21. SPECS Condition Specific Organisations We are pleased to be associated with the following organisations Albinism Fellowship.alstrom syndrome UK. Aniridia Network. British Retinitas Pigmentosa Society. http://www.eyeconditions.org.uk/ORGSpecific.htm

SP ecific E ye C ondition S Registered charity number 1095813. www.eyeconditions.org.uk Condition Specific Support Groups: Although the charities, support groups and organisations listed in this directory are UK based they will all extend a warm welcome to visitors from overseas. They will be glad to help you themselves or may have information about similar organisations in your home country. If you do not know the exact nature of your condition you may wish to search the site or contact some of the groups offering generic support to people and families with eye conditions. We are pleased to be associated with the following organisations: Albinism Fellowship Alstrom Syndrome UK Aniridia Network British Retinitas Pigmentosa Society ... CHARGE Family Support Group (external link) Charles Bonnett Syndrome CLIMB (Children Living with Metabolic Disorders) Cohen Syndrome Support Group National Diabetic Retinopathy Network Diabetes UK The Dystonia Society ... Osteopetrosis Support Trust Pete's Anomaly PLAN (People with Lebers Amaurosis Network) PiXiE - The Pseudoxanthorna Elasticum (PXE) Support Group Retinoblastoma Society Stargardt Support Group Stickler Syndrome Support Group Sturge Weber Foundation (UK) SWAN (Syndromes Without A Name) Tadpole ... Thyroid Eye Disease Usher Syndrome Uveitis Information Group Wolfram Syndrome If you represent an organisation working with eye conditions and would like to be listed in the directory, please

22. Entrez-PubMed Click here to read alstrom syndrome further evidence for linkage tohuman chromosome 2p13. Collin GB, Marshall JD, Boerkoel CF, Levin http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=1

23. Entrez-PubMed alstrom syndrome. Report OBJECTIVE The authors report 22 cases of Alstromsyndrome (AS), which is the largest series to date. Only http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=9

24. NORD - National Organization For Rare Disorders, Inc. alstrom syndrome. To purchase fulltext report ($7.50) View Cart/Checkout.Copyright 1994, 1996, 2002 Synonyms of alstrom syndrome ALMS. http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Alstrom Syndr

25. NORD - National Organization For Rare Disorders, Inc. Alkaptonuria Allan Herndon Syndrome Alopecia Areata Alpers Disease Alpha1-AntitrypsinDeficiency Alport Syndrome alstrom syndrome Alternating Hemiplegia of http://www.rarediseases.org/search/rdblist.html

Search NORD's Databases NORD maintains three searchable databases and an alphabetical index of disease names. Index of Rare Diseases The A-to-Z of Rare Diseases Rare Disease Database Read about more than 1,100 rare diseases. View sample report Organizational Database Find a support group or other source of help. Orphan Drug Designation Database Find out about new and experimental orphan products. Database Subscriptions Subscriptions provide complete access to NORD's databases at libraries, schools, universities, and hospitals. NORD's Washington Office Read about events on Capitol Hill, funding for rare-disease research, and other topics of interest from NORD's office in Washington, DC. 5 Oxoprolinuria ACTH Deficiency AIDS (Acquired Immune Deficiency Syndrome) AIDS Dysmorphic Syndrome ... HOME Last modified Sunday, February 02, 2003

26. Alstrom Syndrome : Meddie Health Search alstrom syndrome Contains information about this syndrome, medical references, InternationalSociety for alstrom syndrome Families (SASF), and other resources. http://www.meddie.com/search/Health/Conditions_and_Diseases/Rare_Disorders/Alstr

HOME ADD A LINK MODIFY A LINK NEW LINKS ... TOP RATED Search Meddie: the entire directory only this category More search options Home Health Conditions and Diseases ... Rare Disorders : Alstrom Syndrome ITEMS: LINKS: Alstrom Syndrome Contains information about this syndrome, medical references, International Society for Alstrom Syndrome Families (SASF), and other resources. (Rating: 0.00 Votes: 0) Rate It Alstrom Syndrome UK Support Group Information centre and discussion forum for anyone with an interest in this disorder. (Rating: 0.00 Votes: 0) Rate It HOME ADD A LINK MODIFY A LINK ... Design © ISC Enterprises Inc.

