Neudle.com: ptosis hereditary

Differential
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abdominal distention

abducens nerve paralysis

altered states of consciousness

alveolar hypoventilation

autonomic dysfunction

baldness

basal ganglia, calcification of

blood dyscrasias, neurologic findings with

brainstem, dysfunction

cachexia

calcification, intracranial

CAT scan, false negative

cataracts

central core disease

cerebellar ataxia, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebral cortical atrophy

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, pressure low

cerebrovascular accident

cerebrovascular accident, multiple

cerebrovascular accident, young adult

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

children

chromosome 19

chronic progressive external ophthalmoplegia

cleft palate

Clinical Pathologic Conference(C.P.C.)

coma

congenital heart disease

congenital malformation

congenital myasthenic syndromes

congenital myopathy

consanguinity

cough

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

cytochrome c oxidase

cytochrome c oxidase, deficiency

deafness

deafness, bilateral progressive vs.unilateral acute

deafness, unilateral

dementia

developmental retardation

diabetes mellitus

diarrhea

diplopia

distal muscle weakness

electrocardiogram, abnormal

electromyogram

encephalopathy

encephalopathy, progressive

exercise intolerance

extraocular muscle lesion

eye movement, disorders of

facial appearance, abnormal

facial nerve palsy

facial nerve palsy, bilateral

facial pain

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

familial

fatigue

fever

fluorescein angiography

gastrointestinal disease, neurologic complications

gastrointestinal motility

genetic diagnosis, prenatal

genetic neurologic disorders

genetic testing

granulomatosis with polyangiitis

granulomatous disease

heralding manifestation

high arched palate

Hirschprung's disease

inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with

intestinal pseudoobstruction

iris, abnormal

isoniazid

jaw pain

Kearns-Sayre syndrome

klippel feil syndrome

Korsakoff's psychosis

lactic acidemia

Leber's hereditary optic neuropathy

Leigh's disease

leukemia, neurologic findings assoc.with

leukodystrophy

leukoencephalopathy

leukopenia

lymphoma involving CNS

lymphomatoid granulomatosis

MELAS syndrome

meningismus

meningoencephalopathy

mental retardation

MERRF syndrome

methotrexate

methylhydrazine derivatives

migraine

misdiagnosis

mitochondrial disease

mitochondrial disease, pathogenesis

mitochondrial encephalomyopathy

MNGIE syndrome

molecular genetics

monoamine oxidase inhibitors

movement disorder

MRI

MRI, abnormal

muscle atrophy, progressive

muscle biopsy

muscle pain

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, cardiovascular changes with

muscular dystrophy, differential diagnosis of

muscular dystrophy, facioscapulohumeral

myasthenia gravis

myasthenia gravis, congenital

myasthenia gravis, differential diagnosis

myasthenia gravis, distal weakness

myasthenia gravis, familial incidence of

myasthenia gravis, limb-girdle

myasthenia gravis, misdiagnosis of

myasthenia gravis, seronegative

myelopathy

myoclonus

myopathy

myopathy, centronuclear

myopathy, mitochondrial

nemaline rod myopathy

nerve conduction studies

neuroendocrinology

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic evaluation

neuromuscular blockade

neuromuscular junction

neuromuscular junction, abnormality of

neuroophthalmology

neuropathy

neuropathy, peripheral

nystagmus, dissociated

nystagmus, vertical

ocular motility, disorders of

ocular myopathy

oculopharyngeal muscular dystrophy

ophthalmoplegia

ophthalmoplegia, progressive external

optic atrophy

optic neuropathy

orthostatic hypotension

Parkinsonism syndrome

percussion induced muscle contraction

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

POLG1 gene

polyneuropathy

pregnancy, neurologic complications in

procarbazine

prognosis

progressive neurologic disorder

prostigmine

pseudomyasthenia

psychiatric problems in neurologic disorders

psychosis

ptosis

ptosis, bilateral

ptosis, classification of

ptosis, familial

ptosis, unilateral

pulmonary infiltrates

sensorineural hearing loss

seronegative

short stature

skin, lesions in neurologic disorders

slit lamp examination

spasticity

spina bifida

splenomegaly

steroid therapy, CNS treatment and complications with

strokelike episodes

syringomyelia

systemic illness

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

testicular atrophy

thrombocytopenia

tinnitus

treatment of neurologic disorder

trinucleotide repeats

upgaze, paralysis of

vertigo

vinblastine

vincristine neurotoxicity

vocal cord paralysis

weakness

weakness, fatiguable

weakness, generalized

weakness, progressive

weaning from respirator, failure to

Wildervanck's syndrome

wrist drop

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