Pandora’s Cinnamon
Pandora’s Cinnamon Sire: Paco European Import Dam: Pandora’s Obsession European Import
Pandora’s Panda vom Boki’s Hause
Panda Pandora’s Panda vom Boki’s Hause Born: 20 May 2023KSS# JR 714957 FbAKC# DNA: V10103771 +h**Panda has been cleared through her DNA for more than 200 genetic diseases. A more comprehensive analysis is included at the bottom of her page. Panda is our newest European Import and we are so pleased with her! We have wanted to add a Fluffy female for a long time but waited until we found the perfect one! She is social, exudes sunshine and cannot get enough loves! Panda will be bred to a fluffy male and should have ALL FLUFFY PUPS summer 2025! Acral Mutilation Syndrome: WT/WT (clear)Acute Respiratory Distress Syndrome: WT/WT (clear)Adult Paroxysmal Dyskinesia: WT/WT (clear)Afibrinogenemia: WT/WT (clear)Alaskan Husky Encephalopathy: WT/WT (clear)Alaskan Malamute Polyneuropathy : WT/WT (clear)Amelogenesis Imperfecta: WT/WT (clear)Ataxia: WT/WT (clear)Benign Familial Juvenile Epilepsy: WT/WT (clear)Benard-Soulier Syndrome: WT/WT (clear)Canine Multiple System Degeneration: WT/WT (clear)Canine Scott Syndrome: WT/WT (clear)Cardiomyopathy and Juvenile Mortality: WT/WT (clear)Catalase Deficiency: WT/WT (clear)Centronuclear Myopathy: WT/WT (clear)Cerebellar Ataxia: WT/WT (clear)Cerebellar Ataxia 1 : WT/WT (clear)Cerebellar Ataxia 2 : WT/WT (clear)Cerebellar Cortical Degeneration: WT/WT (clear)Cerebellar Degeneration: WT/WT (clear)Charcot-Marie-Tooth Disease: WT/WT (clear)Chondrodysplasia: WT/WT (clear)Cleft Palate and Syndactyly: WT/WT (clear)Coagulation Factor VII Deficiency: WT/WT (clear)Collie Eye Anomaly: WT/WT (clear)Complement 3 Deficiency: WT/WT (clear)Cone Degeneration: WT/WT (clear)Congenital Hypothyroidism with Goiter: WT/WT (clear)Congenital Macrothrombocytopenia: WT/WT (clear)Congenital Methemoglobinemia: WT/WT (clear)Congenital Myasthenic Syndrome: WT/WT (clear)Congenital Stationary Night Blindness: WT/WT (clear)Copper Storage Disease: WT/WT (clear)Craniomandibular Osteopathy: WT/WT (clear)Cyclic Neutropenia: WT/WT (clear)Cystinuria: WT/WT (clear)Cystinuria Type 3 (Bulldog Type Risk Factor, Variant 3): WT/WT (clear)Cystinuria Type 3 (Bulldog Type Risk Factor, Variants 1 and 2): 1 copy carrierDandy-Walker-Like Malformation: WT/WT (clear)Darier Disease and Associated Infundibular Cyst Formation: WT/WT (clear)Deafness and Vestibular Dysfunction: WT/WT (clear)Degenerative Myelopathy WT/WT (clear)Degenerative Myelopathy Early-Onset Risk Modifier: WT/WT (clear)Dental Hypomineralization: WT/WT (clear)Diffuse Cystic Renal Dysplasia and Hepatic Fibrosis: WT/WT (clear)Dilated Cardiomyopathy: WT/WT (clear)Dry Eye Curly Coat Syndrome: WT/WT (clear)Dystrophic Epidermolysis Bullosa: WT/WT (clear)Early Onset Adult Deafness: WT/WT (clear)Early Retinal Degeneration: WT/WT (clear)Early-Onset Epilepsy: WT/WT (clear)Ectodermal Dysplasia: WT/WT (clear)Ectodermal Dysplasia, X-Linked: WT/WT (clear)Ehlers-Danlos