Neudle.com: spastic ataxia

Differential
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abdominal reflex, absent

achilles tendon, enlarged

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome myelopathy

acromicria

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adult polyglucosan body disease

adult-onset leukodystrophy, with neuroaxonal spheroids

advances in neurology

Africa

alcohol intolerance

alcohol, neurologic complications with

alcoholism

Alexanders disease

Alexanders disease, adult onset

algorithm

alopecia

alternating rapid movement

aneurysm, vertebral basilar system

angiitis, granulomatous of CNS

angiography, spinal

ankle reflex, absent

anterior horn cell disease

antioxidant

aphasia

areflexia

Arnold Chiari malformation

atherosclerosis, generalized

atherosclerosis, premature

atypical

auditory evoked brainstem potentials

autism

autoantibodies

autoimmune disease

autonomic dysfunction

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

basal ganglia, calcification of

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

brachial plexus neuropathy

brain biopsy

brain biopsy, negative

brain biopsy, stereotaxic

brainstem

brainstem, atrophy

brainstem, glioma

brainstem, glioma in children

brainstem, glioma, adult

brainstem, ischemia

brainstem, lesion of

brainstem, neoplasms of

brucellosis

brucellosis, nervous system involvement with

calcification, intracranial

cane

carcinoma of pancreas

CAT scan

CAT scan, abnormal

CAT scan, emission

CAT scan, emission, abnormal

cataracts

cataracts, congenital

caudate nucleus, atrophy

caudate nucleus, lesion of

caudate nucleus, lesion of, bilateral

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar hemangioma

cerebellar lesion

cerebellar plaques, amyloid

cerebellar vermis

cerebral cortical atrophy

cerebral folate deficiency syndrome

cerebral palsy

cerebral palsy, associated problems with

cerebral venous thrombosis

cerebroretinal microangiopathy with calcifications and cysts

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, lactic acid concentration

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, recurrent

cerebrovascular disease

cervical myelopathy

cervical spondylosis

chenodeoxycholic acid

choroid plexus, tumor of

chromosomal abnormality

chromosome 2

chromosome 6

chronic progressive external ophthalmoplegia

cirrhosis

Clinical Pathologic Conference(C.P.C.)

clonus

clubfoot as related to neurologic disease

cobalamin C deficiency

coccidioidomycosis

cognition

cold hands sign

color vision, impaired

coma

concentration, impaired

confusion

congenital infection, CNS

consanguinity

constipation

controversies in neurology

conversion reaction

corpus callosum, atrophy of

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

crossed adductor reflex

crying, pathologic

cryptococcal meningitis

cyst, epidermoid of CNS

cysticercosis

deafness

degenerative diseases of CNS

dementia, rapidly progressive

dementia, reversible

dementia, treatment of

demyelinating disease

dentate nuclei, lesion of

depression

dermatitis

dermatomyositis

developmental milestones

developmental milestones, loss of

developmental retardation

differential diagnosis

diplegia, spastic cerebral

diplopia

disability, neurological

disorientation

distal muscle atrophy

Dravet syndrome

drug abuse

drug abuse, inhalation

drug abuse, neurologic complications of

dysarthria

dysarthria-clumsy hand syndrome

dystonia musculorum deformens

dystonia, cervical

dystrophic calcification

ears of the Lynx MR sign

eczema

electrical sensation

electroencephalogram, abnormalities of

enzyme, muscle disease

ependymoma

epicanthal folds

epidemiology of neurology

epileptic encephalopathy

equinovarus

evoked potentials

executive dysfunction

exome sequencing

eye movement, disorders of

facial appearance, abnormal

facial nerve palsy

facial nerve palsy, recurrent

fatal familial insomnia

fatigue

fatty acid, elevated plasma content

fever

fine motor function, impaired

finger nose finger test

finger tapping

fistula, arterio-venous

fistula, arterio-venous, dural

fistula, arterio-venous, dural, spinal

fluorescent treponema antibody absorption(FTA-ABS)

folic acid

folic acid deficiency

foot deformity

frataxin

Friedreich's ataxia

Friedreich's ataxia, late onset

fundus, abnormality of

gadolinium

gait disorder

gait, spastic

gammaglobulin therapy, intravenous

genetic neurologic disorders

genetic screening

genetic testing

geographic location

Gerstmann-Straussler-Scheinker disease

GFAP gene

girdle sensation

glioblastoma multiforme(astrocytoma Gr.III)

glioma

glioma, low-grade

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glucagonoma

GLUT1 deficiency syndrome

glutamic acid decarboxylase, antibody

glycogen storage disease

growth retardation

Guillain Barre syndrome

Hallervorden Spatz disease

hearing problems in children

heel-knee-shin test

hemiparesis

hemosiderosis of CNS, superficial

hepatic failure

hepatitis

hepatolenticular degeneration, non-Wilsonian

human immunodeficiency virus type 1

human T-lymphotropic virus type I(HTLV-I)

human T-lymphotropic virus type II(HTLV-II)

Huntington's chorea

Huntington's disease, children

hydrocephalus

hyperammonemic encephalopathy

hyperhidrosis

hyperhomocysteinemia

hyperpigmentation of skin

hypoglycorrhachia, causes of

hypomyelination

hypotension, systemic

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic intranuclear

intellectual deterioration

intrinsic hand muscles, wasting of

iron, brain

irritability

Jakob-Creutzfeldt disease

leg weakness, bilateral

Leigh's disease

Leigh's disease, adult variety

lenticular nucleus, lesion of, bilateral

leptospirosis

leukemia, neurologic findings assoc.with

leuko-araiosis

leukodystrophy

leukoencephalopathy

leukoencephalopathy, differential diagnosis

level of consciousness, decreased

lymphoma involving CNS

Marinesco-Sjogren syndrome

medulla oblongata, lesion of

megalencephaly

Melkersson's syndrome

memory, defect of recent

memory, impairment of

meningeal biopsy

meningeal gliomatosis

meningitis

meningitis, actinomycotic

meningitis, aseptic

meningitis, bacterial

meningitis, blastomyces

meningitis, brucellosis

meningitis, candida

meningitis, carcinomatous

meningitis, chronic

meningitis, chronic benign lymphocytic

meningitis, cladosporium

meningitis, coenurosis

meningitis, CSF cell count-normal

meningitis, cysticercosis

meningitis, echinococcal

meningitis, eosinophilic

meningitis, fungal

meningitis, helminthic

meningitis, histoplasma

meningitis, leptospira

meningitis, lymphomatous

meningitis, Mollaret's

meningitis, nocardia

meningitis, paracoccidioides

meningitis, post myelography

meningitis, recurrent

meningitis, syphilitic

meningitis, TB

meningitis, toxoplasma

meningoencephalitis

meningoencephalitis, toxoplasma

meningomyelitis

mental retardation

mental status, abnormal

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

methyl benzene

methylglutaconic aciduria

methylmalonic acidemia

microangiopathy, brain

microcephaly

microdontia

middle cerebellar peduncle

middle cerebellar peduncle, lesion, bilateral

misdiagnosis

mitochondrial disease

molecular genetics

mononeuritis multiplex

mortality

motor neuron disease

movement disorder

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, brachial plexus

MRI, contrast enhanced

MRI, diffusion weighted

MRI, emergent

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, negative

MRI, paramagnetic effect

MRI, spinal cord

MRI, spine

MRI, T1 weighted high signal foci

MRS

multiple sclerosis

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle pain

muscle stiffness

muscle weakness

muscle weakness, proximal

myelopathy, chronic progressive

myelopathy, hepatic

myelopathy, tract-specific

myxedema, neurologic manifestations of

Native Americans

neoplasm, primary intracerebral

neoplasm, primary of CNS

neoplasm, primary of CNS-classification

neoplasm, primary of CNS-metastasizing to subarachnoid space

neoplasm, primary of CNS-treatment of

nerve biopsy

nerve conduction studies

neurocutaneous disease

neuroendocrinology

neurogenic bladder

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic examination

neurologic examination, focal

neurologic signs

