Roche Lexikon Medizin (4. Aufl.) - Hallervorden*-Spatz* Syndrom Translate this page Hallervorden*-Spatz* Syndrom. engl. hallervorden-spatz syndrome Biogr. JULIUS H., 18821965, Neurologe, Gießen HUGO SP. autosomal http://www.gesundheit.de/roche/ro15000/r15041.html
Karger Publishers 2 Sethi KD, Adams RJ, Loring DW, EI Gammal T hallervordenspatz syndrome Clinical and magnetic resonance imaging correlations. Ann Neurol 1988;24692-694. http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowFulltext&ProduktNr=
Membres De La SENP Pediatr Neurol 2001;25(2) Striatal and pontocerebellar hypoperfusion in hallervordenspatz syndrome. Castelnau P, Zilbovicius M, Ribeiro http://www.senp-neuropediatrie.org/Annuaire_des_membres/Liste_des_Membres_de_la_
Extractions: Major akinesia with arthrogryposis and craniosynostosis at birth mimics irreversible disorders of the nervous system of pejorative outcome. In this context, the early detection of anti-acetylcholine fetal receptor antibodies in the mother may allow rapid diagnosis of transient neonatal myasthenia of favorable prognosis.
GREENSEEK hallervordenspatz syndrome Association (HSSA) OMIM National Center for Biotechnology Information. - A clinical synopsis of hallervorden-spatz syndrome. http://www.greenseek.de/internet/index.php/Health/Conditions_and_Diseases/Neurol
Health Library - Founded 1996.Provides emotional support to families affected by hallervordenspatz syndrome, a rare, progressive neurological disorder, resulting in iron http://yalenewhavenhealth.org/Library/HealthGuide/SelfHelp/topic.asp?hwid=shc29h
Extractions: ALS LIKE DISEASES In many countries, ALS is regarded as just one form of several related Motor Neurone Diseases. In these countries the broader (and perhaps more accurate) term "Motor Neurone Disease" is used instead of ALS. There are some symptoms that occur in "textbook" cases of ALS that can differentiate it from other Motor Neurone disorders. The diagnosis of typical or so called "sporadic" ALS requires the presence of upper motor neuron signs (spasticity, rigidity, abnormal reflexes), lower motor neuron signs (weakness, atrophy) and progression. The pattern of upper and lower motor neuron signs that a neurologist detects are usually found in certain patterns commonly spread throughout several regions of the body. EMG and nerve conduction studies are helpful in identifying lower motor neuron problems in areas where there may not be much weakness. There are a large number of other illnesses that share some or many features of ALS and they must be evaluated or ruled out before a definite diagnosis can be made. An experienced practitioner who is familiar with the many presentations of ALS can make an accurate diagnosis with appropriate diagnostic testing and time to ensure that "look-alike" diseases have been excluded. OTHER MOTOR NEURON DISEASES Primary Lateral Sclerosis This motor neuron disease is similar to ALS but only the upper motor neurons are degenerating. Although rare, some lower motor neurons may appear to be involved with mild atrophy. PLS patients have most problems with spasticity and stiffness. The disease can progress slowly over many years. Patients often respond well to medical therapy to reduce their spasticity and stiffness.
BBC NEWS | Health | Gene Test For Rare Brain Disease area of the brain. Prof Jane Gitschier. The genetic disease, known as hallervordenspatz syndrome (HSS), affects the basal ganglia. http://news.bbc.co.uk/2/hi/health/2617337.stm
Extractions: Scientists have developed a new test for a rare brain disorder similar to Parkinson's Disease. They have found that all patients have a distinctive pattern of brain changes which can be detected by scanning. We are now working to figure out why these defects lead to cell death and iron accumulation in this very specific area of the brain The genetic disease, known as Hallervorden-Spatz Syndrome (HSS), affects the basal ganglia. A number of neurological disorders, including Parkinson's, Huntingdon's disease and Tourette's syndrome, are also believed to arise from problems in this part of the brain. Researchers hope the test could lead to a better understanding of what goes wrong as well as improved diagnosis of the rare condition. Slow progression HSS is an inherited, neurological movement disorder marked by a progressive decline of the nervous system.