Syndrome: WT/WT (clear)Elliptocytosis: WT/WT (clear)Epidermolytic Hyperkeratosis: WT/WT (clear)Episodic Falling Syndrome: WT/WT (clear)Exercise-Induced Collapse: WT/WT (clear)Exfoliative Cutaneous Lupus Erythematosus (ECLE): WT/WT (clear)Factor XI Deficiency: WT/WT (clear)Familial Nephropathy: WT/WT (clear)Fucosidosis: WT/WT (clear)Gallbladder Mucoceles: WT/WT (clear)Glanzmann’s Thrombasthenia: WT/WT (clear)Glaucoma: WT/WT (clear)Globoid Cell Leukodystrophy: WT/WT (clear)Glycogen Storage Disease Ia: WT/WT (clear)Glycogen Storage Disease IIIa: WT/WT (clear)Glycogen Storage Disease VII: WT/WT (clear)Glycogen Storage Disease VII, PFK Deficiency: WT/WT (clear)GM1 Gangliosidosis: WT/WT (clear)GM2 Gangliosidosis: WT/WT (clear)Greyhound Polyneuropathy: WT/WT (clear)Hemophilia A: WT/WT (clear)Hemophilia B: WT/WT (clear)Hereditary Ataxia: WT/WT (clear)Hereditary Cataracts: WT/WT (clear)Hereditary Footpad Hyperkeratosis: WT/WT (clear)Hereditary Nasal Parakeratosis: WT/WT (clear)Hereditary Nephritis: WT/WT (clear)Hyperuricosuria: WT/WT (clear)Hypomyelination: WT/WT (clear)Ichthyosis: WT/WT (clear)Inflammatory Myopathy: WT/WT (clear)Intervertebral Disc Disease Risk Factor and Chondrodystrophy (CDDY with IVDD): WT/WT (clear)Intestinal Cobalamin Malabsorption: WT/WT (clear)Intestinal Lipid Malabsorption: WT/WT (clear)Junctional Epidermolysis Bullosa: WT/WT (clear)Juvenile Laryngeal Paralysis and Polyneuropathy (JLPP): WT/WT (clear)Juvenile Myoclonic Epilepsy: WT/WT (clear)L-2-Hydroxyglutaric Aciduria: WT/WT (clear)Lagotto Storage Disease: WT/WT (clear)Laryngeal Paralysis and Polyneuropathy: WT/WT (clear)Late Onset Ataxia: WT/WT (clear)Lethal Acrodermatitis: WT/WT (clear)Leukocyte Adhesion Deficiency, Type I: WT/WT (clear)Leukocyte Adhesion Deficiency, Type III: WT/WT (clear)Ligneous Membranitis: WT/WT (clear)Limb-Girdle Muscular Dystrophy: WT/WT (clear)Lundehund Syndrome: WT/WT (clear)Macular Corneal Dystrophy: WT/WT (clear)Mammary Tumors: WT/WT (clear)May-Hegglin Anomaly: WT/WT (clear)Microphthalmia: WT/WT (clear)Mucopolysaccharidosis I: WT/WT (clear)Mucopolysaccharidosis IIIA: WT/WT (clear)Mucopolysaccharidosis IIIB: WT/WT (clear)Mucopolysaccharidosis VI: WT/WT (clear)Mucopolysaccharidosis VII: WT/WT (clear)Multidrug Resistance 1: WT/WT (clear)Multifocal Retinopathy1: WT/WT (clear)Multifocal Retinopathy 2: WT/WT (clear)Multifocal Retinopathy 3: WT/WT (clear)Muscular Dystrophy: WT/WT (clear)Musladin-Lueke Syndrome: WT/WT (clear)Myostatin Deficiency: WT/WT (clear)Mytonia Congenita: WT/WT (clear)Myotubular Myopathy 1: WT/WT (clear)Narcolepsy: WT/WT (clear)Neonatal Ataxia: WT/WT (clear)Neonatal Cerebellar Cortical Degeneration: WT/WT (clear)Neonatal Encephalopathy with Seizures: WT/WT (clear)Neuroaxonal Dystrophy: WT/WT (clear)Neuronal Ceroid Lipofuscinosis 1: WT/WT (clear)Neuronal Ceroid Lipofuscinosis 10: WT/WT (clear)Neuronal Ceroid Lipofuscinosis 12: WT/WT (clear)Neuronal Ceroid Lipofuscinosis 2: WT/WT (clear)Neuronal Ceroid Lipofuscinosis 4A: WT/WT (clear)Neuronal Ceroid Lipofuscinosis 5: WT/WT (clear)Neuronal Ceroid Lipofuscinosis 6: WT/WT (clear)Neuronal Ceroid Lipofuscinosis 7: WT/WT (clear)Neuronal Ceroid Lipofuscinosis 8: WT/WT (clear)Nonsyndromic Hearing Loss: WT/WT (clear)Oculocutaneous Albinism: WT/WT (clear)Osteochondrodysplasia: WT/WT (clear)Osteogenesis Imperfecta: WT/WT (clear)P2RY12 Receptor Platelet Disorder: WT/WT (clear)Pancreatitis: WT/WT (clear)Pembroke Welsh Corgi Duchenne Muscular Dystrophy: WT/WT (clear)Persistent Mullerian Duct Syndrome: WT/WT (clear)Pituitary Dwarfism: WT/WT (clear)Polyneuropathy: WT/WT (clear)Polyneuropathy with Ocular Abnormalities and Neuronal Vacuolation: WT/WT (clear)Pompe Disease: WT/WT (clear)Prekallikrein Deficiency: WT/WT (clear)Primary Ciliary Dyskinesia: WT/WT (clear)Primary Hyperoxaluria: WT/WT (clear)Primary Lens Luxation: WT/WT (clear)Primary Open Angle Glaucoma: WT/WT (clear)Primary Open Angle Glaucoma and Primary Lens Luxation: WT/WT (clear)Progressive Retinal Atrophy: WT/WT (clear)Progressive Retinal Atrophy, Cone-Rod Dystrophy: WT/WT (clear)Progressive Retinal Atrophy, Cone-Rod Dystrophy 1: WT/WT (clear)Progressive Retinal Atrophy, Cone-Rod Dystrophy 2: WT/WT (clear)Progressive Retinal Atrophy, Cone-Rod Dystrophy 3: WT/WT (clear)Progressive Retinal Atrophy, Cone-Rod Dystrophy 4: WT/WT (clear)Progressive Retinal Atrophy, Early Onset: WT/WT (clear)Progressive Retinal Atrophy, Generalized: WT/WT (clear)Progressive Retinal Atrophy, Late-Onset: WT/WT (clear)Progressive Retinal Atrophy, PRA1: WT/WT (clear)Progressive Retinal Atrophy, PRA3: WT/WT (clear)Progressive Retinal Atrophy, Progressive Cone-Rod Degeneration (prcd): WT/WT (clear)Progressive Retinal Atrophy, Cone-Rod Dysplasia 3: WT/WT (clear)Progressive Retinal Atrophy, Cone-Rod Dysplasia 4: WT/WT (clear)Progressive Retinal Atrophy, Syndromic Retinal Degeneration: WT/WT (clear)Progressive Retinal Atrophy, X-Linked 1: WT/WT (clear)Progressive Retinal Atrophy, X-Linked 2: WT/WT (clear)Protein Losing Nephropathy: WT/WT (clear)Pyruvate Dehydrogenase Deficiency: WT/WT (clear)Pyruvate Kinase Deficiency: WT/WT (clear)Recurrent Inflammatory Pulmonary Disease: WT/WT (clear)Renal Cystadenocarcinoma and Nodular Dermatofibrosis: WT/WT (clear)Retinal Dysplasia/Oculoskeletal Dysplasia 1: WT/WT (clear)Dysplasia/Oculoskeletal Dysplasia 2: WT/WT (clear)Sensory Neuropathy: WT/WT (clear)Severe Combined Immunodeficiency Disease: WT/WT (clear)Severe Combined Immunodeficiency Disease, X-Linked: WT/WT (clear)Shar-Pei Autoinflammatory Disease: WT/WT (clear)Skeletal Dysplasia 2: WT/WT (clear)Spinal Dysraphism: WT/WT (clear)Spinocerebellar Ataxia: WT/WT (clear)Spondylocostal Dysostosis: WT/WT (clear)Stargardt Disease: WT/WT (clear)Startle Disease: WT/WT (clear)Subacute Necrotizing Encephalopathy: WT/WT (clear)Thrombopathia: WT/WT (clear)Trapped Neutrophil Syndrome: WT/WT (clear)Ullrich Congenital Muscular Dystrophy (LR Type 1): WT/WT (clear)Ullrich Congenital Muscular Dystrophy (LR Type 