Asper Neurogenetics

Amyotrophic Lateral Sclerosis
Autism Spectrum Disorders
Brunner Syndrome
Charcot-Marie-Tooth Disease 
Congenital Muscular Dystrophy
Congenital Myasthenic Syndrome
Congenital Myopathy and Distal Myopathy
Familial Hemiplegic Migraine
Fragile X Syndrome
Frontotemporal Dementia
Hereditary Ataxia
Hereditary Spastic Paraplegia 
Leukodystrophy and Leukoencephalopathy 
Limb-Girdle Muscular Dystrophy
Malignant Hyperthermia
Menkes Disease
Metabolic Myopathy and Rhabdomyolysis UPDATED
Mitochondrial Diseases
Myotonia Congenita NEW
Myotonic Dystrophy type I 
Myotonic Dystrophy type II 
Neurodegeneration with Brain Iron Accumulation
Oculopharyngeal Muscular Dystrophy 
Parkinson’s Disease
Paroxysmal Dyskinesia
Smith-Lemli-Opitz Syndrome
Spinocerebellar ataxia type 12
Tuberous Sclerosis
Unverricht Lundborg diseases 
Wilson Disease
Whole Exome Sequencing

Asper Neurogenetics includes genetic tests for the diagnostics of diseases with neurologic and metabolic involvement.

Diseases involved in the testing portfolio are genetically and phenotypically heterogeneous group of severe disorders such as inherited neuropathies and mitochondrial diseases. For the diagnostics of diseases with an overlapping spectrum of phenotypes, we offer a comprehensive variety of tests with different testing strategies.