Neudle.com: hypotonia causes of

Differential
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abdominal distention

acetylcholine receptor antibody

acid maltase deficiency

acid maltase deficiency, adult

aciduria

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome, congenital

acquired immunodeficiency syndrome, infants and children

acrocyanosis

acromicria

acute intermittant porphyria

adrenoleukodystrophy

adverse drug reaction

agenesis of corpus callosum

Aicardi-Goutieres syndrome

airway obstruction

alcohol

alcohol, neurologic complications with

alternating hemiplegia

alternating hemiplegia of childhood

alveolar hypoventilation

aminoacidopathies

aminoacidurias

aminoacylase 1 deficiency

amitriptyline

amniocentesis

anemia

anemia, megaloblastic

Angelman syndrome

angiokeratoma

anorexia

anterior horn cell disease

antitoxin

antiviral agents

apnea

apraxia of eye movements

areflexia

aromatic amino acid decarboxylase deficiency

arrhythmia, cardiac

arthrogryposis multiplex

ascites

aspartate aminotransferase

aspartocyclase

ataxia

ataxia telangiectasia

attention deficit disorder with hyperactivity

atypical

autism

autonomic dysfunction

B 12 deficiency

B 12 deficiency, infants

Babinski sign in new born

bacterial infection

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavior, combative

behavioral disorder

benign congenital hypotonia

biotin deficiency, acquired

biotin deficiency, juvenile form

biotinidase deficiency

bone density, increased

bone marrow biopsy

bone marrow transplantation

botulinum toxin

botulism

botulism antitoxin

botulism immune globulin

Brown-Vialetto-Van Laere syndrome

brucellosis

brucellosis, nervous system involvement with

bulbar palsy

bulbar palsy, childhood

CAG repeats

calcification, intracranial

Canavan's disease

canned food

carcinoembryonic antigen

carcinoma

cardiac surgery, hypothermia and circulatory arrest for

cardiac surgery, neurologic complications with

cardiomyopathy

carnitine deficiency

carnitine deficiency myopathy

cataracts, congenital

cauda equina, enhancement

caudate nucleus, atrophy

celiac disease, childhood

central core disease

central hypoventilation, congenital

central nervous system, infection of

cerebellar ataxia, autosomal recessive

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar disease, eye movement disorder in

cerebellar hypoplasia

cerebellar vermis

cerebral cortical atrophy

cerebral palsy, associated problems with

cerebral vasculature

cerebral venous thrombosis

cerebro hepato renal syndrome

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, glycine

cerebrospinal fluid, protein of

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, red cells in

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, infancy and childhood

cerebrovascular accident, intrauterine

cerebrovascular accident, neonatal

cerebrovascular accident, postpartum

cervical spine injury

cherry red spot

chilbran skin lesions

chorea, Sydenham's, recurrent

chromosomal abnormality

chronic polyneuritis, children

chronic progressive external ophthalmoplegia

cirrhosis, infancy

Clinical Pathologic Conference(C.P.C.)

cobalamin C deficiency

Coffin-Siris syndrome

congenital heart disease

congenital heart disease, CNS complications with

congenital infection, CNS

congenital infection, viral

congenital malformation

congenital myopathy

congenital myopathy, inflammatory

congestive heart failure

cornea, opacification in infancy-causes of

cornea, opacity of

corpus callosum

corpus callosum, atrophy of

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cranial nerve enhancement

cranial neuropathy

cranial neuropathy, multiple

Craniosynostosis

creatine phosphokinase(CPK)elevated

cultured skin fibroblasts

cytochrome c oxidase, deficiency

cytomegalic inclusion disease

cytomegalovirus infection

cytomegalovirus infection, congenital

Dandy Walker malformation

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

delayed dentition

delivery, complicated

dementia

dementia, childhood

dentate nuclei

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

dermatitis

descending paralysis

developmental abnormality of brain

developmental disability

developmental evaluation

developmental milestones

developmental milestones, loss of

developmental retardation

differential diagnosis

digits, abnormal

diphtheria-tetanus-pertussis immunization

diplopia

disability, neurological

dislocated hip, congenital

dural sinus thrombosis

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electromyogram

electron microscopy

embolism, paradoxical

encephalopathy, acute

encephalopathy, anoxic

encephalopathy, neonatal

enzyme treatment

enzyme, defect

epidemiology of neurology

epileptic encephalopathy

evoked potentials

exome sequencing

eye movement, disorders of

facial anomalies

facial appearance, abnormal

facial expression abnormality

facial nerve palsy, bilateral

facial weakness

facial weakness, bilateral

fatty acid, elevated plasma content

feeding disorder

fetal alcohol syndrome

fetal movements, reduced

fetus

fever

fibrillations

fine motor function, impaired

fingernails, abnormal

fingernails, hypoplastic

fundus, abnormality of

gag reflex, depressed

gait disorder

gait, apraxic

galactosemia

gammaglobulin therapy, intravenous

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

genital hypoplasia

globus pallidus, hemorrhage

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

GLUT1

GLUT1 deficiency syndrome

gluten-free diet

glycine

glycogen storage disease

glycoprotein

Gowers maneuver

growth hormone deficiency

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, infantile and childhood form

