Neudle.com: "Talpes equinovarus"

Differential
(Click to cross reference)

airway obstruction

anosmia

areflexia

arrhythmia, cardiac

arthrogryposis multiplex

autonomic dysfunction

autonomic neuropathy

autonomic neuropathy, idiopathic

Babinski sign

benign essential tremor

cataracts, congenital

central core disease

cervical spine

cervical spine abnormality

chromosomal abnormality

chromosome 17

chromosome 9

clubfoot as related to neurologic disease

congenital bilateral perisylvian syndrome

congenital malformation

congenital myasthenic syndromes

corpus callosum, thinning

creatine phosphokinase(CPK)elevated

deafness

deep tendon reflexes

developmental abnormality of brain

developmental retardation

diabetes insipidus

diabetes mellitus

diabetes mellitus, ocular complications in

diabetic cranialneuropathies

dislocated hip, congenital

distal muscle atrophy

distal muscle weakness

dopa responsive dystonia

drooling

dysarthria

dyskinesia

dyskinesia, buccal lingual facial

dyskinesia, causes of

dyskinesia, drug induced

dysmorphic

dysphagia

dystonia

dystonia musculorum deformens

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electromyogram

Emery-Dreifuss muscular dystrophy

facial weakness, bilateral

familial

fatigue

fine motor function, impaired

gag reflex, depressed

genetic neurologic disorders

genetic testing

Gilles de la Tourette syndrome

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

Hallervorden Spatz disease

hepatolenticular degeneration(Wilson's disease)

hypogonadism, hypogonadotropic

intellectual deterioration

intrinsic hand muscles, wasting of

iritis

iron, brain

kyphoscoliosis, neurologic causes of

kyphosis

L-dopa

leg weakness, bilateral

light-near dissociation, causes of

lordosis

malformation, CNS, congenital

malignant hyperpyrexia

mental retardation

mestinon

micrognathia

mitral valve prolapse

multiple endocrine neoplasia

muscle atrophy, progressive

muscle atrophy, static

muscle biopsy

muscle cramp

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, Becker

nerve conduction studies

nerve hypertrophy

neuroendocrinology

neurologic disease, diagnoses of

neuroma

neuropathy

neuropathy, ataxic

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, onion bulb

neuropathy, peripheral

neuropathy, sensory

neuropathy, sensory, hereditary

nystagmus, upbeating-in primary position of gaze

nystagmus, vertical

opened mouth

operculum syndrome, bilateral

paraparesis, familial spastic

paraparesis, spastic

Parkinson disease

Parkinson disease, juvenile

Parkinsonism syndrome

peroneal muscle atrophy, causes of

polyneuropathy, familial

pupil, abnormality in neurologic disorders

pupil, light reflex, abnormal

pyramidal tract dysfunction

scoliosis, neurologic association with

seizure

sensorineural hearing loss

sensory loss

skin, lesions in neurologic disorders

temporalis muscle wasting

term infant

torticollis

treatment of neurologic disorder

tremor

trinucleotide repeats

uveitis

vibratory sensation, abnormal

visual acuity, decreased

visual evoked response

visual fields, constricted

x-ray, cervical spine

Showing articles 0 to 22 of 22

A Child with Arthrogryposis
Neurol 91:e995-e998, Irumudomom, O. & Ghosh, P.S., 2018

A Neonate with Micrognathia and Hypotonia
Neurol 86:e80-e84, Vawter-Lee, M.M.,et al, 2016

CMT with Pyramidal Features
Neurol 60:696-699, Vucic,S.,et al, 2003

Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996

Charcot-Marie-Tooth Disease and Related Inherited Neuropathies
Medicine 75:233-250, Murakami,T.,et al, 1996

Charcot-Marie-Tooth Neuropathies:From Clinical Description to Molecular Genetics
Muscle & Nerve 18:267-275995., Ionasecu,V.V., 1995

Autosomal Dominant, Familial Spastic Paraplegia, Type I:Clinical and Genetic Analysis of a Large North American Family
Neurol 45:325-331, Fink,J.K.,et al, 1995

Hereditary Sensory and Autonomic Neuropathy with Cataracts, Mental Retardation, and Skin Lesions:Five Cases
Neurol 45:1405-1408, Heckmann,J.M.,et al, 1995

The Neurologic Syndrome of Vitamin E Deficiency:A Significant Cause of Ataxia
Neurol 43:2167-2169, Kayden,H.J., 1993

Congenital Bilateral Perisylvian Syndrome:Study of 31 Patients
Lancet 341:608-612, Kuzniecky,R.,et al, 1993

Friedreich Ataxia
In Rowland, L. P. Merritt's Textbook of Neurology, 8th Ed, Lea & Febiger, Phila, Ch 13, p627, Rosenberg,R.N., 1989

Refsum Disease
In Rowland's Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8thEd, p. 509, Menkes,J.H., 1989

Rigid Spine Syndrome and Rigid Spine Sign in Myopathies
J Child Neurol 4:273-282, Merlini,L.,et al, 1989

Neurologic Findings in Men with Isolated Hypogonadotropic Hypogonadism
Neurol 39:223-226, Schwankhau,J.D.,et al, 1989

MR Imaging of a Group I Case of Hallervorden-Spatz Disease
J Comput Assist Tomogr 12:851-853, Mutoh,K.,et al, 1988

Central Core Disease, Clinical Features in 13 Patients
Medicine 66:389-396, Shuaid,A.,et al, 1987

Hereditary Dystonia-Parkinsonism Syndrome of Juvenile Onset
Neurol 36:1424-1428, Nygaard,T.C.&Duvoisin,R.C., 1986

Multiple Endocrine Neoplasia, Type 2b:Phenotype Recognition; Neurological Features & Their Pathological Basis
Ann Neurol 6:302-314, Dyck,P.J.,et al, 1979

The Spectrum of Mild X-Linked Recessive Muscular Dystrophy
Arch Neurol 34:408, Ringer,S.P.,et al, 1977

Juvenile Diabetes Mellitus & Optic Atrophy
Arch Neurol 34:759, Lessell,S.,et al, 1977

Charcot-Marie-Tooth Disease Associated With"Essential Tremor"
Neurol Sciences 28:17-40, Salisachs,P.J., 1976

Clinical Diagnosis of the Dyskinesias
Med Clin of North Am 56:1321, Duvoisin,R., 1972

Showing articles 0 to 22 of 22