Intraoperative Electrophysiological Monitoring during Microvascular Decompression for Hemifacial Spasm and Surgical Outcome
Journal of the Korean Neurological Association
;
: 260-265, 2001.
Article
in Korean
| WPRIM
| ID: wpr-87682
ABSTRACT
BACKGROUND:
Hereditary neuropathy with liability to pressure palsies (HNPP) is a peripheral nerve disorder characterized by autosomal dominant inheritance, recurrent pressure palsies, reduced motor and sensory conduction velocities and sausage-like swellings (tomacula) of myelin sheaths in nerve biopsy. A 1.5-Mb deletion in chromosome 17p11.2- p12 is present in the majority but not all cases of HNPP. The aim of the present study was to evaluate the clinical, electrophysiological and morphological aspects of HNPP patients associated with chromosome 17p11.2-p12 deletion.METHODS:
To detect the presence of the deletion, the DNA of the patients was analyzed with pVAW409R3 (D17S122). An electrophysiological study was done in all patients. Sural nerve biopsy with teasing was done in three patients.RESULTS:
DNA analysis and electrophysiological tests revealed the deletion in 8 families and 16 patients. Nerve conduction studies demonstrated diffuse mild to moderate slowing of nerve conduction velocities especially worse over the common entrapment sites, regardless of clinical manifestations. The long duration of compound muscle and nerve action potentials without conduction blocks or dispersion is characteristic of patients with HNPP. The tomacula of myelin sheaths was found on sural nerve teasing.CONCLUSIONS:
We report the clinical, electrophysiological and morphological aspects of the Korean HNPP patients associated with chromosome 17p11.2-p12 deletion. (J Korean Neurol Assoc 19(3)251~259, 2001)
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Paralysis
/
Peripheral Nerves
/
Sural Nerve
/
Wills
/
Biopsy
/
Action Potentials
/
DNA
/
Hemifacial Spasm
/
Microvascular Decompression Surgery
/
Myelin Sheath
Limits:
Humans
Language:
Korean
Journal:
Journal of the Korean Neurological Association
Year:
2001
Type:
Article
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