27. Rare Disorders : Meddie Health Search CATEGORIES Agnosia (5). Aicardi Syndrome (8). alstrom syndrome (4). Barth Syndrome(3). Cerebrocostomandibular Syndrome (5). Cleidocranial Dysplasia (5). http://www.meddie.com/search/Health/Conditions_and_Diseases/Rare_Disorders/

HOME ADD A LINK MODIFY A LINK NEW LINKS ... TOP RATED Search Meddie: the entire directory only this category More search options Home Health Conditions and Diseases : Rare Disorders CATEGORIES: Agnosia Aicardi Syndrome Alstrom Syndrome Barth Syndrome ... Wegener's Granulomatosis ITEMS: LINKS: Contact a Family Information about this organization as well as the CaF directory of specific conditions and rare disorders. Also details about the Rare Disorders Alliance - UK. (Rating: 0.00 Votes: 0) Rate It Human Growth Foundation Information about growth-related disorders through education, research, and advocacy. Member driven organization. (Rating: 0.00 Votes: 0) Rate It International Rare Disease Support Network A community providing more than a 1000 different links to support groups for the people of all nations. (Rating: 0.00 Votes: 0) Rate It National Organization for Rare Disorders, Inc. Information about NORD, its programs, special events and the variety of services offered. Includes a rare disease, organization and orphan drug database. Diseases are listed alphabetically for easy searching. (Rating: 0.00 Votes: 0)

28. Health Ency.: Disease: Alstrom Syndrome alstrom syndrome. Alternative names AlstromHallgren syndrome; Alstroem'sretino-otodiabetic syndrome. Definition an inherited disease http://www.accessatlanta.com/shared/health/adam/ency/article/001665.html

SEARCH: The Web Yellow Pages HOME AJC.COM Illustrated Health Encyclopedia Important notice Ency. home Disease A Alstrom syndrome Overview Symptoms Treatment Alternative names: Alstrom-Hallgren syndrome; Alstroem's retino-otodiabetic syndrome Definition: an inherited disease characterized by progressive blindness juvenile onset diabetes mellitus, obesity deafness , and normal mental capacity. Causes and Risks This is an autosomal recessive , inherited disorder. It is extremely rare. The syndrome has a higher incidence in Holland and Sweden. Ency. home Disease A Please read this Important notice Also Check Out Subscribe to The Atlanta Journal-Constitution Home Autos Classifieds ... Our Sponsors By using AccessAtlanta.com you accept the terms of our Visitor Agreement . Please read it. Privacy statement Registered site users: edit your profile

29. Health Ency.: Disease: Alstrom Syndrome alstrom syndrome. Alternative names AlstromHallgren syndrome; Alstroem's retino-otodiabeticsyndrome. Treatment. There is no treatment for this syndrome. http://www.accessatlanta.com/shared/health/adam/ency/article/001665trt.html

SEARCH: The Web Yellow Pages HOME AJC.COM Illustrated Health Encyclopedia Important notice Ency. home Disease A Alstrom syndrome Overview Symptoms Treatment Alternative names: Alstrom-Hallgren syndrome; Alstroem's retino-otodiabetic syndrome Treatment There is no treatment for this syndrome. Prognosis Permanent blindness is likely to develop. Complications Complications related to diabetes mellitus can occur. Call Your Health Care Provider If: Call your health care provider if you suspect symptoms of diabetes mellitus such as increased thirst and urination.Call as soon as you suspect that your infant or child cannot see or hear normally. Ency. home Disease A Please read this Important notice Also Check Out Subscribe to The Atlanta Journal-Constitution Home Autos Classifieds ... Our Sponsors By using AccessAtlanta.com you accept the terms of our Visitor Agreement . Please read it. Privacy statement Registered site users: edit your profile

30. Homozygosity Mapping At Alstrom Syndrome To Chromosome 2p. Homozygosity mapping at alstrom syndrome to chromosome 2p. CollinGB, Marshall JD, Cardon LR and Nishina PM Hum Mol Genet (1997) 6 http://bioinformatics.well.ox.ac.uk/~lon/Pubs/0009063741.html

Homozygosity mapping at Alstrom syndrome to chromosome 2p. Collin GB, Marshall JD, Cardon LR and Nishina PM Hum Mol Genet Alstrom syndrome is a rare autosomal recessive disorder characterized by pigmentary retinal degeneration, sensorineural hearing loss, childhood obesity, non-insulin-dependent diabetes mellitus, hyperlipidemia and chronic nephropathy. Features occasionally observed include acanthosis nigricans, hypogonadism, hypothyroidism, alopecia, short stature and cardiomyopathy. We report here the results of a linkage study in a large French Acadian kindred, as a first step in identifying the molecular basis of Alstrom syndrome. Evidence of a founder effect made if feasible to use a homozygosity mapping strategy to identify the chromosomal location of the Alstrom gene. In a genome-wide screen, haplotype sharing for a region on chromosome 2 was observed in all affected individuals. Two point linkage analysis resulted in a maximum lod score of 3.84 (theta = 0.00) for marker D2S292. By testing additional markers, the disease gene was localized to a 14.9 cM region on chromosome 2p. University of Oxford Wellcome Trust Centre Bioinformatics Home Publications

