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CHARCOT-MARIE-TOOTH DISEASE IN NORTHERN SWEDEN - AN EPIDEMIOLOGIC AND CLINICAL-STUDY
Author(s): HOLMBERG BH
Source: ACTA NEUROLOGICA SCANDINAVICA    Volume: 87    Issue: 5    Pages: 416-422    Published: MAY 1993  
Times Cited: 16     References: 34     
Abstract: One hundred four cases of Charcot-Marie-Tooth disease (CMT) in 52 families were identified within a defined area in northern Sweden corresponding to a prevalence rate of 20.1 cases per 100000 (Dec 31 1991) for all subtypes. The prevalence of CMT type I was 16.2 per 100000. The distribution of cases was not uniform. The prevalence rate is compared with previous prevalence studies focusing on Charcot-Marie-Tooth disease or hereditary motor and sensory neuropathy (HMSN). Three patients were classified as the distal spinal muscular atrophy type of CMT and one patient was not possible to classify. For seventy-five patients, available to clinical examination within the study, data were collected as to age at onset, symptoms, clinical findings and degree of disability.
Document Type: Article
Language: English
Reprint Address: HOLMBERG, BH (reprint author), HARNOSANDS SJUKHUS, DEPT INTERNAL MED, S-87129 HARNOSAND, SWEDEN
Addresses:
1. UMEA UNIV HOSP, DEPT NEUROL, S-90185 UMEA, SWEDEN
Publisher: MUNKSGAARD INT PUBL LTD, 35 NORRE SOGADE, PO BOX 2148, DK-1016 COPENHAGEN, DENMARK
Subject Category: Clinical Neurology
IDS Number: LF798
ISSN: 0001-6314
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