PPT-Myotonic Dystrophy Research: What’s Next

Peg Nopoulos MD 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. 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 . Presented by : . Janel Phetteplace. , . MS. ,. CGC. Janel. -Phetteplace@uiowa.edu. Overview of Genetics. Genes (DNA) Comprise Each Chromosome. . Cell. Chromosome. DNA. DMPK. Gene. . Inheritance. . 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. . therapeutic. . genetic. . sequences. in . muscle. LEONIDAS A. PHYLACTOU. THE CYPRUS INSTITUTE OF NEUROLOGY & GENETICS. Muscular Dystrophy. Group . of muscle diseases . Inherited. Muscle weakness and wasting . 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 . Nicholas Johnson, MD. Assistant Professor of Neurology, Pediatrics, Pathology. University of Utah. Disclosures. Funding/Conflicts of Interest:. NINDS (1K23NS091511-01). Center for Disease Control and Prevention (DD001108-02). 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. 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 ANESTHETIC MANAGEMENT OF A MYOTONIC DYSTROPHY PATIENT Marla Ferschl, MD, Richard Moxley, MD, John W. Day, MD, PhD and Michael Gropper, MD, PhD. Acknowledgement: We gratefully acknowledge Neal Campb A 68yearold female presents with progressive decline in vision and glare Richard C. Allen, MD, PhD August 21, 2013Chief Complaint: Past Ocular History: Ocular Hypertension Past Medical History: Brea What is Myotonic Dystrophy?Myotonic Dystrophy is an inherited neuromuscular condition caused by an abnormality in the DPKM gene, which is located on chromosome 19. The condition is caused by an expan . 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. The Christopher Project. A comprehensive survey of patients and family members/caregivers living with myotonic dystrophy in the U.S.A. and Canada. A collaborative partnership . between patients and families, patient advocacy .