Your browser doesn't support javascript.
loading
Montrer: 20 | 50 | 100
Résultats 1 - 2 de 2
Filtre
1.
Journal of the Korean Neurological Association ; : 345-351, 2004.
Article Dans Coréen | WPRIM | ID: wpr-213984

Résumé

BACKGROUND: Hereditary neuropathy with liability to pressure palsy (HNPP) and Charcot-Marie-Tooth1A (CMT1A) are autosomal dominant inherited demyelinating neuropathy associated with the deletion or duplication of 17p11.2-p12 segments including the gene for peripheral myelin protein 22 (PMP22). The aim of this study is to compare the electrophysiological features of these two disorders genetically related. METHODS: We studied the nerve conduction studies of genetically confirmed 43 HNPP in 23 families and 31 CMT1A patients in 13 families. RESULTS: Nerve conduction studies presented prolonged terminal latency, slow nerve conduction velocity and low amplitude of compound muscle or nerve action potentials in both diseases, but more severe in CMT1A. The incidence of conduction block with or without dispersion was higher in CMT1A than HNPP, with 23.6% and 5.7% respectively. CMT1A revealed a rather even distribution of abnormalities in segmental nerve conduction studies than HNPP. HNPP showed frequent involvements at the segment of entrapment-prone site such as peroneal and ulnar nerves. The characteristical differences of these diseases could be defined by the quantitative correlation study. The correlation coefficients of nerve conduction velocities between tested nerves in the same or different limbs and between tested segments of the same nerve was much higher in CMT1A than HNPP. CONCLUSIONS: We conclude that CMT1A presents with more severe diffuse and uniform slowing, whereas HNPP presents with focal electrophysiological abnormalities.


Sujets)
Humains , Potentiels d'action , Membres , Incidence , Gaine de myéline , Conduction nerveuse , Paralysie , Statistiques comme sujet , Nerf ulnaire
2.
Journal of the Korean Neurological Association ; : 300-303, 2003.
Article Dans Coréen | WPRIM | ID: wpr-69033

Résumé

CNS infection due to Listeria monocytogenes is a rare condition that occurs primarily in immunocompromised patients. A predilection for the brainstem has been proposed but definite abscess formation is extremely rare. We report a case of necrotizing meningoencephalitis with diffuse extensive abscesses caused by Listeria monocytogenes in a chronic diabetic patient, whose diagnosis was based on blood culture and MRI findings.


Sujets)
Humains , Abcès , Abcès cérébral , Tronc cérébral , Encéphale , Diagnostic , Sujet immunodéprimé , Listeria monocytogenes , Listeria , Imagerie par résonance magnétique , Méningoencéphalite
SÉLECTION CITATIONS
Détails de la recherche