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         Torsion Dystonia:     more detail
  1. Blepharospasm-oromandibular dystonia syndrome (Brueghel's syndrome). A variant of adult-onset torsion dystonia? by C. D Marsden, 1976

81. Wuup.de - /Health/Conditions_and_Diseases/Neurological_Disorders
Translate this page torsion dystonia. Siehe auch Links. » Medicine Net torsion dystonia - A brief description of this disorder, its onset and symptoms.
http://wuup.de/index.php/Health/Conditions_and_Diseases/Neurological_Disorders/M

82. Dystonia
Some patterns of dystonia are defined as specific syndromes torsion dystonia, previously called dystonia musculorum deformans or DMD, is a rare, generalized
http://www.herbs4st.com/dystonia.htm
This site is my personal experience with the dystonia, spasmodic torticollis, ST. Read my spasmodic torticollis success story using alternative health methods of herbs, herbal remedies, essential oils, enzymes, homeopathic, aromatherapy, nutrition, diet, vitamins, minerals, and massage. Learn about dystonia, herbs, essential oils, enzymes, general health, spasmodic torticollis, ST, alternative health program for torticollis, supplements for ST, and nutritional surveys.
DYSTONIA
What are the dystonias?
The dystonias are movement disorders in which sustained muscle contractions cause twisting and repetitive movements or abnormal postures. The movements, which are involuntary and sometimes painful, may affect a single muscle; a group of muscles such as those in the arms, legs, or neck; or the entire body. Diminished intelligence and emotional imbalance are not usually features of the dystonias.
What are the symptoms?
Early symptoms may include a deterioration in handwriting after writing several lines, foot cramps, and a tendency of one foot to pull up or drag after running or walking some distance. The neck may turn or pull involuntarily, especially when tired. Other possible symptoms are tremor and voice or speech difficulties. The initial symptoms can be very mild and may be noticeable only after prolonged exertion, stress, or fatigue. Over a period of time, the symptoms may become more noticeable and widespread and be unrelenting; sometimes, however, there is little or no progression.

83. LCD For
333.6, IDIOPATHIC torsion dystonia. 333.7, SYMPTOMATIC torsion dystonia. 333.81, BLEPHAROSPASM. 333.89, OTHER FRAGMENTS OF torsion dystonia.
http://www.ahsmedicare.com/medical_review_appeals/provider/lmrp/active/BOTULINUM
Associated Hospital Service
To Active Policies
LCD for BOTULINUM TOXIN TYPE A
Contractor Information Contractor Name Associated Hospital Service Contractor Number Contractor Type FI
LCD Information LCD Database ID Number LCD Title BOTULINUM TOXIN TYPE A Contractor's Determination Number FI-R-0304-09AC CMS National Coverage Policy 1) Title XVIII of the Social Security Act, Section Coverage Policy 1862(a)(1)(A) allows coverage and payment for only those services that are considered to be medically reasonable and necessary.
2) Title XVIII of the Social Security Act, section 1862 (a) (7) and 42 Code of Federal Regulations, section 411.15 et.seq. This section excludes routine physical examinations.
3) Title XVIII of the Social Security Act, section 1833 (e). This section prohibits Medicare payment for any claim which lacks the necessary documentation to process the claim.
Primary Geographic Jurisdiction Massachusetts
Maine
Secondary Geographic Jurisdiction
Massachusetts
Maine
Oversight Region Region I CMS Consortium Northeast Original Determination Effective Date Original Determination Ending Date Revision Effective Date Revision Ending Date Indications and Limitations of Coverage and/or Medical Necessity Botulinum toxin type A is indicated for spastic
conditions that have been unresponsive to conventional treatment, including medication and physical therapy.

