Neurogenetics

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.

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