Acute motor and sensory axonal neuropathy
An axonal variant of Guillain-Barré syndrome affecting motor and sensory nerves.
An alphabetical guide to conditions mentioned on FND Nope. Browse a subject and follow the related posts.
98 conditions
An axonal variant of Guillain-Barré syndrome affecting motor and sensory nerves.
A progressive motor neuron disease causing weakness and muscle wasting.
A neurological syndrome involving impaired coordination of voluntary movements.
A neurodevelopmental condition involving differences in social communication and restricted or repetitive behaviours.
Immune-mediated inflammation affecting brain regions involved in movement and behaviour.
Inflammation of the brain caused by an immune response, sometimes producing seizures, movement changes and psychiatric symptoms.
A tick-borne infection caused by Babesia parasites that infect red blood cells.
Cancer arising in the urinary bladder, most commonly from its urothelial lining.
An inflammatory disease of small and medium-sized blood vessels, particularly in the limbs, that can restrict blood flow and cause pain, ulcers and gangrene.
A pattern of epileptic seizures that vary in frequency with phases of the menstrual cycle.
A blood clot in veins draining the brain that can cause headache, seizures and stroke.
Escape of cerebrospinal fluid through a defect in membranes surrounding the brain or spinal cord.
Spinal cord dysfunction caused by compression or other damage in the cervical spine.
Abnormal excessive movement between cervical vertebrae that can affect neural structures.
Narrowing of the spinal canal in the neck that may compress the spinal cord or nerve roots.
Degenerative changes affecting discs and joints of the cervical spine.
Inherited peripheral nerve disorders causing progressive weakness and sensory loss.
A migraine disorder with headache on at least 15 days per month, including migraine features on at least eight days, for more than three months.
A first episode of neurological symptoms suggestive of inflammatory demyelination in the central nervous system, which may or may not progress to multiple sclerosis.
A progressive neurological syndrome that can involve apraxia, rigidity and asymmetric movement problems.
Excessive movement or inadequate support at the junction of the skull and upper cervical spine.
A rapidly progressive prion disease affecting the brain.
A localised collection of pus caused by infection in or around a tooth.
An inflammatory disease affecting muscles and skin, often involving muscle weakness and characteristic rashes.
A group of metabolic disorders characterised by chronically elevated blood glucose, caused by insufficient insulin production, reduced insulin effectiveness or both.
Inflammation of colonic diverticula, sometimes causing abdominal pain, fever and bowel changes.
A historical term for abnormal fluid accumulation and swelling in body tissues. Once treated as a disease in itself, dropsy is now understood as a clinical manifestation that can arise from various underlying conditions.
An umbrella term for disorders involving dysfunction of the autonomic nervous system.
A movement disorder causing involuntary muscle contractions and abnormal postures or movements.
An inherited movement disorder associated with TOR1A variants causing sustained or twisting muscle contractions.
Inherited connective tissue disorders often involving joint hypermobility and tissue fragility.
A condition in which tissue resembling the uterine lining grows outside the uterus.
A neurological disorder characterised by an enduring predisposition to unprovoked epileptic seizures.
A mental health diagnosis involving deliberate falsification or induction of symptoms without obvious external rewards.
A chronic condition characterised by widespread pain, fatigue and other symptoms.
Rare inherited conditions associated with FLVCR1 gene variants affecting the retina and sometimes nervous system.
A rare speech disorder in which changes in pronunciation, rhythm and intonation cause a person's speech to be perceived as having a different accent. It can occur after neurological injury or alongside other neurological or speech disturbances.
A group of neurodegenerative disorders primarily affecting the frontal and temporal lobes, causing progressive changes in behaviour, language or movement.
A clinical diagnosis involving cognitive complaints attributed to altered cognitive functioning rather than an established neurodegenerative process.
Delayed gastric emptying without mechanical obstruction, potentially causing nausea, vomiting and early satiety.
A rare inherited prion disease causing progressive neurological deterioration.
An umbrella term for reported episodes of unexplained neurological and sensory symptoms among diplomatic, intelligence and other personnel. It does not establish a single disease or a confirmed underlying cause.
Involuntary contractions of muscles on one side of the face, commonly associated with facial nerve irritation.
A rare migraine subtype involving temporary motor weakness as part of the aura.
Brain dysfunction associated with liver failure or portosystemic shunting, causing changes in cognition and consciousness.
An inherited progressive neurological disorder affecting movement, cognition and behaviour.
