Hereditary Diseases Cat

Diagnostic spectrum

• Genetic blood group determination
• Alpha-Mannosidosis (AMD)
• Autoimmune lymphoproliferative Syndrome (ALPS)
• Congenital myasthenic syndrome (CMS)
• Cystinuria (CysK)
• Gangliosidosis (GM 1/GM 2)
• Gangliosidosis (GM2)
• Glycogen storage disease type IV (GSD4)
• Head Defect
• Hypertrophic cardiomyopathy (HCM1)
• Hypertrophic cardiomyopathy (HCM3)
• Hypokalemia
• Hypotrichosis and short life expectancy
• Mucopolysaccharidosis type VI (MPS6)
• Mucopolysaccharidosis type VII (MPS7)
• Myotonia congenita
• Osteochondrodysplasia (OCD)
• Polycystic kidney disease (PKD)
• Primary congenital glaucoma (PCG)
• Progressive retinal atrophy (b-PRA)*
• Progressive retinal atrophy (pd-PRA)
• Progressive retinal atrophy (rdAc-PRA)
• Progressive retinal atrophy (rdy-PRA)
• Pyruvate kinase deficiency (PK)
• Serological Blood Group Typing
• Spinal muscular atrophy (SMA)