Upstate New York, United States
Health Guarantee
6 Year Health Guarantee
We offer a 6 year health guarantee, most breeders offer the state minimums, we at Brooklea Beauties offer a lengthy guarantee because we have the utmost faith in our breeding stock. We offer this health guarantee because the health of all of our dogs genetically has been extremely sound.
Warranty -
Warranty:
The Puppy/Dog is sold to Buyer and Buyer purchases and accepts the Puppy/Dog in “as is” condition and Breeder makes no guarantees or warranties, express or implied concerning the Puppy (Dog) (Dog)’s health provided, however that:
i. Breeder guarantees that for period of (6) years from the date of birth of the Puppy/Dog, the Puppy/Dog will not have nor develop the following conditions: Genetically caused Congenital Hip or Elbow Dysplasia, PRA, Von willebrands Disease, Ichthyosis, Degenerative Myelopathy, GR-PRA-2, Progressive Retinal Atrophy, Progressive Rod-Cone Degeneration, GR-PRA1, Neuronal Ceroid Lipofuscinosis, Muscular Dystrophy, Dystrophic Epidermolysis Bullosa, Osteogenesis Imperfecta, GM2 Gangliosidosis, Chondrodystrophy and Intervertebral Disc Disease, Congenital Macrothrombocytopenia, Osteochondrodysplasia.
ii. If Buyers Licensed Veterinarian provides a written opinion including diagnostic proof that Puppy/Dog has one of the above listed conditions and that it is genetically caused and such a claim is made up to 72 months (6 YR) from Puppy/Dog’s date of birth the Breeder shall have an obligation to provide monetary reimbursement of up to the price of canine as follows: up to 24 months of Puppy/Dog’s age a full refund of purchase price for Puppy/Dog, 24-48 months of dog’s life ¾ purchase price, 48-72 months of dog’s life ½ the purchase price. Please note any sales tax collected on sale price will not be refundable.
iii. The above listed diagnosis must be confirmed and mailed from a licensed Veterinarian/Specialist’s practice to the Breeder and surgery/correction must be completed prior to reimbursement; proof of payment to specialist for surgery must be provided to Breeder prior to compensation for surgery. Any notation of ailment prior to 6 years of age will qualify for a later surgery if Veterinary Specialist has sent written proof to Breeder that the condition is genetically caused but does not require surgery at the time of diagnosis.
iv. This guarantee is not transferable.
What Health Testing we do here:
ALL OF OUR DOGS ARE TESTED FOR ALL OF THE BELOW PLUS MORE
We test for over 160 known genetic health conditions in 16 different areas, per displayed below:
Clinical
MDR1 Drug Sensitivity (MDR1)Alanine Aminotransferase Activity (GPT)
Blood
P2Y12 Receptor Platelet Disorder (P2RY12)Factor IX Deficiency, Hemophilia B (F9 Exon 7, Terrier Variant)Factor IX Deficiency, Hemophilia B (F9 Exon 7, Rhodesian Ridgeback Variant)Factor VII Deficiency (F7 Exon 5)Factor VIII Deficiency, Hemophilia A (F8 Exon 10, Boxer Variant)Factor VIII Deficiency, Hemophilia A (F8 Exon 11, Shepherd Variant 1)Factor VIII Deficiency, Hemophilia A (F8 Exon 1, Shepherd Variant 2)Thrombopathia (RASGRP2 Exon 5, Basset Hound Variant)Thrombopathia (RASGRP2 Exon 8)Thrombopathia (RASGRP2 Exon 5, American Eskimo Dog Variant)Von Willebrand Disease Type II (VWF Exon 28)Von Willebrand Disease Type III (VWF Exon 4)Von Willebrand Disease Type I (VWF)Canine Leukocyte Adhesion Deficiency Type III (LAD3) (FERMT3)Congenital Macrothrombocytopenia (TUBB1 Exon 1, Cavalier King Charles Spaniel Variant)Canine Elliptocytosis (SPTB Exon 30)Cyclic Neutropenia, Gray Collie Syndrome (AP3B1 Exon 20)Glanzmann's Thrombasthenia Type I (ITGA2B Exon 12)May-Hegglin Anomaly (MYH9)Prekallikrein Deficiency (KLKB1 Exon 8)Pyruvate Kinase Deficiency (PKLR Exon 5)Pyruvate Kinase Deficiency (PKLR Exon 7 Labrador Variant)Pyruvate Kinase Deficiency (PKLR Exon 7 Pug Variant)Pyruvate Kinase Deficiency (PKLR Exon 7 Beagle Variant)Pyruvate Kinase Deficiency (PKLR Exon 10)Trapped Neutrophil Syndrome (VPS13B)Ligneous Membranitis (PLG)
Immune
Complement 3 (C3) deficiency (C3)Severe Combined Immunodeficiency (PRKDC)Severe Combined Immunodeficiency (RAG1)X-linked Severe Combined Immunodeficiency(IL2RG Variant 1)X-linked Severe Combined Immunodeficiency(IL2RG Variant 2)
Hormones
Congenital Hypothyroidism (TPO, Tenterfield Terrier Variant)
Eyes
Progressive Retinal Atrophy - rcd1 Rod-cone dysplasia, rcd1 (PDE6B Exon 21 Irish Setter Variant)Progressive Retinal Atrophy Rod-cone dysplasia, rcd1a (PDE6B Exon 21 Sloughi Variant)Progressive Retinal Atrophy - rcd3 Rod-cone dysplasia, rcd3 (PDE6A)Progressive Retinal Atrophy - CNGA (CNGA1 Exon 9)Progressive Retinal Atrophy - prcd Progressive rod-cone degeneration (PRCD Exon 1)Progressive Retinal Atrophy (CNGB1)Progressive Retinal Atrophy (SAG)Golden Retriever Progressive Retinal Atrophy 1(SLC4A3)Golden Retriever Progressive Retinal Atrophy 2(TTC8)Progressive Retinal Atrophy - crd1 (PDE6B)Progressive Retinal Atrophy - crd2 (IQCB1)Progressive Retinal Atrophy - crd4/cord1(RPGRIP1)Collie Eye Anomaly, Choroidal Hypoplasia (NHEJ1)Achromatopsia (CNGA3 Exon 7 German Shepherd Variant)Achromatopsia (CNGA3 Exon 7 Labrador Retriever Variant)Autosomal Dominant Progressive Retinal Atrophy(RHO)Canine Multifocal Retinopathy cmr1 (BEST1 Exon 2)Canine Multifocal Retinopathy cmr2 (BEST1 Exon 5)Canine Multifocal Retinopathy cmr3 (BEST1 Exon 10 Deletion)Canine Multifocal Retinopathy cmr3 (BEST1 Exon 10 SNP)Glaucoma Primary Open Angle Glaucoma (ADAMTS10 Exon 9)Glaucoma Primary Open Angle Glaucoma (ADAMTS10 Exon 17)Glaucoma Primary Open Angle Glaucoma (ADAMTS17 Exon 11)Glaucoma Primary Open Angle Glaucoma (ADAMTS17 Exon 2)Hereditary Cataracts, Early-Onset Cataracts, Juvenile Cataracts (HSF4 Exon 9 Shepherd Variant)Primary Lens Luxation (ADAMTS17)Congenital stationary night blindness (RPE65)Macular Corneal Dystrophy (MCD) (CHST6)
Multisystem
Glycogen Storage Disease Type Ia, Von Gierke Disease (G6PC)Primary Ciliary Dyskinesia (CCDC39 Exon 3)Congenital Keratoconjunctivitis Sicca and Ichthyosiform Dermatosis (CKCSID), Dry Eye Curly Coat Syndrome (FAM83H Exon 5)X-linked Ectodermal Dysplasia, Anhidrotic Ectodermal Dysplasia (EDA Intron 8)Renal Cystadenocarcinoma and Nodular Dermatofibrosis (RCND) (FLCN Exon 7)Canine Fucosidosis (FUCA1)Glycogen Storage Disease Type II, Pompe's Disease (GAA)Glycogen Storage Disease Type IIIa (GSD IIIa)(AGL)Mucopolysaccharidosis Type I (IDUA)Mucopolysaccharidosis Type IIIA, Sanfilippo Syndrome Type A (SGSH Exon 6 Variant 1)Mucopolysaccharidosis Type IIIA, Sanfilippo Syndrome Type A (SGSH Exon 6 Variant 2)Mucopolysaccharidosis Type VII, Sly Syndrome(GUSB Exon 5)Mucopolysaccharidosis Type VII, Sly Syndrome(GUSB Exon 3)Glycogen storage disease Type VII, Phosphofructokinase deficiency (PFKM Whippet and English Springer Spaniel Variant)Glycogen storage disease Type VII, Phosphofructokinase deficiency (PFKM Wachtelhund Variant)Lagotto Storage Disease (ATG4D)Neuronal Ceroid Lipofuscinosis 1 (PPT1 Exon 8)Neuronal Ceroid Lipofuscinosis 2 (TPP1 Exon 4)Neuronal Ceroid Lipofuscinosis 1, Cerebellar Ataxia - NCL-A (ARSG Exon 2)Neuronal Ceroid Lipofuscinosis 1 (CLN5 Border Collie Variant)Neuronal Ceroid Lipofuscinosis 6 (CLN6 Exon 7)Neuronal Ceroid Lipofuscinosis 8 (CLN8 Exon 2)Neuronal Ceroid Lipofuscinosis (MFSD8)Neuronal Ceroid Lipofuscinosis (CLN8)Neuronal Ceroid Lipofuscinosis 10 (CTSD Exon 5)Neuronal Ceroid Lipofuscinosis (CLN5 Golden Retriever Variant)Adult-Onset Neuronal Ceroid Lipofuscinosis(ATP13A2)GM1 Gangliosidosis (GLB1 Exon 15 Shiba Inu Variant)GM1 Gangliosidosis (GLB1 Exon 15 Alaskan Husky Variant)GM1 Gangliosidosis (GLB1 Exon 2)GM2 Gangliosidosis (HEXB, Poodle Variant)GM2 Gangliosidosis (HEXA)Globoid Cell Leukodystrophy, Krabbe disease(GALC Exon 5)
Kidney and Bladder
2,8-Dihydroxyadenine (2,8-DHA) Urolithiasis(APRT)Cystinuria Type I-A (SLC3A1)Cystinuria Type II-A (SLC3A1)Cystinuria Type I-A (SLC7A9)Hyperuricosuria and Hyperuricemia or Urolithiasis(SLC2A9)Polycystic Kidney Disease (PKD1)Primary Hyperoxaluria (AGXT)Protein Losing Nephropathy (NPHS1)X-Linked Hereditary Nephropathy (Samoyed Variant 2) (COL4A5 Exon 35)Autosomal Recessive Hereditary Nephropathy, Familial Nephropathy (COL4A4 Exon 3)
Other Systems
Autosomal Recessive Amelogenesis Imperfecta(Italian Greyhound Variant)Persistent Mullerian Duct Syndrome (AMHR2)Deafness and Vestibular Syndrome of Dobermans (DVDob, DINGS)Shar-Pei Autoinflammatory Disease (SPAID, Shar-Pei Fever) (MTBP)
Brain and Spinal Cord
Alaskan Husky Encephalopathy, Subacute Necrotizing Encephalomyelopathy (SLC19A3)Alexander Disease (GFAP)Cerebellar Abiotrophy, Neonatal Cerebellar Cortical Degeneration (SPTBN2)Cerebellar Ataxia, Progressive Early-Onset Cerebellar Ataxia (SEL1L)Cerebellar Hypoplasia (VLDLR)Spinocerebellar Ataxia, Late-Onset Ataxia(CAPN1)Spinocerebellar Ataxia with Myokymia and/or Seizures (KCNJ10)Benign Familial Juvenile Epilepsy, Remitting Focal Epilepsy (LGI2)Degenerative Myelopathy (SOD1A)Fetal-Onset Neonatal Neuroaxonal Dystrophy(MFN2)Hypomyelination and Tremors (FNIP2)Shaking Puppy Syndrome, X-linked Generalized Tremor Syndrome (PLP)L-2-Hydroxyglutaricaciduria (L2HGDH)Neonatal Encephalopathy with Seizures (NEWS)(ATF2)Polyneuropathy, NDRG1 Greyhound Variant(NDRG1 Exon 15)Polyneuropathy, NDRG1 Malamute Variant (NDRG1 Exon 4)Narcolepsy (HCRTR2 Intron 6)Progressive Neuronal Abiotrophy (Canine Multiple System Degeneration) (SERAC1 Exon 15)Progressive Neuronal Abiotrophy (Canine Multiple System Degeneration) (SERAC1 Exon 4)Juvenile Laryngeal Paralysis and Polyneuropathy(RAB3GAP1)Hereditary Sensory Autonomic Neuropathy (HSAN), Acral Mutilation Syndrome (GDNF-AS)Juvenile-Onset Polyneuropathy, Leonberger Polyneuropathy 1 (LPN1, ARHGEF10)Spongy Degeneration with Cerebellar Ataxia 1 (SDCA1), SeSAME/EAST (KCNJ10)Spongy Degeneration with Cerebellar Ataxia 2 (SDCA2) (ATP1B2)
Heart
Dilated Cardiomyopathy (PDK4)Long QT Syndrome (KCNQ1)
Muscular
Muscular Dystrophy Cavalier King Charles Spaniel Variant 1Muscular Dystrophy Muscular Dystrophy (DMD Pembroke Welsh Corgi Variant )Muscular Dystrophy Muscular Dystrophy (DMD Golden Retriever Variant)Centronuclear Myopathy (PTPLA)Exercise-Induced Collapse (DNM1)Inherited Myopathy of Great Danes (BIN1)Myostatin Deficiency, Bully Whippet Syndrome(MSTN)Myotonia Congenita (CLCN1 Exon 7)Myotonia Congenita (CLCN1 Exon 23)Myotubular Myopathy 1, X-linked Myotubular Myopathy (MTM1)
Metabolic
Hypocatalasia, Acatalasemia (CAT)Pyruvate Dehydrogenase Deficiency (PDP1)Malignant Hyperthermia (RYR1)
Gastro-intestinal
Imerslund-Grasbeck Syndrome, Selective Cobalamin Malabsorption (CUBN Exon 53)Imerslund-Grasbeck Syndrome, Selective Cobalamin Malabsorption (CUBN Exon 8)
Neuro-muscular
Congenital Myasthenic Syndrome (CHAT)Congenital Myasthenic Syndrome (COLQ)Episodic Falling Syndrome (BCAN)
Skin & Connective Tissues
Dystrophic Epidermolysis Bullosa (COL7A1)Ectodermal Dysplasia, Skin Fragility Syndrome(PKP1)Ichthyosis, Epidermolytic Hyperkeratosis (KRT10)Ichthyosis (PNPLA1)Ichthyosis (SLC27A4)Ichthyosis (NIPAL4)Focal Non-Epidermolytic Palmoplantar Keratoderma, Pachyonychia Congenita (KRT16)Hereditary Footpad Hyperkeratosis (FAM83G)Hereditary Nasal Parakeratosis (SUV39H2)Musladin-Lueke Syndrome (ADAMTSL2)
Skeletal
Cleft Lip and/or Cleft Palate (ADAMTS20)Hereditary Vitamin D-Resistant Rickets (VDR)Oculoskeletal Dysplasia 1, Dwarfism-Retinal Dysplasia (COL9A3, Labrador Retriever)Osteogenesis Imperfecta, Brittle Bone Disease(COL1A2)Osteogenesis Imperfecta, Brittle Bone Disease(SERPINH1)Osteogenesis Imperfecta, Brittle Bone Disease(COL1A1)Osteochondrodysplasia, Skeletal Dwarfism(SLC13A1)Skeletal Dysplasia 2 (COL11A2)Craniomandibular Osteopathy (CMO) (SLC37A2)
HIPS, ELBOWS, THYROID, PATELLA all completed by OFA, PENNHIP or other recognized veterinary testing practices.
New Applicants Welcome
Now Accepting applications for Summer & Fall 2023, Limited spaces available Get your application in Today!