84. GeneCard For DYT1
years. Genatlas disease DYT1 idiopathic torsion dystonia,with childhood limbonset,progressive,frequent in Jewish patients. GeneTests
http://genecards.bcgsc.ca/cgi-bin/carddisp?DYT1

85. Gary Heiman, Ph.D., Bibolography
D, Burke R, Fahn S, Risch N, Breakefield XO, Kramer P. A study of idiopathic torsion dystonia in a nonJewish family Evidence for genetic heterogeneity.
http://cpmcnet.columbia.edu/dept/sph/epi/gcd/heiman-refs.html
TRAINING PROGRAM Description People Application Stipend Selected publications for Gary A. Heiman , Ph.D.
Knowles JA, Fyer AJ, Vieland VJ, Weissman MM, Hodge SE, Heiman GA, Haghighi F, de Jesus GM, Rassnick H, Preud'homme-Rivelli X, Austin T, Cunjak J, Mick S, Fine LD, Woodley KA, Das K, Maier W, Adams PB, Freimer NB, Klein DF, and Gilliam TC. Results of a genome-wide genetic screen for panic disorder. Am J Med Genet (Neuropsychiat Genet) 81: 139-147, 1998.
Saunders-Pullman R, Shriberg J, Heiman GA, Raymond R, Wendt K, Kramer P, Schilling K, Kurlan R, Klein C, Ozelius LJ, Risch NJ, PhD and Bressman SB. The spectrum of myoclonus dystonia: Possible association with OCD and alcohol dependence. Neurology 58: 242-245, 2002.
Ahsan H, Hodge SE, Heiman GA, Begg MD and Susser ES. Relative risk for genetic associations: the case-parent triad as a variant of case-cohort design. Int. J. Epidemiol. 31(3): 669-678, 2002.

86. Torsion Dystonia Health Information Beverly Farms Oxaluria See Hyperoxaluria Med
health care provider carls fact jr parkinsons progression conditions. bueno information taco public health condition eyebrow piercing
http://www.health-condition.us/beldenville_840993.html
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87. Wauu.DE: Health: Conditions And Diseases: Neurological Disorders: Movement Disor
Wauu.DE Health Conditions and Diseases Neurological Disorders Movement Disorders torsion dystonia.
http://www.wauu.de/Health/Conditions_and_Diseases/Neurological_Disorders/Movemen
Home Health Conditions and Diseases Neurological Disorders ... Movement Disorders : Torsion Dystonia Search DMOZ-Verzeichnis:
All Categories Categories Onlye
Links:
  • Medicine Net: Torsion Dystonia
    A brief description of this disorder, its onset and symptoms.
    http://www.medterms.com/script/main/art.asp?articlekey=5822
  • Pediatric Database
    A definition of torsion dystonia, the epidemiology, pathogenesis, clinical features, investigations and management.
    http://www.icondata.com/health/pedbase/files/IDIOPAT2.HTM
  • University of Pittsburgh
    From the Genetics Education and Counseling Program a brochure about Torsion Dystonia.
    http://www.pitt.edu/~edugene/Torsion.pdf
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88. Health Care Thoracic Medicine Torsion Dystonia First Aid First Aid Temporomandib
health mental oakland wellness prevention tanning. state resources medical resource healthy choking diseases huntington s foot hand
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89. Blackwell Synergy - Cookie Absent
Mutations in torsinA underlie early onset torsion dystonia, an autosomal dominant, neurologically based movement disorder. TorsinB
http://www.blackwell-synergy.com/links/doi/10.1111/j.1471-4159.2004.02404.x/enha
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90. Hum. Mol. Genet. -- Abstracts: Klein Et Al. 7 (7): 1133
recently has been cloned and shown to contain a three nucleotide (GAG) deletion responsible for most cases of autosomal dominant earlyonset torsion dystonia.
http://hmg.oupjournals.org/cgi/content/abstract/7/7/1133
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ARTICLES
De novo mutations (GAG deletion) in the DYT1 gene in two non-Jewish patients with early-onset dystonia
C Klein, MF Brin, D de Leon, SA Limborska, IA Ivanova-Smolenskaya, SB Bressman, A Friedman, ED Markova, NJ Risch, XO Breakefield and LJ Ozelius
Molecular Neurogenetics Unit, Neurology Service, Massachusetts General Hospital and Department of Neurology and Genetics, Harvard Medical School, Boston, MA, USA. The DYT1 gene recently has been cloned and shown to contain a three nucleotide (GAG) deletion responsible for most cases of autosomal dominant early-onset torsion dystonia. This deletion results in the loss of one of a

