Neudle.com: coarse facies

Differential
(Click to cross reference)

abortion, spontaneous

acromegaly

acromicria

adrenoleukodystrophy

adverse drug reaction

agenesis of corpus callosum

aggression

alcohol

alcohol, neurologic complications with

alveolar hypoventilation

angiography, cerebral

angiokeratoma

ankle edema

anosmia

anticoagulant, complications of

anticonvulsants

anticonvulsants, blood level determination of

anticonvulsants, teratogenicity of

anticonvulsants, untoward effects of

attention deficit disorder with hyperactivity

attention span

atypical

autism

autonomic dysfunction

Babinski sign

baldness

basal ganglia, calcification of

bone density, increased

bone marrow transplantation

brachial neuritis

brachial neuritis, acute

brachial neuritis, bilateral

brachial plexus neuropathy

brachial plexus neuropathy, bilateral

brachial plexus neuropathy, familial

brachial plexus neuropathy, recurrent

calcification, intracranial

carbamazepine

cardiomyopathy

caries

carpal tunnel syndrome

CAT scan

CAT scan, abnormal

cataracts

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar vermis

cerebral arteries

cerebral cortical atrophy

cerebral infarction

cerebral vasculature

cerebro hepato renal syndrome

cerebrovascular accident

cerebrovascular accident, infancy and childhood

cerebrovascular accident, young adult

cerebrovascular disease

ceruloplasmin, serum

chewing, impaired

children

chondrodysplasia punctata

chromosomal abnormality

chronic graft versus host disease

cisterna magna, enlarged

cleft lip

cleft palate

Clinical Pathologic Conference(C.P.C.)

clinodactyly

clubfoot as related to neurologic disease

Cockayne's syndrome

codfish vertebrae

Coffin-Siris syndrome

cold temperature

collagen vascular disease

congenital birth defects

congenital heart disease

congenital heart disease, CNS complications with

congenital malformation

congenital malformation, dilantin therapy causing

congenital malformation, non CNS

cornea, opacification in infancy-causes of

cornea, opacity of

Cornelia de Lange syndrome

corpus callosum

corpus callosum, atrophy of

cost effectiveness

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

cry, abnormal

cry, weak

cryptorchidism

cultured skin fibroblasts

cyanosis

cyst, porencephalic

cystinuria

Dandy Walker malformation

developmental abnormality of brain

developmental retardation

diabetes mellitus

diet

differential diagnosis

dislocated hip, congenital

dissociated sensory loss

distal muscle weakness

DNA probes

doppler, transcranial

drooling

dropped head syndrome

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

epidermal nevus syndrome

facial appearance, abnormal

facial expression abnormality

facial hypoplasia

facial nerve palsy

facial weakness

facial weakness, bilateral

fatty acid, elevated plasma content

feeding disorder

fetal alcohol syndrome

fetal valproate syndrome

fetus

fingernails, abnormal

fingernails, hypoplastic

fish

fluorescene in situ hybridization

fragile-X syndrome

fragile-X syndrome, carrier

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

growth hormone deficiency

hemorrhage, intracranial, newborn

hemorrhage, periventricular

hemorrhagic diathesis

hepatic encephalopathy

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

hepatomegaly

hepatosplenomegaly

heralding manifestation

heterotopia

high arched palate

hirsutism

histochemistry of muscle

hyperpigmentation of skin

hypertrophic cardiomyopathy

hypopigmentation of skin

hypoplastic left heart syndrome

hyporeflexia

hypotelorism

hypothyroidism

hypothyroidism, congenital

inclusion bodies, intracytopasmic

infant, evaluation of

infection, recurrent

insulin resistance

intellectual deficit

intellectual deterioration

intelligence quotient

intracranial hemorrhage

intracranial pressure, increased

Kayser-Fleischer ring

Krabbe's disease

kyphoscoliosis, neurologic causes of

kyphosis

laughing, pathologic

learning disability, in children

leg weakness, bilateral

lid closure, weakness of

life expectancy

lip, abnormal

lipid storage disorder of CNS

lissencephaly

livedo reticularis

liver function enzymes

low birth weight

lysosomal storage disease

lysosomes, abnoral

macrocephaly

macrognathia

malformation, CNS, congenital

malformation, vascular

masked facies

melanomatosis, primary malignant

mental retardation

mental retardation, familial

metabolic disorder, primary

metachromatic leukodystrophy

middle cerebellar peduncle

middle cerebellar peduncle, lesion, bilateral

midline defect in children

misdiagnosis

mitral valve lesion

molecular genetics

molybdenum cofactor deficiency

mucopolysaccharidoses

mucopolysacchariduria

multicore myopathy

multiple system atrophy

muscle atrophy, focal

muscle atrophy, progressive

muscle biopsy

muscle diseases, characteristics of

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, cardiovascular changes with

