81. Gale Encyclopedia Of Medicine Myotonic Dystrophy myotonic dystrophy. myotonic dystrophy is a progressive disease that keeps affected muscles from relaxing once they have been contracted or tightened. http://www.findarticles.com/cf_dls/g2601/0009/2601000942/p1/article.jhtml

@import url(/css/us/style.css); @import url(/css/us/searchResult1.css); @import url(/css/us/articles.css); Advanced Search Home Help IN all publications this publication Automotive Business Computing Entertainment Health News Reference Sports YOU ARE HERE Articles Content provided in partnership with Print friendly Tell a friend Find subscription deals Myotonic dystrophy by Richard Robinson Definition Myotonic dystrophy is a progressive disease that keeps affected muscles from relaxing once they have been contracted or tightened. Description Myotonic dystrophy (DM), also called dystrophia myotonica, myotonia atrophica, or Steinert's disease, is a common form of muscular dystrophy. It affects more than 30,000 people in the United States. DM is an inherited disease, affecting men and women approximately equally. Symptoms may appear at any time from childhood to adulthood. DM causes general weakness, usually beginning in the muscles of the hands, feet, neck, or face. It slowly progresses to involve other muscle groups, including the heart. DM affects a wide variety of other organ systems as well. A rare form of DM, congenital myotonic dystrophy, may appear in newborns of mothers who have DM. Congenital myotonic dystrophy is marked by severe weakness, poor sucking and swallowing responses, respiratory difficulty, delayed motor development, and mental retardation.

82. Autosomal Dominant: Myotonic Dystrophy Autosomal Dominant myotonic dystrophy. Genes are inherited from our biological parents in specific ways. What is myotonic dystrophy? http://www.stlouischildrens.org/articles/content.asp?pageid=P02112

83. Gene Link Catalog Ordering System GeneProber™ Genemer™ Fragile X Syndrome Huntington Disease myotonic dystrophy Friedreich s Ataxia Sickle Cell Sry, X Y Rh Species Genetic Identity http://www.genelink.com/geneprodsite/category.asp?c=91

84. Neurology -- Abstracts: Day Et Al. 60 (4): 657 Neurology 2003;60657664 © 2003 American Academy of Neurology myotonic dystrophy type 2. Molecular, diagnostic and clinical spectrum. http://www.neurology.org/cgi/content/abstract/60/4/657

HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: Figures Only for this Article Full Text of this Article PDF Version of this Article CME: Take the quiz for this article Data Supplement Citation Map Email this article to a friend Correspondence: Submit a response to this article Similar articles found in: Neurology Online PubMed PubMed Citation This Article has been cited by: other online articles Search PubMed for articles by: Day, J. W. Ranum, L. P.W. Alert me when: new articles cite this article Download to Citation Manager Collections under which this article appears: All Neuromuscular Disease Muscle disease All Genetics Trinucleotide repeat diseases Neurology American Academy of Neurology Myotonic dystrophy type 2 Molecular, diagnostic and clinical spectrum J. W. Day, MD PhD K. Ricker, MD J. F. Jacobsen, BS L. J. Rasmussen, BA K. A. Dick, BA W. Kress, PhD C. Schneider, MD M. C. Koch, MD G. J. Beilman, MD A. R. Harrison, MD J. C. Dalton, MS and L. P.W. Ranum, PhD Address correspondence and reprint requests to Dr. John W. Day, Department of Neurology and Institute of Human Genetics, MMC 206, University of Minnesota School of Medicine, 420 Delaware St. SE, Minneapolis, MN 55455; e-mail:

85. Remifentanyl In Myotonic Dystrophy Remifentanil in myotonic dystrophy – Avoiding the Use of Muscle Relaxants and Long Acting Opioids. Dr. Karen Grimsehl, MBChB, FRCA http://www.uam.es/departamentos/medicina/anesnet/journals/ija/vol4n2/remi.htm

