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ion on which the epithelial cells which turn causes recurrent epithelial erosions in which the epitheliums outermost layer rises slightly exposing a small gap between the oute Symptoms urred vi. Jinghua. Chen, MD, PhD. University of Louisville. Department of Ophthalmology and Visual Sciences. April 3, 2015. History. CC:. Progressive decreased central vision OU for one year.. HPI. : . 27 . but can occasionally be severe and disabling, many years after the first onset of symptoms. Facial weakness may develop, and be commented upon by the specialist,but rarely causes any particular proble Muscular Dystrophy. 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. Presented by:. Sujitha B Subramaniam. 11408044. IV yr Genetic Engineering. SRM University. DUCHENNE MUSCULAR DYSTROPHY.  (. DMD. ) is a recessive X-linked form of muscular dystrophy, which results in muscle degeneration, difficulty . 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. S H Subramony M.D.. Professor of Neurology and Pediatrics, . University of Florida and McKnight Brain Institute. Center for . Neurogenetics. SOME OF THE UF MYOTONIC DYSTROPHY TEAM. Andy Berglund, John Williamson, William Miles, George . Glen Nuckolls, PhD. Program Director, Neurogenetics Cluster. Division of Extramural Research. National Institute of Neurological Disorders and Stroke. g. len.nuckolls@nih.gov. NIH . Bethesda Campus . Ali Al Khader, M.D.. Faculty of Medicine. Al-Balqa’ Applied University. Email: ali.alkhader@bau.edu.jo. Lecture outline. Skeletal muscle atrophy. Inflammatory myopathies:. - . D. ermatomyositis. Polymyositis. 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. 10/15/2019 1 Easy to diagnose but hard to remember Dr. Mohamed Abdelmoniem Mohamed Sedik Ophthalmology resident, MIOR 1. Bilateral. 2. Symmetrical. 3. Inherited condition. 4. Little or no relationsh 10 Volume 18, Issue 5 9 Groznova O.S., Artemeva S.B. Porazhenie serdechno-sosudistoy sistemyi pri progressiruyuschey myishechnoy distro�i Rossiyskiy vestnik perinatologii i pediatrii. 2013; Heart involvement in Myotonic Dystrophy is one of the most important aspects of the condition because of its potentially serious consequences. Many cardiac complications can be treated if detected ear . Villacrés. Carlos . Carlosama. Signs. and . symptoms. Progressive muscular wasting. Poor balance. Drooping eyelids. Atrophy. . Scoliosis.  (curvature of the spine and the back). Inability to walk.