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

Whole Genom Sequencing

​

Genetic Passport 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.