Extractions: Hallervorden-Spatz (syndrome d) Voir également hypertonie, globus pallidus, locus niger, pigment. En anglais : Hallervorden-Spatz's syndrome. Affection familiale rare, débutant dans l'enfance par des troubles de la marche qui sont secondaires à un excès de tonicité musculaire (hypertonie) des membres inférieurs et de tout le corps. Au cours de ce syndrome, en rapport avec la dégénérescence d'une zone du cerveau (le globus pallidus et le locus niger) qui est envahie par des pigments contenant du fer, la parole et la déglutition (avaler quelque chose) sont très difficiles. Il s'y ajoute d'autre part une agitation psychique et des mouvements involontaires. Cause
Extractions: (Hallervorden-Spatz Syndrome; late infantile neuroaxonal dystrophy; Neuroaxonal Dystrophy, Late Infantile; Pigmentary Degeneration of Globus Pallidus, Substantia Nigra, Red Nucleus; pigmentary pallidal degeneration syndrome; Progressive Pallid Degeneration Syndrome; progressive pallidal degeneration syndrome) Revised and Updated for the Internet Age P A P E R B A C K Paperback Book Paperback Book Order by phone: 800-843-2665 (within USA) 1-201-272-3651 (from outside USA) Paperback Book Shipped in 3 to 5 business days E B O O K Electronic File * E-Book version sent via e-mail in 2 business days Electronic File *E-Book version sent via e-mail in 2 business days Pages Price $28.95(USD) ISBN Published Synopsis A comprehensive manual for anyone interested in self-directed research on Hallervorden-Spatz Disease. Fully referenced with ample Internet listings and glossary. Related Conditions/Synonyms Hallervorden-Spatz Syndrome; late infantile neuroaxonal dystrophy; Neuroaxonal Dystrophy, Late Infantile; Pigmentary Degeneration of Globus Pallidus, Substantia Nigra, Red Nucleus; pigmentary pallidal degeneration syndrome; Progressive Pallid Degeneration Syndrome; progressive pallidal degeneration syndrome Description Table of Contents Introduction Overview Organization Scope Moving Forward PART I: THE ESSENTIALS Chapter 1. The Essentials on Hallervorden-Spatz Disease: Guidelines
Ha : On Medical Dictionary Online syndrome Hallermann s syndrome HallermannStreiff syndrome Hallermanns syndrome Hallervorden Spatz Disease Hallervorden Spatz syndrome hallervorden-spatz http://www.online-medical-dictionary.org/?q=~Ha
Hallervorden-spatz, Maladie : Arborescences MeSH Translate this page du motclef page CISMeF du motclef hallervorden-spatz, maladie C10.228.140.079.493 page PubMed du motclef page CISMeF du motclef meige, syndrome C10.228.140 http://www.chu-rouen.fr/navimesh/H/navihallervordenspatzmaladie.html
Neurology -- Abstracts: Ching Et Al. 58 (11): 1673 is a rare syndrome with many clinical similarities to pantothenate kinaseassociated neurodegeneration (PKAN, formerly HallervordenSpatz syndrome). http://www.neurology.org/cgi/content/abstract/58/11/1673
Extractions: Brief Communications K. H.L. Ching, BS S. K. Westaway, PhD J. Gitschier, PhD J. J. Higgins, MD and S. J. Hayflick, MD From the Departments of Molecular and Medical Genetics (Drs. Hayflick and Westaway, and K. Ching), Pediatrics and Neurology (Dr. Hayflick), School of Medicine, Oregon Health and Science University, Portland; Howard Hughes Medical Institute and Departments of Medicine and Pediatrics (Dr. Gitschier), University of California, San Francisco; and Center for Human Genetics and Child Neurology (Dr. Higgins), Mid Hudson Family Health Institute, New Paltz, NY. Address correspondence and reprint requests to Dr. S. Hayflick, Department of Molecular and Medical Genetics, OHSU, L-103a, Portland, OR 97201-3098; e-mail:
