Also called: Neurodegenerative diseases
Important: This page is general information, not medical advice. It does not recommend or prescribe any treatment. Always consult your doctor or pharmacist before starting, stopping or changing any medicine.
About Degenerative Nerve Diseases
Degenerative nerve diseases affect many of your body's activities, such as balance, movement, talking, breathing, and heart function. Many of these diseases are genetic. Sometimes the cause is a medical condition such as alcoholism, a tumor, or a stroke. Other causes may include toxins, chemicals, and viruses. Sometimes the cause is unknown.
Degenerative nerve diseases include:
- Alzheimer's disease
- Amyotrophic lateral sclerosis
- Friedreich ataxia
- Huntington's disease
- Lewy body disease
- Parkinson's disease
- Spinal muscular atrophy
Degenerative nerve diseases can be serious or life-threatening. It depends on the type. Most of them have no cure. Treatments may help improve symptoms, relieve pain, and increase mobility.
It sits within Brain and Nerves.
The lead U.S. institute for this subject is the National Institute of Neurological Disorders and Stroke.
When to speak to someone. Reading about a topic cannot tell you whether it applies to you. Speak to a doctor or pharmacist if symptoms are severe, sudden, getting worse, or simply not going away — and seek emergency care immediately for chest pain, breathing difficulty, sudden weakness or confusion, or a serious allergic reaction.
Research on Degenerative Nerve Diseases
1,260 studies areregistered for this condition on ClinicalTrials.gov, the U.S. National Library of Medicine's public registry. A selection is below — the links go straight to the registry entry, not to a summary of ours.
What a registered study does and does not mean. Registration means a study exists and has been declared publicly. It says nothing about whether the treatment being tested works, is safe, or is available to you. Many studies find no benefit — that is what research is for. Never seek out an experimental treatment on the strength of a registry entry alone.
Research currently under way
- A Study of SGT-212 Gene Therapy in Friedreich's AtaxiaSolid Biosciences Inc.
- ARTFL LEFFTDS Longitudinal Frontotemporal Lobar Degeneration (ALLFTD)Mayo Clinic
- Developing a Comprehensive Biomarker Panel for Monitoring Progression and Early Detection in ALS PatientsUniversity Hospital, Montpellier
- Characterization of the Cardiac Phenotype of Friedreich's Ataxia (FRDA)Weill Medical College of Cornell University
- Moderate Versus High Volume Light-Moderate Intensity Exercise for People With Moderate Parkinson's DiseaseVA Office of Research and Development
- A Study to Evaluate the Efficacy of NIO752 in Participants With Progressive Supranuclear PalsyNovartis Pharmaceuticals
Research already completed
- Natural History and Biomarkers of Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Caused by the C9ORF72 Gene MutationNational Institute of Neurological Disorders and Stroke (NINDS)
- CADASIL Disease DiscoveryNational Heart, Lung, and Blood Institute (NHLBI)
Study data from ClinicalTrials.gov, a service of the U.S. National Library of Medicine. Retrieved 2026-07-30. Registry entries are supplied by study sponsors and investigators; ClinicalTrials.gov does not verify their scientific validity. PocketsInfo is not affiliated with, and not endorsed by, the NLM or the NIH.
Where to read more
Rather than paraphrase, we point you to the primary sources. Every link below is to a government health agency, a national institute or a recognised medical body — grouped by what you are trying to find out.
Diagnosis and Tests
- Electromyography (EMG) and Nerve Conduction StudiesNational Library of Medicine
Genetics
- Alpers-Huttenlocher syndrome: MedlinePlus GeneticsNational Library of Medicine
- Alpha-methylacyl-CoA racemase deficiency: MedlinePlus GeneticsNational Library of Medicine
- Andermann syndrome: MedlinePlus GeneticsNational Library of Medicine
- Ataxia neuropathy spectrum: MedlinePlus GeneticsNational Library of Medicine
- Autosomal dominant cerebellar ataxia, deafness, and narcolepsy: MedlinePlus GeneticsNational Library of Medicine
- CLN1 disease: MedlinePlus GeneticsNational Library of Medicine
- CLN10 disease: MedlinePlus GeneticsNational Library of Medicine
- CLN2 disease: MedlinePlus GeneticsNational Library of Medicine
- CLN3 disease: MedlinePlus GeneticsNational Library of Medicine
- CLN5 disease: MedlinePlus GeneticsNational Library of Medicine
- CLN6 disease: MedlinePlus GeneticsNational Library of Medicine
- CLN7 disease: MedlinePlus GeneticsNational Library of Medicine
- CLN8 disease: MedlinePlus GeneticsNational Library of Medicine
- Congenital insensitivity to pain with anhidrosis: MedlinePlus GeneticsNational Library of Medicine
- Familial encephalopathy with neuroserpin inclusion bodies: MedlinePlus GeneticsNational Library of Medicine
- Fatty acid hydroxylase-associated neurodegeneration: MedlinePlus GeneticsNational Library of Medicine
- GM2 activator deficiency: MedlinePlus GeneticsNational Library of Medicine
- Hereditary sensory and autonomic neuropathy type IE: MedlinePlus GeneticsNational Library of Medicine
- Hereditary sensory and autonomic neuropathy type II: MedlinePlus GeneticsNational Library of Medicine
- Hereditary sensory and autonomic neuropathy type V: MedlinePlus GeneticsNational Library of Medicine
- Infantile-onset ascending hereditary spastic paralysis: MedlinePlus GeneticsNational Library of Medicine
Clinical Trials
- ClinicalTrials.gov: Neurodegenerative DiseasesNational Institutes of Health
- ClinicalTrials.gov: Prion DiseasesNational Institutes of Health
Medical subject headings
Clinicians and researchers index this subject under Neurodegenerative Diseases. These are the terms to use when searching medical literature.
This page is built from the MedlinePlus health topic record for Degenerative Nerve Diseases, a service of the U.S. National Library of Medicine (NLM), National Institutes of Health. Information is from MedlinePlus.gov. PocketsInfo is not affiliated with, and is not endorsed by, the NLM or the NIH. Retrieved 30 July 2026.