Dr. Karen Grimsehl, MBChB, FRCA Specialist Registrar in Anesthetics Tayside University Hospital Dr.Edward Wilson, MBChB, FFARCSI Consultant in Anesthetics and Intensive Care Tayside University Hospitals The correct citation of this article for reference is: http://www.ispub.com/journals/IJA/Vol4N1/remi.htm ; Published April 1, 2000; Last Updated April 1, 2000. (Please add the "Date accessed") Quick Links Abstract Introduction Case Report Discussion ... References Abstract Myotonic dystrophy, a genetic disorder of abnormal musle function, is associated with many anesthetic hazards. Sensitivity to anesthetic drugs, especially muscle relaxants and opioids, may complicate postoperative care. A period of postoperative ventilation to allow opioids and sedatives to wear off may be required. The use of succinylcholine is contra-indicated because of profound muscle contraction which can make ventilation impossible. Non-depolarising agents can also give unpredictable responses, ranging from decreased sensitivity to exaggerated response. We describe a case where the use of remifentanil allowed ventilation of a patient with myotonic dystrophy for more than 2 hours and avoided the use of muscle relaxants and longer acting opioids. The short context-sensitive half-time of remifentanil allowed immediate recovery and safe discharge home on the same day. Key words: remifentanil, myotonia, myotonic dystrophy, anesthesia

86. Myotonic Dystrophy - DNA Analysis myotonic dystrophy, DNA Analysis, MDY, DM1. myotonic dystrophy is a understanding of these phenomena . myotonic dystrophy DNA ANALYSIS. http://www.bcmgeneticlabs.org/tests/dna/myotonicdystrophy.html

MYOTONIC DYSTROPHY DNA ANALYSIS Open Page in New Window Print This Page Return to Search Reasons for Referral: Confirmation of diagnosis of affected individual Carrier identification Prenatal diagnosis Testing Methodology: Direct Mutation Analysis: PCR analysis across the CTG repeat region to determine allele size(s). This assay is particularly sensitive for identifying alleles between 30-80 repeats. Southern analysis: The MDY1 probe from the myotonin protein kinase gene is used to identify large expansions of the CTG repeat region with Nco I or BamHI digested DNA. Specimen Requirements: Blood: EDTA (purple-top) tubes: Adults: Child: 6 cc; Infant: Requisition form must accompany specimen. For presymptomatic testing, a consent form is required and we recommend that the subject receive genetic counseling. For information about prenatal testing, contact our laboratory. Turnaround Time: 2-3 weeks CPT Codes and Prices Forms: DNA Requisition Shipping Information Prenatal Requisition

87. :: Ez2Find :: Myotonic Dystrophy Guide myotonic dystrophy, Global Metasearch Any Language Guides, myotonic dystrophy. ez2Find Home Directory Health http://ez2find.com/cgi-bin/directory/meta/search.pl/Health/Conditions_and_Diseas

Guide : Myotonic Dystrophy Global Metasearch Any Language English Afrikaans Arabic Bahasa Melayu Belarusian Bulgarian Catala Chinese Simplified Chinese Traditional Cymraeg Czech Dansk Deutsch Eesti Espanol Euskara Faroese Francais Frysk Galego Greek Hebrew Hrvatski Indonesia Islenska Italiano Japanese Korean Latvian Lietuviu Lingua Latina Magyar Netherlands Norsk Polska Portugues Romana Russian Shqip Slovensko Slovensky Srpski Suomi Svenska Thai Turkce Ukrainian Vietnamese Mode All Words Any Word Phrase Results Timeout Depth Adult Filter Add to Favorites Other Search Web News Newsgroups Images Guides Myotonic Dystrophy ez2Find Home Directory Health Conditions and Diseases ... Muscle Diseases : Myotonic Dystrophy Related Categories Health: Conditions and Diseases: Genetic Disorders Health: Conditions and Diseases: Neurological Disorders: Muscle Diseases: Muscular Dystrophies Health: Conditions and Diseases: Rare Disorders Web Sites The CaF Directory [Site Info] [Translate] [Open New Window] An article about myotonic dystrophy, its characteristics and inheritance patterns. URL: http://www.cafamily.org.uk/Direct/m57.html

88. Congenital Myotonic Dystrophy congenital myotonic dystrophy by chickpeas chickpeas@EMAIL PROTECTED Nov 12, 2003 at 1030 PM I have a two month old son http://www.talkaboutsupport.com/group/alt.support.musc-dystrophy/messages/3522.h

Other Recommended Forums: Cooking Health Recovery Romance ... Muscular Dystrophy congenital myot... Post 1 of 1 Topic 21 of 38 congenital myotonic dystrophy by "chickpeas" <chickpeas@[EMAIL PROTECTED] > Nov 12, 2003 at 10:30 PM I have a two month old son diagnosed with congenital myotonic dystrophy. Anyone have any insight with respect to prognosis or similar experience Thanks, chickpeas Post 1 of 1 Topic 21 of 38 1 Posts in Topic: congenital myotonic dystrophy "chickpeas" < Post A Reply: About Advertising Contact Frequently Asked Questions ... Signup Wed Jun 2 20:04:29 EDT 2004.

89. OUP: Myotonic Dystrophy: Harper myotonic dystrophy The Facts. Peter S Harper, Department myotonic dystrophy is part of the group of muscular dystrophies. It is the commonest http://www.oup.co.uk/isbn/0-19-852586-9

VIEW BASKET Quick Links About OUP Career Opportunities Contacts Need help? oup.com Search the Catalogue Site Index American National Biography Booksellers' Information Service Children's Fiction and Poetry Children's Reference Dictionaries Dictionary of National Biography Digital Reference English Language Teaching Higher Education Textbooks Humanities International Education Unit Journals Law Medicine Music Oxford English Dictionary Reference Rights and Permissions Science School Books Social Sciences World's Classics UK and Europe Book Catalogue Help with online ordering How to order Postage Returns policy ... Table of contents Myotonic Dystrophy - The Facts Peter S Harper , Department of Medical Genetics, University of Wales College of Medicine Publication date: 27 June 2002 126 pages, 2 figures and numerous tables, 196mm x 129mm Series: The Facts Search for titles in the same series Ordering Individual customers order by phone, post, or fax Teachers in UK and European schools (and FE colleges in the UK): order by phone, post, or fax A sample of this book is available in PDF format. The first ever popular book on the commonest inherited muscular dystrophy Written clearly and simply for those with no medical expertise Provides essential information on genetic testing, and how to make the difficult decisions.

90. Myotonic Dystrophy Subject myotonic dystrophy Topic Area Neurology General Forum The Neurology and Neurosurgery Forum Question Posted By Lozzer on Thursday, April 11, 2002 http://www.medhelp.org/forums/neuro/messages/31729a.html

Questions in The Neurology Forum are being answered by doctors from The Cleveland Clinic , consistently ranked one of the best hospitals in America. Subject: Myotonic Dystrophy Topic Area: Neurology - General Forum: The Neurology and Neurosurgery Forum Question Posted By: Lozzer on Thursday, April 11, 2002 Having recently been diagnosed with Myotonic dystrophy it has made me more aware of every slight dicomfort, irregularity in my body and worrying whether it has any direct relationship to the disease. I am due to go to see an eye specialist as my neurologist believes there is a problem with my eyes. Now I am worrying about this and would like to know two things really. Firstly what are the likely things that could be wrong with my eyes? and secondly I am a very keen soccer player i play two three times a week, am i likely to be affected by the disease with my playing, i.e will i not be able to play soon etc? would appreciate any help as it can be quite confusing and daunting, i am only 23 and this has come as a massive blow to my self esteem and well being. thanks for your time Lawrence Answer Posted By: CCF-Neuro-M.D.-JT on Wednesday, April 17, 2002

91. Re: Myotonic Dystrophy And Tegretol Subject Re myotonic dystrophy and tegretol Forum The Neurology and Neurosurgery Forum Topic Area Neurology General Posted by CCF MD GS on August 29, 1998 http://www.medhelp.org/forums/neuro/archive/7830.html

Questions in The Neurology Forum are being answered by doctors from The Cleveland Clinic , consistently ranked one of the best hospitals in America. Subject: Re: myotonic dystrophy and tegretol Forum: The Neurology and Neurosurgery Forum Topic Area: Neurology - General Posted by CCF MD GS on August 29, 1998 at 10:00:37: In Reply to: myotonic dystrophy and tegretol posted by tom on August 27, 1998 at 23:02:23: : I have a pt. c Myotonic Dystrophy. His two sibling daughters live back east and have been started on tegretol for this. I have no information on the use of tegretol for this condition, saw your web site do you know of any studies/ published on the use of tegretol and myotonis dystrophy. a PA in CA Thanks for the question. Wish I had something more to offer you. I did a medline search back 5 years and found no information. The two most effective drugs that have been used to treat myotonia are phenytoin and quinine but their lack of effect in the clinical setting is due mainly to the fact that the myotonia patient is not bothered by the myotonia but by the weakness. If your patient has daughters on this medicine I suggest you contact their doc and ask the purpose of the medication and if they have information regarding its use. Good luck This information is provided for gernal medical education purposes. PLease consult your doctor regarding diagnostic and treatment options.

