Medical dictionary. 2011.
Welander distal myopathy (myopathy) — We·lan·der distal myopathy (myopathy) (vaґlahn dər) [Lisa Welander, Swedish neurologist, 1909–2001] see under myopathy … Medical dictionary
late distal hereditary myopathy — Welander distal m … Medical dictionary
distal myopathy — any of numerous forms of muscular dystrophy, varying in mode of inheritance and age of onset, that affect first the feet and hands and progress to involve more proximal muscle groups. Among the disorders included here are Welander distal m. and… … Medical dictionary
Distal muscular dystrophy — Classification and external resources ICD 10 G71.0 ICD 9 359.1 … Wikipedia
Disease — Illness or sickness often characterized by typical patient problems (symptoms) and physical findings (signs). Disruption sequence: The events that occur when a fetus that is developing normally is subjected to a destructive agent such as the… … Medical dictionary
Dysferlin — Dysferlin, limb girdle muscular dystrophy 2B (autosomal recessive) Identifiers Symbols DYSF; FER1L1; FLJ00175; FLJ90168; LGMD2B External IDs … Wikipedia
List of neurological disorders — This is a list of major and frequently observed neurological disorders (e.g., Alzheimer s disease), symptoms (e.g., back pain), signs (e.g., aphasia) and syndromes (e.g., Aicardi syndrome). Contents: Top · 0–9 A B C D E F G H I J K L M N O P … Wikipedia
Muskeldystrophie — Muskeldystrophien, auch progressive Muskeldystrophie (Dystrophia musculorum progressiva), sind eine Gruppe von Muskelerkrankungen. Es handelt sich um Erbkrankheiten, die durch Mutationen im Erbgut verursacht werden, welche meist zu Defekten oder… … Deutsch Wikipedia
List of diseases (W) — A list of diseases in the English wikipedia.DiseasesTOC W* W syndromeWaWaa Wan* Waaler Aarskog syndrome * Waardenburg syndrome type 1 * Waardenburg syndrome type 2 * Waardenburg syndrome type 2A * Waardenburg syndrome type 2B * Waardenburg… … Wikipedia
Werdnig-Hoffmann disease — Werd·nig Hoff·mann disease vert nik hof .män n atrophy of muscles that is caused by degeneration of the ventral horn cells of the spinal cord, is inherited as an autosomal recessive trait, becomes symptomatic during early infancy, is… … Medical dictionary