hemorrhage, intracranial, newborn

hemorrhage, periventricular

hemorrhagic diathesis

Hirschprung's disease

histochemistry

histochemistry of muscle

Horner's syndrome, bilateral

Horner's syndrome, congenital

human genome

Hunter's syndrome

Huntington's chorea

Huntington's disease, children

hydrocephalus

hydrocephalus, communicating

hydrocephalus, congenital

hydrocephalus, exvacuo

hydroxyglutaric aciduria

hyperbilirubinemia

hyperbilirubinemia, CNS abnormality after

hyperpigmentation of skin

hyperpyrexia, CNS disorder causing

hypertrophic cardiomyopathy

hypodontia

hypogammaglobulinemia

hypopigmentation of skin

hypoxic encephalopathy

iatrogenic neurologic disorders

imbalance

immunization, neurologic complications with

immunodeficiency

immunosuppression

inappropriate antidiuretic(A.D.H.)hormone

inborn errors of metabolism

inclusion bodies

inclusion bodies, intracytopasmic

incoordination

infant, evaluation of

infantile hemiplegia

infantile neuronal degeneration

intellectual deterioration

interferon alpha

intestinal biopsy

intracranial hemorrhage

intracranial pressure, increased

intrauterine

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

kyphoscoliosis, neurologic causes of

lactic acidemia

leg weakness, bilateral

leukoencephalopathy, differential diagnosis

leukotrienes

lid closure, weakness of

lipid storage disorder of CNS

lissencephaly

listeria monocytogenes

liver disease

liver function enzymes

Lowe's syndrome

lumbar puncture

lymphoma

lysosomal storage disease

lysosomes, abnoral

macrocephaly

malabsorption

malformation, CNS, congenital

malformation, vascular

malignant hyperpyrexia

McArdle's disease

memory, impairment of

meningismus

meningitis, carcinomatous

meningitis, CSF cell count-normal

mental retardation

merosin

metabolic acidosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

methylene tetrahydrofolate reductase

methylenetetrahydrofolate reductase deficiency

methylmalonic acidemia

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

Middle east

migraine, seizures in

misdiagnosis

mitochondrial disease

mitral valve prolapse

movement disorder, extrapyramidal

movement disorder, hyperkinetic

MRI

MRI, abnormal

MRI, contrast enhanced

MRI, diffusion weighted

MRI, fetal

MRI, high signal foci on

MRI, susceptibility weighted

mucopolysaccharidoses

mucopolysacchariduria

multicore myopathy

multiminicore disease

multiple system atrophy

muscle atrophy, progressive

muscle atrophy, static

muscle biopsy

muscle diseases, characteristics of

muscle phosphorylase deficiency

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscle weakness, sudden onset of

