Neurology | Human Genetic Diagnostics
Many health disorders or development peculiarities are subject to hereditary influences. Especially rare syndroms often have genetic reasons. This also applies neurological diseases like Epilepsy, Morbus Parkinson, Dementia or Autism. We are happy to advise your patients if the diagnosed disease possibly has genetic reasons and explain possible effects to the patient himself or his relatives.
Neurology (Panel testing)
Epilepsie
- Absence - Epilepsy
- Angelman / Angelmanlike Syndrome
- Benigne Neonatal cramps
- Dravet-Syndrome
- Epilepsy with elevated need for therapy
- Epileptic Enzephalopathie
- Family hemiplegic migraine
- Family nocturnal Frontal Lobe Epilepsy (ADNFLE)
- Focal Epilepsy
- Early Childhood epileptic Enzephalopathy
- Generalised Epilepsy with febrile seizures (GEFS)
- Generalised, juvenile, myoklonic Epilepsy
- Hereditary Hyperekplexy
- Creatine deficiency syndrome
- Landau-Kleffner-Syndrome
- Lennox-Gastaut-Syndrome
- Ohtahara-Syndrome
- Progressive myoclonic Epilepsy
- Rett Syndrome and Rett similar disorders
- West-Syndrome (Epileptic Encephalopathy Typ 1)
Neuromuscular diseases
- Hereditary Neuropathie
- Myasthene-Syndrome
- Myopathies
- Myotonies
- Periodic Paralyses
- Spinal Muscelatrophy
Neurodegenerative diseases
- Alzheimer disease
- Ataxia und differential diagnosis
- Basal ganglia calcification
- Cerebral Microangiopathy
- Dystonia
- Hereditary Spastic Spinal paralysis (HSP)
- Leukodystrophy/ Leukencephalopathy
- Parkinson Disease