Hereditary Diseases Horse

Diagnostic spectrum

• Androgen insensitivity syndrome (AIS)
• Cerebellar abiotrophy (CA)
• Equine malignant hyperthermia (EMH)
• Hereditary myotonia
• Foal immunodeficiency syndrome (FIS)
• Glycogen branching enzyme deficiency (GBED)
• Hereditary equine regional dermal asthenia (HERDA)
• Hereditary junctional epidermolysis bullosa (JEB)
• Hoof wall separation disease (HWSD)
• Hydrocephalus
• Hyperkalemic periodic paralysis (HYPP)
• Idiopathic hypocalcaemia
• Immune mediated myositis & MYH1 Myopathy (MYHM)
• Lavender foal syndrome (LFS)
• Naked foal syndrome (NFS)
• Ocular squamous cell carcinoma (SCC)
• Polysaccharid storage myopathy type 1 (PSSM)
• Severe combined immuno deficiency (SCID)
• Lethal white foal syndrome (LWO)
• Warmblood fragile foal syndrome (WFFS)
• Dwarfism
• Dwarfism (ACAN)