muscle-eye-brain disease

muscular dystrophy

muscular dystrophy, cardiovascular changes with

muscular dystrophy, central nervous system abnormality

muscular dystrophy, congenital

muscular dystrophy, congenital, Fukuyama type

muscular dystrophy, LAMA2

myasthenia gravis

myasthenia gravis, neonatal

myopathy, centronuclear

myopathy, mitochondrial

myopathy, necrotizing

nemaline rod myopathy

neonatal infection, viral

neonatal intensive care unit

neonatal screening, genetic neurologic disorders

nerve conduction studies

nerve conduction studies, motor

nerve root enhancement

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neurocutaneous disease

neuroendocrinology

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic evaluation

neurologic signs

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction, abnormality of

neuronal ceroid-lipofuscinosis

neuronal migration disorder

neuroophthalmology

neuropathology

neuropathology, brain

newborn, evaluation of

obstetric neurologic injuries

ocular motility, disorders of

ocular myopathy

oculogyric crisis

old age, neurology of

opened mouth

ophthalmoplegia

ophthalmoplegia, neonatal

ophthalmoplegia, plus syndrome

ophthalmoplegia, progressive external

ophthalmoplegia, total

Oppenheim muscular dystrophy

optic atrophy

optic atrophy, infants

optic nerve

optic nerve, hypoplasia of

paraparesis, familial spastic

paraparesis, spastic

paraspinal muscle weakness

parenteral alimentation

paresthesias

Parkinson disease, dystonia with

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

pathology

patient information and support

pectus excavatum

pediatric neurology

periventricular leukomalacia

peroxisomal disease

peroxisomes

pertussis immunization

petechiae

phenylketonuria, variant form of

photophobia

PICU

placenta

placenta, infection of

placenta, thrombosis of

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

poison, neurologic problems with

poliomyelitis

poliomyelitis vaccine

POLR3B

polycystic kidneys

polyhydramnios

polymerase chain reaction

polymicrogyria

polymyositis

polymyositis, infantile

polysomnogram

Pompe's disease of glycogen storage

pons, atrophy

pons, lesion of

pontocerebellar atrophy

postoperative neurologic complications

postpartum

Prader-Labhart-Willi syndrome

precipitating factors

precocious puberty

pregnancy, neurologic complications in

premature infant

prenatal

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

progeria

prognosis

progressive muscular dystrophy

progressive neurologic disorder

psychiatric problems in neurologic disorders

psychomotor retardation

pupil, abnormality in neurologic disorders

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

quadriparesis

quadriparesis, acute

quadriplegia

radiation hypersensitivity

radiculitis

ragged-red fibers

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

rash

recurrent

reflex, stretch

reflex, tonic stretch

Refsum's disease

renal failure

renal tubular acidosis

repetitive nerve stimulation

respirations in CNS disease

respirator

respiratory arrest

respiratory depression

respiratory distress syndrome, neurologic status with

respiratory failure

respiratory tract infection

riboflavin transporter deficiency

saccadic eye movements, abnormal

scoliosis

scoliosis, neurologic association with

screaming

screening

segmental demyelination

seizure

seizure, children

seizure, focal

seizure, injury following

seizure, neonatal

self-mutilation

semialdehyde dehydrogenase deficiency

sensorineural hearing loss

septicemia

serum alanine aminotransferase

short stature

shunt procedure, ventricular

skin, biopsy

skin, lesions in neurologic disorders

skull x-ray, abnormal

sleep

sleep pathology and physiology

small for dates infant, problems in

SMN1 gene

sodium valproate

sodium valproate, toxicity

spastic diplegia

spasticity

speech disorder, childhood

speech, delayed development of

spinal cord, enlargement

spinal cord, injury of

spinal cord, injury, New Born

spinal cord, intramedullary cyst of

spinal cord, transection

spinal muscular atrophy

spinal muscular atrophy, classification

spinocerebellar ataxia

splenomegaly

spongy degeneration of brain

steroid therapy, CNS treatment and complications with

stillbirth

strabismus

streptococcal infection

subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease

subdural effusion

subdural hematoma, neonates and infants

subgaleal hematoma

suck, poor

sudden death

sulfite oxidase deficiency

superior sagittal sinus thrombosis

symmetric brain lesions

systemic lupus erythematosus

systemic lupus erythematosus, neonatal

systemic lupus erythematosus, neurologic complications with

teeth, number of in infants

telangiectases

temper tantrums

temporalis muscle wasting

tongue, fasciculations of

tongue, protrusion of

tongue, weakness

tonic spasms

toxic encephalopathy

toxins, nervous system

toxoplasmosis, CNS

tracheostomy

transient loss of muscle tone

transient neurologic deficit

transilumination of skull

treatment of neurologic disorder

trinucleotide repeats

type 1 muscle fiber

ultrasonography

ultrasonography, head

ultrasonography, head, fetus-neonate

uric acid, low

urinalysis, abnormal

urinary incontinence

urine test for metabolic disorders

vaccination, neurologic complications with

vision, failure of in childhood

visual evoked response

Walker-Warburg syndrome

walking, difficulty with

weakness

weakness, acute

weakness, congenital

weakness, generalized

weakness, infant

weakness, progressive

weakness, proximal

weight loss

Werdnig-Hoffman disease

Wernicke's encephalopathy

x-linked mental retardation

Showing articles 100 to 132 of 132 << Previous

Ultrastructural, Neurological, & Glycosaminoglycan Abnormalities in Lowe's Syndrome
Ann Neurol 16:40-49, Wisniewski,K.E.,et al, 1984

The Cerebrohepatorenal (Zellweger) Syndrome
NEJM 310:1141-1146, Moser,A.E.,et al, 1984

