PPT-The Role of Rehab for Myotonic Dystrophy

Lisa Warren MHS OTRL UF Health Rehab ClientCentered Approach Multidisciplinary approach Healthcare professionals working together for the common goal of improving the patients health function and quality of life. What it is…. Muscular Dystrophy is a family of hereditary disease that cause progressive and steady muscle weakening.. Duchenne. and Becker muscular dystrophy, (which are just 2 forms of MD) alone affect approximately 1 in every 3,500 to 5,000 boys.. Nicholas Johnson, MD . Assistant Professor of Neurology, Pediatrics, Pathology. University of Utah. On behalf of: JD Franklin, E Nasser, E . Luebbe. , J Hilbert, KA Hagerman, JW Day, E . Ciafaloni. , M Hung, CR . & Myotonic Dystrophy. Presented by : . Janel Phetteplace. , . MS. ,. CGC. Janel. -Phetteplace@uiowa.edu. Overview of Genetics. Genes (DNA) Comprise Each Chromosome. . Cell. Chromosome. DNA. DMPK. Sherri Garcia. Muscular Dystrophy: Walk a Mile in Their Shoes. CDC’s 2005 Science Ambassador Program. Overview. Sympathy vs. empathy. Basic information about Duchenne muscular dystrophy. Inheritance. Peg Nopoulos, M.D. Professor of Psychiatry. Ian DeVolder, PhD, MDF Postdoctoral Fellow. Research In Myotonic Dystrophy (DM). Types of Human Research Studies. Should I volunteer for a research study?. Anesthetic Management of a Myotonic Dystrophy PatientMyotonic Dystrophy Foundationwwwmyotonicorg1Practical Suggestions for the Anesthetic Management of a Myotonic Dystrophy PatientOverviewRisks of ane Division of Pulmonary Critical Care and Sleep. Medical Director KU Sleep Laboratory. KUMC Myotonic Dystrophy Day. Pulmonary Treatments. July 20, 2019. Respiratory and Sleep Issues in Myotonic Dystrophy. Mark Hamilton, . (formerly) Clinical . Research Fellow . West of Scotland Clinical Genetics Service. markhamilton1@nhs.net. Scottish management guidelines for myotonic dystrophy. www.smn.scot.nhs.uk. ________________________________ Hamilton Health Sciences, 2008PD 6204 1/2004dpc/pted/FSHlw.docdt/January 30, 2014 Facioscapulohumeral Muscular Dystrophy What is Facioscapulohumeral Muscular Dys The Character and Frequency of Muscular Pain in Myotonic Dystrophy and Their Relationship to Myotonia Myotonic dystrophy is the most common form of International Journal ofNeurology and Neurotherapy August 2000The development and printing of this booklet was funded by theNational Institute on Disability and Rehabilitation Research, adivision of the U. S. Department of Education, Grant #H133B98000 TIG 41/08 Updated : July 2018 R eview: Date July 2020 Page 1 of 4 S ain t Mary’s Hospital Manchester Centre for Genomic Medicine Information for Patients Myotonic Dystrophy Myotonic dystrophy has S H Subramony M.D.. Professor of Neurology and Pediatrics. University of Florida College of Medicine. Steinert H (1909) Über das klinische und anatomische Bild des Muskelschwunds der Myotoniker. Dtsch Z Nervenheilkd 37:58–104. is a muscle disease unrelated to any disorder of innervation or neuromuscular junction. . These . conditions have widely varying etiologies, including congenital or inherited, idiopathic, infectious, metabolic, inflammatory, endocrine, and drug-induced or .