1. Hallervorden-Spatz Syndrome (www.whonamedit.com) hallervordenspatz syndrome A very rare disease with degeneration of the globuspallidus, red nucleus, and substantia nigra of the brain. http://www.whonamedit.com/synd.cfm/1082.html

Home List categories Eponyms A-Z Biographies by country ... Contact Whonamedit.com does not give medical advice. This survey of medical eponyms and the persons behind them is meant as a general interest site only. No information found here must under any circumstances be used for medical purposes, diagnostically, therapeutically or otherwise. If you, or anybody close to you, is affected, or believe to be affected, by any condition mentioned here: see a doctor. A recommendation: Hypography is an open community about science and all things related Hallervorden-Spatz syndrome Also known as: Hallervorden-Spatz disease Gilman and Barrett neuroaxonal dystrophy type I Synonyms: Localized neuroaxonal dystrophy, late infantile neuroaxonal dystrophy, progressive pallidal degeneration syndrome, progressive pallidal degeneration or adult amaurotic idiocy, pigmentary degeneration syndrome of globus pallidus, substantia nigra and red nucleus, pallidoreticular pigment degeneration, progressive pallidal degeneration syndrome. Associated persons: Robert E. Barrett

2. Redirect A clinical synopsis of hallervordenspatz syndrome. http://www3.ncbi.nlm.nih.gov/htbin-post/Omim/dispmim?234200

3. Hallervorden-Spatz Disease An article about HallervordenSpatz disease, with an explanation, the symptoms and prognosis. http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

4. Hallervorden-Spatz Syndrome - Pigmentary Pallidal Degeneration - Information Pag A rare autosomal recessive degenerative disorder which usually presents in late http://www.hon.ch/HONselect/RareDiseases/EN/C10.228.140.079.493.html

InitBulle("navy","#F8F8F8","#000066",1); HONcode sites All Web sites HONselect News ... Images HONselect Search English French German Spanish Portuguese the word the part of word in MeSH term in MeSH term and description Information on "Hallervorden-Spatz Syndrome": Medical hierarchy and definition Research Articles Web resources Medical Images Medical News Medical Conferences Clinical Trials Hierarchy English French German Spanish Portuguese Hallervorden-Spatz Syndrome Definition: A rare autosomal recessive degenerative disorder which usually presents in late childhood or adolescence. Clinical manifestations include progressive MUSCLE SPASTICITY ; hyperreflexia; MUSCLE RIGIDITY DYSTONIA DYSARTHRIA Synonym(s): Pigmentary Pallidal Degeneration / Hallervorden-Spatz Disease / Pigmentary Pallidal Atrophy / Atrophies, Pigmentary Pallidal / See Related: Muscle Rigidity Dystonia Dysarthria Muscle Spasticity ... New search Web resources for "Hallervorden-Spatz Syndrome" English French = Site with HON description - = Site with a robot description info: enter the site: (click below) domain of the site: HONcode - eMedicine - Hallervorden-Spatz Disease : Article by Neeta Garg, MD

5. NORD - National Organization For Rare Disorders, Inc. Offers synonyms, a general discussion and further resources for the disorder formerly known as hallervordenspatz syndrome. http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Neurodegenera

6. Hallervorden-Spatz Syndrome (www.whonamedit.com) hallervordenspatz syndrome A very rare disease with degeneration of the globus pallidus, red nucleus, and substantia nigra of the brain. It is http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

7. HONselect - Hallervorden-Spatz Syndrome Translate this page English, hallervorden-spatz syndrome, - Pigmentary Pallidal Degeneration -Hallervorden-Spatz Disease - Pigmentary Pallidal Atrophy http://www.hon.ch/HONselect/RareDiseases/C10.228.140.079.493.html