The Causes of Cerebral Palsy
JAMA 247:1473-1477, Holm,V.A., 1982

Hypomelanosis of Ito (incontinentia pigmenti achromians) :Macrocephaly & Gray Matter Heterotopias
Neurol 32:1013-1016, Ross,D.L.,et al, 1982

The Neuropathology of Glycine Encephalopathy:Five Cases with Immunohistochemical & Ultrastructural Observations
Neurol 32:975-985, Agamanolis,D.P.,et al, 1982

Clin. Path. Conference
Osteopetrosis, Malignant Juvenile Form, Case Record 37-1982, NEJM 307:735-74382., , 1982

Neurological Manifestation of Accidental Hypothermia
Ann Neurol 10:384-387, Fischbeck,K.H.,et al, 1981

Biotin-Responsive Carboxylase Deficiency Associated With Subnormal Plasma & Urinary Biotin
NEJM 304:817-820, Thoene,J.,et al, 1981

Biotin Deficiency:An Unusual Complication Of Parenteral Alimentation
NEJM 304:820-823, Mock,D.M.,et al, 1981

Human Cerebellar Hypoplasia, A Syndrome of Diverse Causes
Arch Neurol 37:300-305, Sarnatt,H.B.,et al, 1980

Congenital Myotonic Dystrophy
Arch Neurol 37:693-696, Argov,Z.,et al, 1980

Subgaleal Hematoma, A Complication of Instrumental Delivery
JAMA 244:1597-1598, Plauche,W.C., 1980

Infantile Neuronal Degeneration Masquerading as Werdnig-Hoffmann Disease
Ann Neurol 8:317-324, Steiman,G.S.,et al, 1980

Intracranial Hemorrhage in the Newborn:Current Understanding & Dilemmas
Neurol 29:632-635, Volpe,J.J., 1979

Neonatal Myasthenia Gravis in the Infant of a Myasthenic Mother in Remission
Ann Neurol 6:72-75, Elias,S.B.,et al, 1979

Nemaline (Rod) Myopathy:The Need for Histochemical Evaluation of Affected Families
Ann Neurol 4:37, Bender,A.N.,et al, 1978

Glycine Encephalopathy
NEJM 298:687, Ch'ien,L.T., 1978

A Synd of Methylmal Acid, Homocystinuria, Megaloblas. Anemia & Neurol Abnor. in a Vit B-12-def Breast-fed Infant of veget
NEJM 299:317, Higginbottom,M.C., 1978

Hyperphenylalaninemia Due To A Deficiency of Biopterin
NEJM 299:673-679, Stanley,S.K.,et al, 1978

The Lissencephaly, (Agyria) Syndrome in Siblings
Arch Neurol 35:608-611, Garcia,C.A.,et al, 1978

Fatal Infantile Form of Muscle Phosphorylase Deficiency
Neurol 28:1124-1129, DiMauro,S.,et al, 1978

Adverse Effects on Offspring of Maternal Alcohol Abuse During Pregnancy
NEJM 297:528, Ouellette,E.M.,et al, 1977

Guillain-Barre Syndrome with Hydrocephalus in Early Infancy
Arch Neurol 34:567, Gilmartin,R.C.,et al, 1977

Neonatal Ophthalmoplegia with Microfibers:A Reversible Myopathy
Neurol 27:974, Hanson,P.A.,et al, 1977

Globoid cells, Glial nodules, & Peculiar Fibrillary Changes in the cerebro-hepato-renal Syndrome of Zellweger
Ann Neurol 2:473, deLeon,G.A.,et al, 1977

Prader-Willi-Syndrome, In Endocrine & Genetic Diseases of Childhood & Adolescence
(Ed) , 1975. W. B. Saunders Co, p, Gardner,L.I., 1975

Lumbosacral Radiculomyelitis Assoc with Pandemic Acute Hemorrhagic Conjunctivitis
Letter Lancet Feb 1973., Wadia,N.H.,et al, 1973

Congenital Dystrophia Myotonica
Neurol 22:443, Dyken,P.D., 1972

The Neuropathy of Acute Intermittent Porphyria
Quart J Med 38:307, 1969 July., Ridley,A., 1969

The Hypotonic Infant
Med Progress 64:422, Rabe,E., 1964

Neuro CPC of MGH
Congenital Toxoplasmosis Involving CNS, NEJM 269:369-3741963., , 1963

Neuro CPC of MGH
Myopathy, Severe, Generalized, Chronic, NEJM 258:388-3938., , 1958

Neurology & Psychiatry Section-Year book of Pediatrics
Pediatr Abstract p. 406-449., , 1850

Showing articles 100 to 132 of 132 << Previous