neurologic symptoms

neuronal intranuclear inclusion disease

neuropathology

neuropathology, brain

neuropathy

neuropathy, demyelinating

neuropathy, peripheral

neuropathy, sensory

neurosyphilis

neurotoxin

next-generation sequencing

night blindness

nitrous oxide

numb clumsy hands syndrome

ocular motility, disorders of

oculodentodigital dysplasia

oculogyric crisis

ophthalmoplegia

ophthalmoplegia, progressive external

optic ataxia

optic atrophy

optic atrophy, hereditary

optic neuritis

optic neuropathy

optical coherence tomography

orthostatic hypotension

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

paraparesis, spastic, tropical

Parkinson disease, arteriosclerotic

Parkinson disease, asymmetric onset

Parkinson disease, L-dopa nonresponsive

Parkinson disease, tremor, absence of

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

photosensitivity, skin

pinealoma

pleocytosis of cerebrospinal fluid

POLR3B

polyglucosan body

polyglucosan body disease

polymerase chain reaction

posterior column disease

postural abnormality

precipitating factors

primary lateral sclerosis

prion disease

prisoners of war, neurologic complications in

prognosis

progressive neurologic disorder

proprioception, abnormal

pseudobulbar palsy

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychomotor retardation

psychosis

ptosis

pursuit eye movements, abnormal

pyramidal

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriparesis

quadriparesis, progressive

quadriplegia

radiation therapy, CNS treatment and complications with

radiculopathy

Rankin score

rapidly progressing neurologic illness

remote effect of cancer on the nervous system

renal stones

reticulum cell sarcoma

retinal detachment

retinitis pigmentosa

Rett's syndrome

reversible neurologic disorder

rubella encephalitis, progressive

rubella syndrome

rubella virus

saccadic eye movements, abnormal

sclerae, hyperpigmented

scleroderma

scleroderma, neurologic involvement with

SCN1A gene

scoliosis

scoliosis, neurologic association with

scotoma

screening

sea-blue histiocytes

sedimentation rate, elevated

seizure, tonic-clonic

sensorineural hearing loss

sensory level

sensory loss

sensory loss, cutaneous

serologic testing

serologic testing of cerebrospinal fluid

short stature

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, darkening of

skin, lesions in neurologic disorders

skull x-ray, abnormal

sleep apnea

sleep pathology and physiology

slow virus infection of CNS

sodium channel dysfunction

solitary scerlosis

somatosensory evoked potentials

spastic paraplegia, type 11

spastic paraplegia, type 7

spasticity

spastin

speech disorder

speech disorder, childhood

speech, loss of

spinal cord

spinal cord, cervical

spinal cord, compression of

spinal cord, lesion of

spinal cord, pathologic exam of

spinal cord, vascular malformation of

spinal xanthomatosis

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar ataxia type 7

spinocerebellar degeneration

spondylolysis

spongy degeneration of brain

striatonigral degeneration

striatonigral degeneration, infantile

subcortical U fibers

substantia nigra

superior cerebellar peduncle

symmetric brain lesions

syndactyly

syphilis, diagnosis and treatment

syphilis, meningomyelitis

syphilis, neurologic complications with

teeth, number of in infants

tone, muscle, increased

tongue, enlarged

tongue, impaired movements of

tonsillar herniation of cerebellum

toxins, nervous system

toxoplasmosis, acquired

toxoplasmosis, CNS

transient ischemic attack

treatment of neurologic disorder

tremor

tremor, cerebellar

tremor, intention

trinucleotide repeats

ulcerative colitis

ulcers, fingertip

upgaze, paralysis of

urea-cycle enzymopathies

vibratory sensation, abnormal

visual acuity, decreased

visual evoked response

visual loss

vitamin deficiency

vitiligo

Vogt-Koyanagi-Harada syndrome

walking frame

walking, difficulty with

war

weakness

weakness, progressive

weakness, proximal

weight loss

Western immunoblot test

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