92. ThatFootSite.com Post New Message. Subject Re myotonic dystrophy. Date/Time Posted on 24 April 2004 at 1253. This fact sheet deals only with myotonic dystrophy. http://www.thatfootsite.com/forum/viewmessage.php?rootid=1907

93. Autosomal Dominant: Myotonic Dystrophy Detailed information on myotonic dystrophy, one types of autosomal dominant condition. Autosomal Dominant myotonic dystrophy. Genes http://www.healthsystem.virginia.edu/uvahealth/peds_genetics/autosom.cfm

@import url(/assets/UVAHealth/ssi/css/greystone_advance.css); Adolescent Medicine Allergy/Asthma/Immunology Blood Disorders Burns Cancer Common Injuries/Poison Tips Craniofacial Anomalies Dermatology Diabetes/Endo/Metabolism Eye Care Genitourinary/Kidney High-Risk Newborn High-Risk Pregnancy Infectious Diseases Medical Genetics Mental Health Nervous System Disorders Normal Newborns Oral Health Orthopaedics Pediatric Surgery Respiratory Disorders Terminal Illness in Children Transplantation FIND A DOCTOR MAKE AN APPOINTMENT CALENDAR OF EVENTS CLINICAL TRIALS Autosomal Dominant: Myotonic Dystrophy Genes are inherited from our biological parents in specific ways. One of the basic patterns of inheritance of our genes is called autosomal dominant inheritance. What is autosomal dominant inheritance? Autosomal dominant inheritance means that the gene is located on one of the autosomes (chromosome pairs 1 through 22). This means that males and females are equally affected, and "dominant" means that only one gene is necessary to have the trait. When a parent has a dominant trait, there is a 50 percent chance that any child they have will also inherit the trait: Click image to enlarge There are four possible combinations in the children. Two of the four, or 50 percent, have inherited the trait. The other 50 percent have not inherited the trait. These four combinations are possible every time a pregnancy occurs between these two individuals. The gender of the children (whether they are sons or daughters) does not matter. The chance is 50/50 for each pregnancy.

94. Smith Michael, Shelia, Whitney and Michael. Contains newsletter, photos and information on myotonic muscular dystrophy. http://myweb.ecomplanet.com/SMIT2157/

95. Facts About Myotonic Muscular Dystrophy | MDA Publications New 10/00. Facts About myotonic Muscular dystrophy. Introduction. Questions and Answers. Does It Run in the Family? MDA's Search for Treatment and Cures. MDA is Here to Help You. INTRODUCTION. Denise http://www.mdausa.org/publications/fa-mmd.html

New 10/00 Facts About Myotonic Muscular Dystrophy Muscular Dystrophy Association Introduction Questions and Answers Does It Run in the Family? MDA's Search for Treatment and Cures ... MDA is Here to Help You INTRODUCTION Denise Balon Dear Friends: Myotonic muscular dystrophy (MMD) has been a part of my family's life for many years. My four siblings and I have symptoms that began in our 30s, and we believe the disease goes back at least two generations before us. Some of my nieces and nephews are also affected. Like many of you, we were surprised to learn that such a wide range of symptoms muscle weakness, involuntary clenching of hands and jaw, swallowing problems, eye problems, heart disorders, extreme fatigue and other difficulties could be caused by a form of muscular dystrophy. With correct information about our disorder, we're able to monitor and protect our health to a great degree. This pamphlet has been prepared to give you the basic knowledge about MMD that you'll need to make your life as enjoyable and productive as possible. With this information, you or your children can be prepared for changes to come and armed to minimize many effects of the disease. By understanding how the disease affects me in different ways, I've been able to continue working as a nurse but in a less physically demanding role. I take pains to keep my stress level to a minimum and make sure I get plenty of sleep, because I've learned that stress and fatigue will exacerbate my symptoms rapidly. A pacemaker corrects the heart problems caused by my MMD.

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