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✔️ 標題 : The Road to Edmond
✔️ 片長 :125 Minutes
✔️ 类型:
✔️ 語言 :粵語 (中文字幕)
✔️ 視頻解析度: 720p-1080p HD
✔️ 視頻格式 : mp4
✔️ 上映日期: 2018-07-29
✔️ 演員 : / 更多...
劇情簡介:
Synopsis :
Emery Dreifuss Muscular Dystrophy NORD National ~ EmeryDreifuss muscular dystrophy EDMD is a rare often slowly progressive genetic disorder affecting the muscles of the arms legs face neck spine and heart The disorder consists of the clinical triad of weakness and degeneration atrophy of certain muscles joints that are fixed in a flexed
Cardiac features of Emery–Dreifuss muscular dystrophy ~ Emery–Dreifuss muscular dystrophy EDMD is a genetic disorder characterized by early onset contractures of the elbows Achilles tendons and postcervical muscles with progressive muscle wasting and weakness α helical rod EDMD in five of 17 cases
EmeryDreifuss Muscular Dystrophy EDMD Muscular ~ What is EmeryDreifuss muscular dystrophy EmeryDreifuss muscular dystrophy EDMD is one of nine types of muscular dystrophy a group of genetic degenerative diseases primarily affecting voluntary muscles It is named for Alan Emery and Fritz Dreifuss physicians who first described the disorder among a Virginia family in the 1960s
Autosomal dominant Emery–Dreifuss dystrophy due to ~ Background Autosomal dominant Emery–Dreifuss muscular dystrophy EDMDAD is a disorder characterized clinically by humeropelvic weakness contractures and cardiomyopathy and genetically by mutations in the lamin AC gene on 1q212q213 Of the 14 lamin AC gene mutations reported thus far the four involving the rod domain have been associated with isolated cardiomyopathy and conduction
EmeryDreifuss Muscular Dystrophy Treatment Management ~ Although it was probably first described in the early 1900s EmeryDreifuss muscular dystrophy EDMD was not clearly delineated as a separate disease until the 1960s In 1961 Dreifuss and Hogan described a large family with an Xlinked form of muscular dystrophy that they considered to be a benign form of Duchenne muscular dystrophy
EmeryDreifuss Muscular Dystrophy Background ~ Although it was probably first described in the early 1900s EmeryDreifuss muscular dystrophy EDMD was not clearly delineated as a separate disease until the 1960s In 1961 Dreifuss and Hogan described a large family with an Xlinked form of muscular dystrophy that they considered to be a benign form of Duchenne muscular dystrophy
EmeryDreifuss muscular dystrophy European Journal of ~ EmeryDreifuss muscular dystrophy EDMD is a relatively benign form of dystrophy with onset in early childhood and thereafter relatively slow progression that is characterised by the triad 1 1
EmeryDreifuss Muscular Dystrophy an overview ~ EmeryDreifuss Muscular Dystrophy EmeryDreifuss muscular dystrophy EDMD is related to loss of the nuclear membrane protein emerin in Xlinked XL inheritance in the STA gene and loss of lamin AC in autosomal dominant AD inheritance In XLEDMD muscle disease is milder and progresses more slowly than in ADEDMD
UpToDate ~ EmeryDreifuss muscular dystrophy EDMD also known as humeroperoneal muscular dystrophy can be inherited as an Xlinked recessive autosomal dominant or autosomal recessive disorder The pathogenesis genetics and clinical characteristics of EDMD are discussed here
Autosomal dominant EmeryDreifuss dystrophy due to ~ Of the 14 lamin AC gene mutations reported thus far the four involving the rod domain have been associated with isolated cardiomyopathy and conductionsystem disease This is the first report of rod domain mutations in patients with the full EDMDAD phenotype METHODSClinical pathologic and genetic data are provided on two families with
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