WordNet
- situated farthest from point of attachment or origin, as of a limb or bone
- directed away from the midline or mesial plane of the body
- any degenerative disorder resulting from inadequate or faulty nutrition
PrepTutorEJDIC
- 中心から遠い,末梢(まっしょう)[部]の,末端[部]の
- 栄養障害 / 筋萎縮症,筋ジストロフィー(筋肉の退化・萎縮・運動障害などが起こる病気)
UpToDate Contents
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English Journal
- Distal muscular dystrophies.
- Udd B1.
- Handbook of clinical neurology.Handb Clin Neurol.2011;101:239-62. doi: 10.1016/B978-0-08-045031-5.00016-5.
- Distal muscular dystrophies are a group of inherited primary muscle disorders showing progressive weakness and atrophy preferentially in the hands, forearm, lower legs, or feet. Extensive progress in understanding the molecular genetic background has changed the classification and extended the list
- PMID 21496636
- Muscle magnetic resonance imaging shows distinct diagnostic patterns in Welander and tibial muscular dystrophy.
- Mahjneh I1, Lamminen AE, Udd B, Paetau AE, Hackman P, Korhola OA, Somer HV.
- Acta neurologica Scandinavica.Acta Neurol Scand.2004 Aug;110(2):87-93.
- OBJECTIVES: This is a report on a retrospective muscle magnetic resonance imaging (MRI) study on 11 patients affected by Welander distal myopathy (WDM) and 22 patients with tibial muscular dystrophy (TMD) carried out in order to define the pattern and characteristics of muscle involvement.RESULTS: W
- PMID 15242415
Related Links
- Welander distal muscular dystrophy symptoms, causes, diagnosis, and treatment information for Welander distal muscular dystrophy (Welander distal myopathy, Swedish type) with alternative diagnoses, full-text book chapters ...
- Clinical Synopsis TEXT A number sign (#) is used with this entry because Welander distal myopathy (WDM) is caused by heterozygous mutation in the TIA1 gene (603518) on chromosome 2p13. Some patients may have a ...
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- 関
- centrifugal、distalis、distally、distant、efferent、end、extremity、terminal、terminally
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- (医)栄養失調、栄養失調症。(医)異栄養、異栄養症、ジフトロフィー
- 栄養障害。細胞や組織の物質代謝障害によって変性・萎縮などの起こること。