List of rare diseases: English Deutsch Language: MeSH term: Accepted terms: English: Hallervorden-Spatz Syndrome - Pigmentary Pallidal Degeneration - Hallervorden-Spatz Disease - Pigmentary Pallidal Atrophy - Atrophies, Pigmentary Pallidal - Atrophy, Pigmentary Pallidal - Degeneration, Pigmentary Pallidal Français: Maladie de Hallervorden-Spatz - Dégénérescence du globus pallidus de Hallervorden Spatz Deutsch: Hallervorden-Spatz-Syndrom - Globus-pallidus-Pigmentdegeneration - Pallidoretikuläre Pigmentdegeneration Español: Degeneración Palidal Pigmentaria Português: Síndrome de Hallervorden-Spatz - Degeneração Palidal Pigmentar HONselect ressources Definition: Yes Articles: Yes Images: No News: No Conferences: No Clinical trials: No Web sites: English Yes Français Yes Deutsch No Español No Português No Home About us Site map Search ... Contact http://www.hon.ch/HONselect/RareDiseases/C10.228.140.079.493.html Last modified: Wed May 18 2005

8. NORD - National Organization For Rare Disorders, Inc. Neurodegeneration with Brain Iron Accumulation, formerly hallervordenspatz syndrome (Letter of intent and abstract due April 13, 2005) http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

9. Hallervorden-Spatz Syndrome Links to information and resources for hallervordenspatz syndrome, an inheritedneurological movement disorder. http://rarediseases.about.com/cs/hallervordenspatz/

zJs=10 zJs=11 zJs=12 zJs=13 zc(5,'jsc',zJs,9999999,'') zfs=0;zCMt='a70' About Rare / Orphan Diseases Rare Diseases Essentials ... Help zau(256,140,140,'el','http://z.about.com/0/ip/417/C.htm','');w(xb+xb+' ');zau(256,140,140,'von','http://z.about.com/0/ip/496/6.htm','');w(xb+xb); FREE Newsletter Sign Up Now for the Rare / Orphan Diseases newsletter! See Online Courses Search Rare / Orphan Diseases Hallervorden-Spatz Syndrome Guide picks An inherited neurological movement disorder characterized by iron deposits in the brain, leading to progressive degeneration of the nervous system. MCW Health Link Brief information on the disorder from the Medical College of Wisconsin. NINDS: Hallervorden-Spatz Disease Information on the syndrome from the National Institute for Neurological Disorders and Stroke. NORD: Hallervorden-Spatz Disease Brief definition of the disorder from the National Organization for Rare Disorders (NORD). OHSU: Hallervorden-Spatz Syndrome Good overview of the Hallervorden-Spatz disorders and Oregon Health Science University research, by Susan J. Hayflick, MD. Topic Index Email to a Friend Our Story Be a Guide ... Patent Info.

10. Hallervorden-Spatz Disease HALLERVORDENSPATZ DISEASE http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

11. Hallervorden-Spatz Syndrome Gene Discovery [NEI News And Events] National Eye Institute s NEI News and Events Web site covers all the news NEIpress releases, upcoming events, conferences and meetings, http://www.nei.nih.gov/news/statements/hallervorden-spatz.asp

Text size: S M L Health Funding News Laboratories ... Statements and Reports on Vision News and Events NEI Statement Hallervorden-Spatz Syndrome Gene Discovery National Eye Institute National Institutes of Health The gene that causes Hallervorden-Spatz syndrome has been identified by National Eye Institute (NEI) grantees. Hallervorden-Spatz syndrome is a rare, inherited, neurological disorder associated with high accumulations of iron in the brain, and causes progressive degeneration of the retina and nervous system. The new findings appear in the August 2001 issue of Nature Genetics. Susan J. Hayflick, MD, associate professor of Molecular and Medical Genetics at Oregon Health Sciences University in Portland, and colleagues discovered that the defective gene produces an ineffective enzyme. The body needs the normal enzyme to utilize vitamin B5; without it, vitamin B5 cannot produce some of the body's essential compounds. The ineffective enzyme results in Hallervorden-Spatz syndrome. Because of this research, scientists can now focus their efforts on developing treatment strategies that bypass this defective enzyme, allowing the body to utilize vitamin B5 to help make the essential body compounds. Researchers can also look toward developing a genetic diagnostic test for the syndrome. Understanding the biochemical defects in Hallervorden-Spatz syndrome may also provide insights into the effect iron has on other neurodegenerative diseases associated with high iron accumulations, such as Parkinson's disease.