Abnormally low blood glucose that can cause confusion, abnormal movements and seizures.
An illness commonly caused by Epstein–Barr virus, often involving fever, sore throat, swollen lymph nodes and fatigue.
A pancreatic neuroendocrine tumour that produces insulin and can cause recurrent hypoglycaemia.
A disorder of gut-brain interaction involving recurrent abdominal pain associated with changes in bowel habits.
Persistent or new symptoms following SARS-CoV-2 infection.
An infection caused by Borrelia bacteria transmitted through infected tick bites.
A group of cancers arising from lymphocytes, cells of the immune system.
A mood disorder involving persistent depressed mood or loss of interest alongside other symptoms that affect daily functioning.
A disorder involving recurrent episodes of mast-cell mediator release that can produce symptoms affecting multiple organ systems.
A condition involving compression of the coeliac artery and sometimes adjacent nerves by the median arcuate ligament.
A movement disorder involving involuntary contractions around the eyes and lower face.
An autoimmune condition with overlapping features of several systemic connective tissue diseases.
An immune-mediated disease of the central nervous system involving inflammatory demyelination.
A progressive neurodegenerative disorder affecting movement and autonomic functions.
A rare genetic disorder associated with ACTA2 variants affecting smooth muscle in blood vessels and other organs.
A chronic illness characterised by post-exertional malaise, substantial functional impairment and unrefreshing sleep.
An autoimmune neuromuscular junction disorder causing fluctuating, fatigable muscle weakness.
An inner-ear disorder associated with episodic vertigo, fluctuating hearing loss and tinnitus.
Kidney stones formed from crystallised substances in the urinary tract.
Neurological involvement from infection with Borrelia bacteria, including Lyme neuroborreliosis.
Inflammation of the nervous system caused by sarcoidosis.
Inflammation of the optic nerve, which may cause visual loss and eye pain.
Cancer arising from squamous cells lining the mouth, including the tongue.
Involuntary muscle contractions affecting the jaw, tongue or lower face.
A joint disorder involving cartilage and other joint tissue changes, often causing pain and stiffness.
A progressive neurological disorder affecting movement, often causing slowness, stiffness and tremor.
Brief attacks of involuntary movements often triggered by sudden voluntary movement.
Impaired coordination or function of pelvic floor muscles that can affect bowel, bladder or pelvic function.
Vitamin B12 deficiency caused by impaired absorption, often due to autoimmune loss of intrinsic factor.
A chronic vestibular disorder involving persistent non-spinning dizziness or unsteadiness, often worsened by upright posture, movement or complex visual stimuli.
A mental health condition that may develop after exposure to traumatic events, involving intrusive memories, avoidance and changes in arousal or mood.
A form of orthostatic intolerance involving an excessive increase in heart rate upon standing.
A progressive neurodegenerative condition affecting balance, eye movements and mobility.
Seizure-like episodes without the abnormal electrical brain activity of epileptic seizures.
MRI findings suggestive of central nervous system demyelination in a person without typical clinical symptoms of multiple sclerosis.
A psychiatric condition involving symptoms of psychosis alongside significant mood episodes.
Conditions associated with variants in the SCN9A sodium-channel gene, which can affect pain sensation and nervous system function.
Symptoms arising after reduction or cessation of serotonin reuptake inhibitor medication, including dizziness and sensory disturbances.
An autoimmune disease often affecting tear and saliva glands and sometimes nerves.
Damage to small sensory or autonomic nerve fibres.
A rare disorder associated with livedo racemosa and cerebrovascular disease, including strokes.
A rare neurological disorder involving progressive stiffness and painful muscle spasms.
Sudden brain injury caused by interrupted blood supply or bleeding in the brain.
Spinal cord damage often associated with vitamin B12 deficiency, affecting posterior and lateral columns.
Transient loss of consciousness due to reduced blood flow to the brain, usually followed by spontaneous recovery.
A systemic autoimmune disease that can affect multiple organs including the nervous system.
A condition in which abnormal fixation of the spinal cord causes stretching and neurological symptoms.
Brain dysfunction or injury caused by an external force to the head.
An autoimmune disease involving destruction of insulin-producing pancreatic beta cells and requiring insulin treatment.
Insufficient vitamin B12, which can cause anaemia and neurological injury including neuropathy and spinal cord dysfunction.
A contagious respiratory infection caused by Bordetella pertussis, characterised by prolonged coughing episodes.
An inherited disorder of copper metabolism affecting the liver, brain and other organs.