muscular dystrophy, congenital

muscular dystrophy, LAMA2

myotonia dystrophica, classification

myxedema, neurologic manifestations of

neoplasm, metastatic to CNS

neuroendocrinology

neuroichthyosis

neurologic disease, diagnoses of

neurologic evaluation

neurologic signs

neurologic symptoms

neuropathology

neuropathology, brain

neuropathy

neuropathy, hereditary peripheral

newborn, evaluation of

oculodentodigital dysplasia

oligodactyly

opened mouth

ophthalmoplegia

ophthalmoplegia, progressive external

ophthalmoplegia, total

optic atrophy

optic nerve

optic nerve, hypoplasia of

optic neuropathy

oropharyngeal weakness

osteogenesis imperfecta

palpebral fissure, short

Parkinson disease, atypical

percussion induced muscle contraction

periodic paralysis

periventricular leukomalacia

philtrum, hypoplastic

phocomelia

photosensitivity, skin

pigmentary retinopathy

Prader-Labhart-Willi syndrome

precipitating factors

pregnancy, anticonvulsants during

pregnancy, neurologic complications in

premature infant

prenatal

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

progeria

prognathism

prognosis

progressive supranuclear palsy

prolactin, elevated

prosopometamorphopsia

proximal muscle atrophy

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychomotor retardation

pupil, abnormality in neurologic disorders

pupil, ectopic-congenital

pyramidal tract dysfunction

scoliosis, neurologic association with

seizure, injury following

seizure, intractable

seizure, neonatal

seizure, pregnancy

sensorineural hearing loss

skin, lesions in neurologic disorders

skull x-ray, abnormal

skull x-ray, bony defect on

slit lamp examination

smiling

sodium valproate

sodium valproate, toxicity

Southern immunoblot test

speech disorder

speech disorder, childhood

speech, delayed development of

spinal cord, compression of

splenomegaly

stem cell transplantation

symmetric brain lesions

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

teratogenesis

teratogenic drugs

term infant

testicular enlargement

thrombocytopenia

titinopathy

tongue, enlarged

tongue, protrusion of

transverse smile

treatment of neurologic disorder

tremor

tremulousness

trichopoliodystrophy

trientine dihydrochloride

trigeminal nerve, lesion of

trigeminal neuropathy

trimethadione

trinucleotide repeats

voice, abnormality of

weakness, generalized

weakness, progressive

x-linked mental retardation

zinc

Showing articles 50 to 67 of 67 << Previous

Coffin-Siris Syndrome, Neuropathologic Findings
Arch Neurol 42:350-353, DeBassio,W.A.,et al, 1985

Fragile X Syndrome:Associated Neurological Abnormalities & Developmental Disabilities
Ann Neurol 18:665-669, Wisniewski,K.E.,et al, 1985

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

Sclerosteosis:Neurogenetic & Pathophysiologic Analysis of an American Kinship
Neurol 33:267-277, Stein,S.A.,et al, 1983

Dominant Chondrodysplasia Punctata with Neurologic Symptoms
Neurol 33:1095-1097, Curless,R.G., 1983

Clinicopathological Conference
Maroteaux-Lamy Syndrome, Case 44-1983, NEJM 309:1109-1117983., , 1983

Fragile X Chromosome & X-Linked Mental Retardation
CMA Journal 127:123-126, Larbrisseau,A.,et al, 1982

Brain Abnormalities in Infants with Fotter Syndrome (oligohydramnios tetrad)
Neurol 31:1571-1574, Grunnet,M.L.,et al, 1981

Hazards of Oral Anticoagulants During Pregnancy
JAMA 243:1549-1551, Stevenson,R.E.,et al, 1980

Fetal Alcohol Syndrome & Related CNS Problems
Neurol 29:1429-1430, Wisniewski,K.,et al, 1979

Cockayne Syndrome:Unusual Neuropathological Findings & Review of the Literature
Ann Neurol 6:340-348, 1979, Soffer,D.,et al, 1979

The Pregnant Epileptic, A Review & Recommendations
Arch Neurol 36:601-603, Montouris,G.D.,et al, 1979

Agenesis of the Corpus Callosum:A Study of the Frequency of Associated Malformations
Ann Neurol 6:349-354, Parrish,M.L.,et al, 1979

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

Osteogenesis Imperfecta, in Heritable Disorders of Connective Tissue
(Ed) , 4th edition, The C. V. Mosby Company St. Louis, Chap. 8, pp. 390. , 1972, McKusick,V.A., 1972

Familiar Basilar Impression
Neurol 22:554, Paradis,R.,et al, 1972

Diagnostic Significance of Median Facial Anomalies for Holoprosencephaly
Pediatr 256, 1964 Aug., DeMeyer,W.,et al, 1964

The Cornelia de Lange Syndrome
J Pediatr 63:1000-1020, Ptacek,L.J., 1963

Showing articles 50 to 67 of 67 << Previous