2): WT/WT (clear)Urolithiasis: WT/WT (clear)Van Den Ende-Gupta Syndrome: WT/WT (clear)Von Willebrand Disease 1: WT/WT (clear)Von Willebrand Disease II: WT/WT (clear)Von Willebrand Disease III: WT/WT (clear) Eyes:Hereditary Cataracts: WT/WT (clear)Hyperuricosuria: WT/WT (clear)Multifocal Retinopathy 1: WT/WT (clear)Oculocutaneous Albinism: WT/WT (clear)Progressive Retinal Atrophy, Cone-Rod Dystrophy 4: WT/WT (clear) Coat:A Locus: AyAt- (Sable/fawn; carries tricolor/black & tan)B Locos: B/b- (Black coat, nose, foot pads; carries 1 copy brown)Co Locos: CO/CO- Black coat, nose & foot pads (does not carry cocoa)Cu Locos: Cu/Cu- Straight coatD Locus: D/d- Carries one copy dilute colorE Locus: E/e- Carrier Melanistic Mask (face color), yellow/redL Locus: Sh/Sh- Does not carry FluffyM
Pandora’s Bleu
Pandora’s Bleu
Pandora’s Biskit
Pandora’s Biskit
Pandora’s Bella
Pandora’s Bella Pandora’s Bella is absolutely the Belle of the ball! Her name is Spanish for “beautiful” and very much suits her. She is an elegant lady that exudes sunshine and love. Bella has a compact frame with very harmonious anatomy. She has a beautiful blue and cream coat and the very pale shade of cream against the beautiful hue of blue is just mesmerizing. Bella loves any game that invites engaging and cannot get enough cuddles. Pandora’s Bella at 10 weeks!
Pandora’s Blossom
Pandora’s Blossom Blossom and her brother Biskit were our 2 tiny pups in this litter and will likely be teacup like their mama! But small in stature only as they both have SOO MUCH personality packed into their tiny frames. We call Blossom our little teacup pup and being the clever little girl that she is, she has already sorted out how adorable she is and completely uses that to her advantage. She is enthusiasm and happiness packed into this absolutely irresistible little package! Blossom is a very rare lilac color with beautiful fawn markings and those impossible to miss baby blue eyes. Pandora’s Blossom at 10 weeks old
Pandora’s Bianca
Pandora’s Bianca The ever so gorgeous Bianca at 2.5 months old <3 Bianca is a confident, curious little girl who is always up for an adventure. She loves her peoples and cannot get enough attention or affection. Bianca is blue and fawn with a very compact, stocky frame and beautiful assembly. She has great bone and substance and is going to be a very beautiful girl when grown. Beautiful miss Bianca at 3.5 months old <3
Pandora’s Bambi
Pandora’s Bambi Pandora’s Bambi is one of the most rare colors for this breed- Lilac <3 Bambi also has beautiful fawn markings that artfully decorate that pale lilac canvas. In addition to being a very rare color, Liliac pups are also unique in eye color! They will always have light eyes! Bambi has piercing blue eyes, that along with a very expressive face, just communicate with your soul <3 Bambi is a very gentle, loving, trusting pup who absolutely adores her peoples.
Pandora’s Acorn
Pandora’s Acorn
Pandora’s Atari
Pandora’s Atari