12. Hallervorden-Spatz Disease Neurodegeneration with Brain Iron Accumulation(HallervordenSpatz disease) information sheet compiled by the National Institute of Neurological http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

13. Congressional Justifications FY2003 [NEI News And Events] Discovery of Gene for hallervordenspatz syndrome. hallervorden-spatz syndrome (HSS)is a rare, inherited, neurological disorder associated with high http://www.nei.nih.gov/news/congressjust/cj2003.asp

Text size: S M L Health Funding News Laboratories ... Congressional Justifications News and Events Congressional Justification for FY 2003 National Eye Institute Introduction Science Advances and Future Research Directions Health Disparities Healthy People 2010 ... NEI Budget Policy Authorizing Legislation: Section 301 of the Public Health Service Act, as amended. Reauthorizing legislation will be submitted. Budget Authority: 2001 Actual 2002 Appropriation 2002 Current Estimate 2003 Estimate Increase or Decrease Current Law BA Accured Costs Proposed Law BA FTE This document provides justification for the Fiscal Year 2003 activities of the National Eye Institute (NEI), including HIV/AIDS activities. A more detailed description of NIH-wide Fiscal Year 2003 HIV/AIDS activities can be found in the NIH section entitled "Office of AIDS Research (OAR). The President's appropriations request of $631,818,000 for this account includes current law adjusted by assuming Congressional action on the proposed Managerial Flexibility Act of 2001. Introduction TOP Story of Discovery Providing Sight to Dogs Born Blind.

14. OMIM National Center For Biotechnology Information. A clinical synopsis of hallervordenspatz syndrome. http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

15. Adenoid Cystic Carcinoma, Mastocytosis, Hallervorden-Spatz Syndrome ADENOID CYSTIC CARCINOMA, MASTOCYTOSIS, hallervordenspatz syndrome - NORD.The National Organization for Rare Disorders is seeking applications for 1-year http://vpr2.admin.arizona.edu/rso/02041210.htm

ADENOID CYSTIC CARCINOMA, MASTOCYTOSIS, HALLERVORDEN-SPATZ SYNDROME - NORD The National Organization for Rare Disorders is seeking applications for 1-year grants for clinical studies related to the early detection, diagnosis, or treatment of patients with 1) adenoid cystic carcinoma; 2) Hallervorden-Spatz syndrome; and 3) mastocytosis. Grants provide up to $30,000 for 1 year. Contact: NORD, Research Grant Program, 100 Rt. 37, P.O. Box 8923, New Fairfield, CT 06812-8923. Web: http://www.rarediseases.org/ E-mail: lcataldo@rarediseases.org Telephone: (800) 999-6673. Fax: (203) 746-6481. Deadline: 15 May 2002 for letters of intent; 1 August 2002 for invited full proposals. RSO Reference No.:

16. NEJM Genetic, Clinical, And Radiographic Delineation Of Original Article from The New England Journal of Medicine Genetic, Clinical, and Radiographic Delineation of hallervordenspatz syndrome http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

17. Pantothenate Kinase Associated Neurodegeneration (Hallervorden - Spatz Syndrome) hallervordenspatz syndrome is a rare autosomal recessive hereditary condition Hallervorden - Spatz syndrome (HSS) OMIM 234200 is an autosomal http://www.ijppediatricsindia.org/article.asp?issn=0019-5456;year=2005;volume=72

18. Late Adult Onset Chorea With Typical Pathology Of Late adult onset chorea with typical pathology of hallervordenspatz syndrome D A Grimesa, A E Langb, C Bergeronc http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

19. Pantothenate Kinase Associated Neurodegeneration (Hallervorden - Spatz Syndrome) hallervordenspatz syndrome is a rare autosomal recessive hereditary conditioncharacterized by early onset of progressive movement alteration that include http://www.ijppediatricsindia.org/article.asp?issn=0019-5456;year=2005;volume=72

20. Late Adult Onset Chorea With Typical Pathology Of Short report. Late adult onset chorea with typical pathology of hallervordenspatz syndrome D A Grimesa, A E Langb, C Bergeronc http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

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