Results 281 to 290 of about 108,126 (340)

Cranial nerve involvement in Charcot–Marie–Tooth Disease

open access: closedJournal of Clinical Neuroscience, 2017
Charcot-Marie-Tooth Disease (CMT) is a rare disorder with less than 200,000 cases reported in the US every year, making diagnosis challenging. MR and CT imaging has become more common in the evaluation of CMT to identify areas of disease involvement.A 27-year-old female from Guatemala with a past history of polio initially presented to the emergency ...
Nirav Das   +3 more
openaire   +3 more sources

CRANIAL NERVE DISEASE

open access: closedInternational Ophthalmology Clinics, 1967
William S. Joffe
openaire   +3 more sources

Multiple cranial nerve enlargement in Charcot-Marie-Tooth disease

Journal of Neurology, Neurosurgery & Psychiatry, 2020
Hypertrophy of peripheral nerves are commonly reported in patients with demyelinating forms of Charcot-Marie-Tooth disease (CMT).1 Herein, an under-recognised association with hypertrophy of multiple cranial nerves in a patient with CMT is described. A 39-year-old otherwise healthy man presented with a 2-month history of tension-type headaches without
William Huynh, Lynette Masters
openaire   +2 more sources

Diseases of the Eighth Cranial Nerve

open access: closed, 2005
DORIS-EVA BAMIOU, LINDA M. LUXON
openaire   +2 more sources

Cerebrovascular Brainstem Diseases with Isolated Cranial Nerve Palsies

Cerebrovascular Diseases, 2002
There is a significant number of individual patients with cranial nerve palsies as the sole manifestation of MRI- and, less frequently, CT-documented small brainstem infarctions or hemorrhages. The 3rd and 6th nerves are most commonly involved and, less frequently, the 4th, 5th, 7th, and 8th nerves.
Frank, Thömke   +3 more
openaire   +2 more sources

Multiple cranial nerve enhancement in early infantile Krabbe’s disease

Neurology, 2000
Krabbe’s disease or globoid-cell leukodystrophy is an autosomal recessive disorder caused by a mutation of the galactocerebroside beta-galactosidase gene located at chromosome 14q31.1 The reduction of enzymatic activity affects the catabolism of galactosylceramide to ceramide and galactose.1 This disorder is characterized by an abnormal breakdown and ...
O G, Bernal, N, Lenn
openaire   +2 more sources

Lyme Disease Presenting with Gastroparesis and Cranial Nerve Vii Palsy

open access: closedAmerican Journal of Gastroenterology, 2008
Bryan Kavanaugh   +2 more
openaire   +2 more sources

Self-Limiting Fourth and Sixth Cranial Nerve Palsy After Lyme Disease

Journal of Pediatric Ophthalmology & Strabismus, 2010
Lyme disease, or borreliosis, is caused by a bacteria ( Borrelia burgdorferi sensu lato) and is transmitted to humans by the bite of ticks of the Ixodes genus. The authors describe a 16-year-old girl who presented with extraocular muscle palsies and had serology positive for Lyme disease. The
Vinod, Sharma, Susmito, Biswas
openaire   +2 more sources

Monoparesis (monoplegia) and cranial mononeuropathy. Peripheral/cranial nerve and nerve root diseases.

Problems in veterinary medicine, 1992
Monoparesis (monoplegia) refers to partial (monoparesis) or complete (monoplegia) loss of voluntary motor function in a single limb. Cranial mononeuropathy implies that there is dysfunction referable to a single cranial nerve. These neurologic problems are generally associated with peripheral and cranial nerve lesions, respectively.
openaire   +1 more source

[Kawasaki disease and cranial nerve involvement: two cases].

Archives de pediatrie : organe officiel de la Societe francaise de pediatrie, 2016
CNS involvement, except classical lymphocytic meningitis, is exceptionally rare in Kawasaki disease. Herein, we report on two atypical cases of KD with cranial nerve inflammation. The first case presented supranuclear vertical palsy and the second case Bell palsy.
M-C, Delafay   +5 more
openaire   +1 more source

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