31. ScienceDaily News Release: Alstrom Syndrome Genetics Studied At Jackson Laborato Source Jackson Laboratory. Date 199807-20. alstrom syndrome GeneticsStudied At Jackson Laboratory. Bar Harbor Scientists at http://www.sciencedaily.com/releases/1998/07/980720081033.htm

Search Our Archives Keywords: Order by: date relevance More options Get ad-free access with email updates sign up or log in Text size: A A A Welcome Home page About this site Awards, reviews News Summaries Headlines Topics Shop Our stuff Browse books Magazines Software Contribute Register free Post release Edit profile Review hits Advertise Media kit Traffic stats Contact us Previous Story ... Related Stories Next Story Source: Jackson Laboratory Date: Alstrom Syndrome Genetics Studied At Jackson Laboratory Bar Harbor Scientists at The Jackson Laboratory are working towards identifying the gene that causes Alström Syndrome. The research is providing increased understanding of the genetic basis for the disease and may offer fundamental insights into the underlying causes of obesity, diabetes, and sensory defects in humans. As part of the research effort, 46 living Alström individuals have been located in 10 countries, including the U.S. and Canada. Many of those individuals will be attending the Second International Alström Syndrome Gathering, sponsored by the Society for Alström Syndrome Families, July 17-21 in San Luis Obispo, Calif. The first Alström gathering was in Yarmouth, Nova Scotia, in 1995, when only nine individuals were known. The rare inherited syndrome, first described in 1959 by Swedish physician C.H. Alström, is a disease of the young, causing progressively severe conditions such as blindness, hearing loss, kidney disease, scoliosis, obesity, heart disease, and non-insulin-dependent (type 2) diabetes. There is no known cure.

32. ThirdAge - Adam - Alstrom Syndrome alstrom syndrome. Definition Alternative Names AlstromHallgren syndrome; Alstroem'sretino-otodiabetic syndrome. Causes, incidence, and risk factors http://www.thirdage.com/health/adam/ency/article/001665.htm

document.write(''); document.write(''); document.write('<'); document.write('/SCRIPT>'); document.write(''); document.write(''); document.write('<'); document.write('/A>'); document.write('<'); document.write('/NOSCRIPT>'); document.write('<'); document.write('/IFRAME>'); Activities Computers Family Tree Health ... Prevention Alstrom syndrome Definition: an inherited disease characterized by progressive blindness juvenile onset diabetes mellitus, obesity deafness , and normal mental capacity. Alternative Names: Alstrom-Hallgren syndrome; Alstroem's retino-otodiabetic syndrome Causes, incidence, and risk factors: This is an autosomal recessive , inherited disorder. It is extremely rare. The syndrome has a higher incidence in Holland and Sweden. Review Date: 6/16/2001 Reviewed By: Elizabeth Hait, M.D., Department of Pediatrics, Rainbow Babies and Children¹s Hospital, Case Western Reserve University, Cleveland, OH. Review provided by VeriMed Healthcare Network. TOP CLICKS Memory Loss Smallpox Flu Shot Anthrax ... Depression document.write(''); document.write(''); document.write('<'); document.write('/SCRIPT>'); document.write(''); document.write(''); document.write('<'); document.write('/A>'); document.write('<'); document.write('/NOSCRIPT>'); document.write('<'); document.write('/IFRAME>'); THIS WEEK'S FEATURES Make every day like a spa visit Get your over-eating in control with this weight loss menu 5 smart bone-builders that can combat osteoporosis FREE NEWSLETTER Health See latest More Newsletters 2 Years FREE! That's DOUBLE Our Best Offer Ever!

33. Fund-raiser To Assist Youngster Afflicted With Extremely Rare Alstrom Syndrome Fundraiser to assist youngster afflicted with extremely rare alstrom syndrome. (Doctors)recently discovered the gene for alstrom syndrome,' said Bates. http://www.westernwheel.com/010711/news-alstrom.html

return to current issue Wednesday, July 11, 2001 Fund-raiser to assist youngster afflicted with extremely rare Alstrom Syndrome By Gillian Beckett Staff Reporter Notification Would you like to be notified when the Western Wheel is updated each week? first last email On a warm, sunny afternoon, three-year-old Kiefer Bates is enjoying a popsicle on the deck of his house in Turner Valley. Kiefer has Alstrom Syndrome and is the first child in Alberta diagnosed with the disease and the second child in western Canada who is afflicted. Currently, there are only 138 individuals in the world who have the disease. Alstrom Syndrome is a life-threatening, genetic disease which usually strikes in early childhood. The disease is accompanied by retinal degeneration which can lead to blindness, hearing loss, obesity, rapid-eye shifting, photophobia (hyper-sensitivity to light) and Type II Diabetes mellitus. Alstrom Syndrome can also lead to hypothyroidism, liver dysfunction, scoliosis, heart disease and heart failure in infancy or early childhood. 'I started searching for answers when he was two months old,' said Bates. 'We took him to specialists and hospitals in Edmonton, Red Deer and Calgary.'

