Your browser doesn't support javascript.
loading
A Clinical Profile of Peripheral Neuropathy in Korean Children / 대한소아신경학회지
Article de Ko | WPRIM | ID: wpr-99563
Bibliothèque responsable: WPRO
ABSTRACT
PURPOSE: To analyze the clinical features of peripheral neuropathy in Korean children. METHODS: A total of 62 children with acute flaccid paralysis, longstanding weakness of extremities, or abnormal electrophysiological studies, suggestive of peripheral neuropathy, were evaluated retrospectively from the hospital records. The subjects were recruited at the pediatric neurology and endocrine clinic, Kyungpook National University Hospital from 2000 to 2002 and they all went through neurological examination and electrophysiological studies with or without nerve biopsy. RESULTS: Thirty nine children(Male 24:Female 15; Mean age 7.6+/-4.3 years) were found to have clinical peripheral neuropathy. Inflammatory neuropathy(5 children with Guillain Barre syndrome, 1 children with chronic inflammatory demyelinating polyneuropathy, 12 children with Bell's palsy; 46%) was the most common, followed by hereditary neuropathy(4 children, 10%), Chemotherapy induced neuropathy(3 children, 8%), metachromatic leukodystrophy(2 children, 5%), trauma(2 children, 5%), diabetic neuropathy(1 children, 3%) and so on. Thirty two children had motor neuropathy(82%), six children had combined motor and sensory neuropathy(15%), two had pure sensory(5%), but nobody had autonomic neuropathy. With respect to the type of involvement, polyneuropathies constitute 59%(23 children), mononeuropathy simplex accounted for 38%(15 children), mononeuropathy multiplex was found in 3%(1 child). Based on electrophysiological studies and biopsy results, demyelinating neuropathy was seen in 22 children(56%), axonal neuropathy in 12 children(31%), combined neuropathy in 5 children(13%). Eighteen children(46%) were completely or almost completely recovered from the illness. CONCLUSION: Inflammatory neuropathy was the most common among the acquired neuropathies and hereditary motor sensory neuropathy was the most common among the genetic neuropathies. Treatable neuropathies took up 46%. Potentially preventable neuropathies accounted for 36%. Early diagnosis and early intervention may have significant impacts on the prognosis of peripheral neuropathy in children.
Sujet(s)
Mots clés
Texte intégral: 1 Indice: WPRIM Sujet Principal: Paralysie / Polyneuropathies / Pronostic / Axones / Biopsie / Archives administratives hospitalières / Études rétrospectives / Neuropathies périphériques / 32270 / Paralysie faciale de Bell Type d'étude: Diagnostic_studies / Observational_studies / Prognostic_studies / Screening_studies Limites du sujet: Child / Humans langue: Ko Texte intégral: Journal of the Korean Child Neurology Society Année: 2003 Type: Article
Texte intégral: 1 Indice: WPRIM Sujet Principal: Paralysie / Polyneuropathies / Pronostic / Axones / Biopsie / Archives administratives hospitalières / Études rétrospectives / Neuropathies périphériques / 32270 / Paralysie faciale de Bell Type d'étude: Diagnostic_studies / Observational_studies / Prognostic_studies / Screening_studies Limites du sujet: Child / Humans langue: Ko Texte intégral: Journal of the Korean Child Neurology Society Année: 2003 Type: Article