91. Hum. Mol. Genet. -- Abstracts: Leube Et Al. 5 (10): 1673
Idiopathic torsion dystonia assignment of a gene to chromosome 18p in a German family with adult onset, autosomal dominant inheritance and purely focal
http://hmg.oupjournals.org/cgi/content/abstract/5/10/1673
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ARTICLES
Idiopathic torsion dystonia: assignment of a gene to chromosome 18p in a German family with adult onset, autosomal dominant inheritance and purely focal distribution
B Leube, D Rudnicki, T Ratzlaff, KR Kessler, R Benecke and G Auburger
Department of Neurology, University Hospital, Dusseldorf, Germany. Idiopathic torsion dystonia (ITD) is a group of movement disorders which is usually inherited in an autosomal dominant manner with reduced penetrance. Most patients with ITD present with focal dystonia at adult age. However, thus far, this common subform remained unmapped chromosomally. In contrast, a rare early onset, more generalized form of ITD has been mapped to

92. Baillement-van.sweden
torsion dystonia ? CD Marsden
http://webperso.easyconnect.fr/baillement/dystonia.html

93. Evaluation And Treatment Of Dystonia
Bressman et al 9 studied 174 Ashkenazi Jewish patients with idiopathic torsion dystonia and identified genetic linkage to chromosome 9q34, the DYT1 gene.
http://www.medscape.com/viewarticle/410595_4

94. Re: Another Question Regarding Anesthesia & Dystonia
. You may be aware of cases of oculogyric crises precipitated by anesthesia in people who have idiopathic torsion dystonia. The
http://www.medhelp.org/forums/neuro/archive/13878.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:
Forum: The Neurology and Neurosurgery Forum
Topic Area: Dystonia
Posted by CCF MD mdf on December 18, 1998 at 10:08:58:
In Reply to: posted by Erin on December 17, 1998 at 15:05:19:
: I have a more complicated question regarding this. Can general anesthesia
: cause dystonia (not temporary) which cannot be corrected with benedryl but
: responds to Sinemet? Or is generalized dystonia, which is dopa-responsive,
: definitely a hereditary form of dystonia? I am asking these questions to
: help us decide whether to pursue genetic testing for dystonia. Our daughter's : severe onset of Dystonia began shortly after a tonsilectomy and this same : surgery may need to be done for another daughter. Needless to say, we are hesitant about : considering surgery for her. I understand how difficult dystonia is to : diagnose and treat, let alone find the cause, but any input would be : appreciated. There is a strong history of spinocerebellar degeneration

95. HEADLINE Scientists Find Gene Defect At Heart Of Crippling
NEWSPAPER ARTICLE SYNOPSIS Scientists identified the defective gene DYT1 as the cause of early onset torsion dystonia, a disabling disorder with extreme
http://library.uchc.edu/bhn/bhn95-97/cite95-97/nyt95-97/33dys.txt
HEADLINE: Scientists find gene defect at heart of crippling ailment. NEWSPAPER ARTICLE SYNOPSIS: Scientists identified the defective gene DYT1 as the cause of early onset torsion dystonia, a disabling disorder with extreme muscle contractions that often begins in childhood. NEWSPAPER ARTICLE SOURCE: Associated Press. Scientists find gene defect at heart of crippling ailment. New York Times 1997 September 9 : C6 (col. 5). JOURNAL ARTICLE CITATION: Ozelius LJ, et. al. Early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein. Nature Genetics 1997 September;17(1):40-48. jsk 9/9/97

96. Dystonia Medical Research Foundation: Home Page
Home page of the dystonia Medical Research Foundation. Links to pages on all aspects of the movement disorder dystonia (blepharospasm, spasmodic torticollis, spasmodic dysphonia, writer's cramp).
http://www.dystonia-foundation.org/
May, 2004
Dear Foundation Friends-
Dystonia Awareness Week is fast approaching - June 5-12, 2004 - and I hope you are making plans to celebrate with us. Working together, we can accomplish so much.
more

Fleisher Receives Leadership Award from AAN

Bachmann-Strauss Receives Proceeds from Jenny Craig Book

Musicians With Dystonia Program
... Contact
The design and implementation of the Dystonia Foundation's website was made possible by a generous educational grant from the Allergan Foundation.

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