34. Analysis Of Alstrom Syndrome Analysis of alstrom syndrome, G2D Home. GO TO CHROMOSOMAL REGION Disease mappedalstrom syndrome Chromosome 2 Genomic position startstop 66500000-76500001 http://www.bork.embl-heidelberg.de/g2d/exam_disease.pl?U7840

35. Health Library ALS (Lou Gehrig's Disease). alstrom syndrome InternationalAlstrom's Syndrome. Alstrom'sSyndrome. Alternative Gifts International-Charity / Service Organizations. http://yalenewhavenhealth.org/Library/HealthGuide/SelfHelp/_SearchResults.asp?le

36. Health Library ALS (Lou Gehrig's Disease). alstrom syndrome InternationalAlstrom's Syndrome. Alstrom'sSyndrome. Alt.Support.Shyness.FAQ-Anxiety Attacks / Phobias / Agoraphobia. http://hvelink.saint-lukes.org/library/healthguide/SelfHelp/_SearchResults.asp?l

37. Syndrome alstrom syndrome Support Group UK, This Web site provides information on what AlstromSyndrome is, the clinical features, a newsletter and current research. http://omni.ac.uk/browse/mesh/detail/C0039082L0039082.html

Syndrome [up] Related topics: broader Disease Alstrom Syndrome Support Group - UK Alstrom Syndrome is a very rare condition, with symptoms including childhood blindness, early hearing loss, diabetes, cardiomyopathy and kidney failure. The Alstrom Syndrome Support Group aims to alleviate suffering, and provide support for those with Alstrom Syndrome, and raise public awareness. This Web site provides information on what Alstrom Syndrome is, the clinical features, a newsletter and current research. A discussion list for anyone with an interest in this topic is also available, which aims to enable clinicians, carer and sufferers to share experiences. Charities Genetic Diseases, Inborn Syndrome GeneReviews : 22q11 deletion syndrome Notes for physicians on 22q11 Deletion Syndrome (Shprintzen Syndrome, DiGeorge Syndrome (DGS), Velocardiofacial Syndrome (VCFS), Conotruncal Anomaly Face Syndrome (CTAF), Caylor Cardiofacial Syndrome, Opitz G/BBB) covering diagnosis, clinical description, differential diagnosis, management, molecular genetics and genetic counselling. Revised during September 1999. This resource forms part of GeneReviews (formerly GeneClinics profile), an expert-authored, peer-reviewed medical knowledge base being developed at the University of Washington.This resource contains a summary and bibliographical references of the review, free access to the full-text version of the review requires brief registration. Chromosomes, Human, Pair 22

38. Med Help International A-Z Health Topic Listing loss)(174); Alport Syndrome(1); ALS (Amyotrophic Lateral Sclerosis,Lou Gehrig)(342); alstrom syndrome(1); Alternating Hemiplegia of http://www.medhelp.org/HealthTopics/A.html

[Health Topics A-Z] A B C D ... [Patient Network] Revised: 3/30/2003

39. Alstrom Start Omhoog. Alstrom ENG. alstrom syndrome (3); alstrom syndromeUK Support Group Home Pag; alstrom syndrome; Department of Pharmacy http://www.xs4all.nl/~ritanila/alstrom.html

Alstrom ENG Alstrom syndrome (3) Alstrom Syndrome UK Support Group - Home Pag Alstrom Syndrome Department of Pharmacy, King's College London ... Rare Disorders Alliance - UK

40. Alstrom alstrom syndrome. (See also DIABETES MELLITUS, KIDNEY DISEASE, RETINITIS PIGMENTOSA).alstrom syndrome Newsletter,. 1006 Howard Rd.,. Warminster, PA 18974. http://www.childhealthinfo.com/alstrom-syndrome.htm

ALSTROM SYNDROME (See also DIABETES MELLITUS, KIDNEY DISEASE, RETINITIS PIGMENTOSA) Alstrom Syndrome Newsletter, 1006 Howard Rd., Warminster, PA 18974 [Home] [Printed Guide] [Child Care for the '90's] [Links] ... MoreInfo@ChildHealthInfo.com

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