock (chickens, waterfowl, goats, etc), although horses are okay.
He has been neutered, and is up to date on DHA2PP (parvo, distemper, etc) and his rabies vaccine.
~*~
Count comes to us from Canada! A huge thanks to Sandi of Boss Kennel Rottiebears for this wonderful dog. We're extremely excited to have him!
Count brings new, unrelated bloodlines to our program. I love his extra-laid back disposition, nice topline, good bone, and good muzzle shape. The chocolate color is the icing on the cake.
Count at ~ 1 year old.
Count at ~7 months.
Count at ~3 months.
Count's health test results:
OFA Certificates:
DNA Testing:
Count's parents have been tested with a comprehensive panel offered by Canine Health Check (a division of Paw Print Genetics), and was found clear for the below genetic mutations. This means Count is 'clear by parentage,' and does not need to be tested himself.
Sire: Brodie Apollo Boss (click here for test results)
Dam: Cassie Rhea Boss (click here for test results)
Disease testing included in this panel:
Adult-onset neuronal ceroid lipofuscinosis
Alaskan Husky encephalopathy
Alaskan Malamute polyneuropathy
Amelogenesis imperfecta
Anhidrotic ectodermal dysplasia
Benign familial juvenile epilepsy
Canine multiple system degeneration (Chinese Crested type)
Canine multiple system degeneration (Kerry Blue Terrier type)
Cerebellar ataxia (Finnish Hound type)
Chondrodysplasia
Coagulation factor VII deficiency
Collie eye anomaly
Complement 3 deficiency
Cone degeneration
Cone degeneration (German Shorthaired Pointer type)
Congenital hypothyroidism with goiter (Terrier type)
Congenital myasthenic syndrome
Congenital myasthenic syndrome (Labrador Retriever type)
Congenital stationary night blindness
Cyclic neutropenia
Cystinuria (Australian Cattle Dog type)
Cystinuria (Miniature Pinscher type)
Cystinuria (Newfoundland type)
Degenerative myelopathy
Dilated cardiomyopathy
Dry eye curly coat syndrome
Dystrophic epidermolysis bullosa
Early retinal degeneration
Ectodermal dysplasia
Elliptocytosis
Epidermolytic hyperkeratosis
Episodic falling syndrome
Exercise-induced collapse
Familial nephropathy (Cocker Spaniel type)
Familial nephropathy (English Springer Spaniel type)
Fanconi syndrome
Gallbladder mucoceles
Glanzmann's thrombasthenia (Great Pyrenees type)
Glanzmann's thrombasthenia (Otterhound type)
Globoid cell leukodystrophy (Irish Setter type)
Globoid cell leukodystrophy (Terrier type)
Glycogen storage disease Ia
Glycogen storage disease IIIa
Glycogen storage disease VII (Wachtelhund type)
GM1 Gangliosidosis (Alaskan Husky type)
GM1 Gangliosidosis (Portuguese Water Dog type)
GM1 Gangliosidosis (Shiba Inu type)
GM2 Gangliosidosis (Japanese Chin type)
GM2 Gangliosidosis (Poodle type)
Golden Retriever muscular dystrophy
Greyhound polyneuropathy
Hemophilia A
Hemophilia A (Boxer type)
Hemophilia A (German Shepherd Dog, type 1)
Hemophilia B (Cairn Terrier type)
Hemophilia B (Lhasa Apso type)
Hemophilia B (Rhodesian Ridgeback type)
Hereditary cataracts
Hereditary cataracts (Australian Shepherd type)
Hereditary footpad hyperkeratosis (Irish Terrier and Kromfohrländer type)
Hereditary nasal parakeratosis
Hereditary nephritis (Samoyed type)
Hyperuricosuria
Ichthyosis (Golden Retriever type)
Inherited myopathy of Great Danes
Intestinal cobalamin malabsorption (Beagle type)
Intestinal cobalamin malabsorption (Border Collie type)
L-2-hydroxyglutaric aciduria (Staffordshire Bull Terrier type)
Late onset ataxia
Leukocyte adhesion deficiency, type I
Leukocyte adhesion deficiency, type III
May-Hegglin anomaly
Mucopolysaccharidosis I
Mucopolysaccharidosis IIIA (Dachshund type)
Mucopolysaccharidosis IIIA (New Zealand Huntaway type)
Mucopolysaccharidosis VII (Shepherd type)
Multidrug resistance 1
Multifocal retinopathy 1
Multifocal retinopathy 2
Multifocal retinopathy 3
Musladin-Lueke syndrome
Myostatin deficiency (Whippet and Longhaired Whippet type)
Myotonia congenita (Australian Cattle Dog type)
Myotonia congenita (Schnauzer type)
Myotubular myopathy 1
Narcolepsy (Dachshund type)
Narcolepsy (Doberman Pinscher type)
Narcolepsy (Labrador Retriever type)
Neonatal cerebellar cortical degeneration
Neonatal encephalopathy with seizures
Neuronal ceroid lipofuscinosis 1
Neuronal ceroid lipofuscinosis 10
Neuronal ceroid lipofuscinosis 2
Neuronal ceroid lipofuscinosis 4A
Neuronal ceroid lipofuscinosis 5
Neuronal ceroid lipofuscinosis 6
Neuronal ceroid lipofuscinosis 8
Neuronal ceroid lipofuscinosis 8 (Australian Shepherd type)
Osteochondrodysplasia
Osteogenesis imperfecta (Beagle type)
Osteogenesis imperfecta (Dachshund type)
Osteogenesis imperfecta (Golden Retriever type)
P2RY12 receptor platelet disorder
Pembroke Welsh Corgi Duchenne muscular dystrophy
Persistent Müllerian duct syndrome
Polyneuropathy (Leonberger and Saint Bernard type)
Pompe disease
Prekallikrein deficiency
Primary ciliary dyskinesia
Primary hyperoxaluria
Primary lens luxation
Primary open angle glaucoma
Progressive retinal atrophy (Basenji type)
Progressive retinal atrophy (Bullmastiff/Mastiff type)
Progressive retinal atrophy (Irish Setter type)
Progressive retinal atrophy (Sloughi type)
Progressive retinal atrophy, Cone-rod dystrophy 1
Progressive retinal atrophy, Cone-rod dystrophy 2
Progressive retinal atrophy, Cone-rod dystrophy 3
Progressive retinal atrophy, generalized
Progressive retinal atrophy, Golden Retriever 2
Progressive retinal atrophy, PRA1 (Papillon type)
Progressive retinal atrophy, Progressive rod-cone degeneration
Progressive retinal atrophy, Rod-cone dysplasia 3
Pyruvate dehydrogenase deficiency
Pyruvate kinase deficiency (Basenji type)
Pyruvate kinase deficiency (Beagle type)
Pyruvate kinase deficiency (Labrador Retriever type)
Pyruvate kinase deficiency (Pug type)
Pyruvate kinase deficiency (Terrier type)
Renal cystadenocarcinoma and nodular dermatofibrosis
Sensory ataxic neuropathy
Severe combined immunodeficiency disease (Terrier type)
Severe combined immunodeficiency disease (Wetterhoun type)
Severe combined immunodeficiency disease, X-linked (Basset Hound type)
Severe combined immunodeficiency disease, X-linked (Corgi type)
Skeletal dysplasia 2
Spinal dysraphism (Weimaraner type)
Spinocerebellar ataxia
Startle disease
Thrombopathia (American Eskimo Dog type)
Thrombopathia (Basset Hound type)
Thrombopathia (Newfoundland type)
Trapped neutrophil syndrome
Vitamin D dependent rickets, type II
Von Willebrand disease I
Von Willebrand disease II
Testing performed prior to receiving his parents' results:
Count's parents have been tested with a comprehensive panel offered by Canine Health Check (a division of Paw Print Genetics), and was found clear for the below genetic mutations. This means Count is 'clear by parentage,' and does not need to be tested himself.
Sire: Brodie Apollo Boss (click here for test results)
Dam: Cassie Rhea Boss (click here for test results)
Disease testing included in this panel:
Adult-onset neuronal ceroid lipofuscinosis
Alaskan Husky encephalopathy
Alaskan Malamute polyneuropathy
Amelogenesis imperfecta
Anhidrotic ectodermal dysplasia
Benign familial juvenile epilepsy
Canine multiple system degeneration (Chinese Crested type)
Canine multiple system degeneration (Kerry Blue Terrier type)
Cerebellar ataxia (Finnish Hound type)
Chondrodysplasia
Coagulation factor VII deficiency
Collie eye anomaly
Complement 3 deficiency
Cone degeneration
Cone degeneration (German Shorthaired Pointer type)
Congenital hypothyroidism with goiter (Terrier type)
Congenital myasthenic syndrome
Congenital myasthenic syndrome (Labrador Retriever type)
Congenital stationary night blindness
Cyclic neutropenia
Cystinuria (Australian Cattle Dog type)
Cystinuria (Miniature Pinscher type)
Cystinuria (Newfoundland type)
Degenerative myelopathy
Dilated cardiomyopathy
Dry eye curly coat syndrome
Dystrophic epidermolysis bullosa
Early retinal degeneration
Ectodermal dysplasia
Elliptocytosis
Epidermolytic hyperkeratosis
Episodic falling syndrome
Exercise-induced collapse
Familial nephropathy (Cocker Spaniel type)
Familial nephropathy (English Springer Spaniel type)
Fanconi syndrome
Gallbladder mucoceles
Glanzmann's thrombasthenia (Great Pyrenees type)
Glanzmann's thrombasthenia (Otterhound type)
Globoid cell leukodystrophy (Irish Setter type)
Globoid cell leukodystrophy (Terrier type)
Glycogen storage disease Ia
Glycogen storage disease IIIa
Glycogen storage disease VII (Wachtelhund type)
GM1 Gangliosidosis (Alaskan Husky type)
GM1 Gangliosidosis (Portuguese Water Dog type)
GM1 Gangliosidosis (Shiba Inu type)
GM2 Gangliosidosis (Japanese Chin type)
GM2 Gangliosidosis (Poodle type)
Golden Retriever muscular dystrophy
Greyhound polyneuropathy
Hemophilia A
Hemophilia A (Boxer type)
Hemophilia A (German Shepherd Dog, type 1)
Hemophilia B (Cairn Terrier type)
Hemophilia B (Lhasa Apso type)
Hemophilia B (Rhodesian Ridgeback type)
Hereditary cataracts
Hereditary cataracts (Australian Shepherd type)
Hereditary footpad hyperkeratosis (Irish Terrier and Kromfohrländer type)
Hereditary nasal parakeratosis
Hereditary nephritis (Samoyed type)
Hyperuricosuria
Ichthyosis (Golden Retriever type)
Inherited myopathy of Great Danes
Intestinal cobalamin malabsorption (Beagle type)
Intestinal cobalamin malabsorption (Border Collie type)
L-2-hydroxyglutaric aciduria (Staffordshire Bull Terrier type)
Late onset ataxia
Leukocyte adhesion deficiency, type I
Leukocyte adhesion deficiency, type III
May-Hegglin anomaly
Mucopolysaccharidosis I
Mucopolysaccharidosis IIIA (Dachshund type)
Mucopolysaccharidosis IIIA (New Zealand Huntaway type)
Mucopolysaccharidosis VII (Shepherd type)
Multidrug resistance 1
Multifocal retinopathy 1
Multifocal retinopathy 2
Multifocal retinopathy 3
Musladin-Lueke syndrome
Myostatin deficiency (Whippet and Longhaired Whippet type)
Myotonia congenita (Australian Cattle Dog type)
Myotonia congenita (Schnauzer type)
Myotubular myopathy 1
Narcolepsy (Dachshund type)
Narcolepsy (Doberman Pinscher type)
Narcolepsy (Labrador Retriever type)
Neonatal cerebellar cortical degeneration
Neonatal encephalopathy with seizures
Neuronal ceroid lipofuscinosis 1
Neuronal ceroid lipofuscinosis 10
Neuronal ceroid lipofuscinosis 2
Neuronal ceroid lipofuscinosis 4A
Neuronal ceroid lipofuscinosis 5
Neuronal ceroid lipofuscinosis 6
Neuronal ceroid lipofuscinosis 8
Neuronal ceroid lipofuscinosis 8 (Australian Shepherd type)
Osteochondrodysplasia
Osteogenesis imperfecta (Beagle type)
Osteogenesis imperfecta (Dachshund type)
Osteogenesis imperfecta (Golden Retriever type)
P2RY12 receptor platelet disorder
Pembroke Welsh Corgi Duchenne muscular dystrophy
Persistent Müllerian duct syndrome
Polyneuropathy (Leonberger and Saint Bernard type)
Pompe disease
Prekallikrein deficiency
Primary ciliary dyskinesia
Primary hyperoxaluria
Primary lens luxation
Primary open angle glaucoma
Progressive retinal atrophy (Basenji type)
Progressive retinal atrophy (Bullmastiff/Mastiff type)
Progressive retinal atrophy (Irish Setter type)
Progressive retinal atrophy (Sloughi type)
Progressive retinal atrophy, Cone-rod dystrophy 1
Progressive retinal atrophy, Cone-rod dystrophy 2
Progressive retinal atrophy, Cone-rod dystrophy 3
Progressive retinal atrophy, generalized
Progressive retinal atrophy, Golden Retriever 2
Progressive retinal atrophy, PRA1 (Papillon type)
Progressive retinal atrophy, Progressive rod-cone degeneration
Progressive retinal atrophy, Rod-cone dysplasia 3
Pyruvate dehydrogenase deficiency
Pyruvate kinase deficiency (Basenji type)
Pyruvate kinase deficiency (Beagle type)
Pyruvate kinase deficiency (Labrador Retriever type)
Pyruvate kinase deficiency (Pug type)
Pyruvate kinase deficiency (Terrier type)
Renal cystadenocarcinoma and nodular dermatofibrosis
Sensory ataxic neuropathy
Severe combined immunodeficiency disease (Terrier type)
Severe combined immunodeficiency disease (Wetterhoun type)
Severe combined immunodeficiency disease, X-linked (Basset Hound type)
Severe combined immunodeficiency disease, X-linked (Corgi type)
Skeletal dysplasia 2
Spinal dysraphism (Weimaraner type)
Spinocerebellar ataxia
Startle disease
Thrombopathia (American Eskimo Dog type)
Thrombopathia (Basset Hound type)
Thrombopathia (Newfoundland type)
Trapped neutrophil syndrome
Vitamin D dependent rickets, type II
Von Willebrand disease I
Von Willebrand disease II
Testing performed prior to receiving his parents' results: