Asper Neurogenetics

Amyotrophic Lateral Sclerosis
Autism Spectrum Disorders UPDATED
Brunner Syndrome
Charcot-Marie-Tooth Disease UPDATED
Congenital Muscular Dystrophy NEW
Congenital Myasthenic Syndrome
Congenital Myopathy and Distal Myopathy
Cornelia de Lange Syndrome UPDATED
Craniosynostosis
Dystonia UPDATED
Epilepsy UPDATED
Familial Hemiplegic Migraine NEW
Fragile X Syndrome
Frontotemporal Dementia
Hereditary Ataxia UPDATED
Hereditary Spastic Paraplegia UPDATED
Joubert Syndrome
Leukodystrophy and Leukoencephalopathy
Limb-Girdle Muscular Dystrophy UPDATED
Malignant Hyperthermia UPDATED
Menkes Disease
Microcephaly UPDATED
Mitochondrial Diseases UPDATED
Neurodegeneration with Brain Iron Accumulation
Parkinson’s Disease
Paroxysmal Dyskinesia NEW
Smith-Lemli-Opitz Syndrome
Tuberous Sclerosis
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.