41. Analysis Of Alstrom Syndrome The number indicates the strength of association to alstrom syndrome . The pointsto the related MeSHD terms. Follow the green arrows to navigate MeSH-C http://www.bork.embl-heidelberg.de/g2d/exam_disease.pl?U7840

42. References For Alstrom Syndrome With The MeSH Term Retinal References for alstrom syndrome with the MeSH term Retinal Degeneration, G2D Home.PMID and date. Follow the link to see the corresponding entry by PubMed http://www.bork.embl-heidelberg.de/g2d/exam_mesh_disease.pl?Retinal_Degeneration

43. Type 2 Diabetes In Alstrom Syndrome: Targeting Insulin Resistance With A Thiazol alstrom syndrome is an autosomal recessive disorder characterised by obesity,sensorineural deafness, conerod dystrophy and hypergonadotrophic hypogonadism http://www.endocrine-abstracts.org/ea/0005/ea0005p104.htm

Endocrine Abstracts previous abstract next abstract Abstract Type 2 diabetes in Alstrom syndrome: Targeting insulin resistance with a thiazolidinedione S Nag , WF Kelly , M Walker Department of Diabetes and Endocrinology, James Cook University Hospital, Middlesbrough, UK; Department of Diabetes and Metabolism, University of Newcastle, Newcastle upon Tyne, UK. Alstrom syndrome is an autosomal recessive disorder characterised by obesity, sensorineural deafness, cone-rod dystrophy and hypergonadotrophic hypogonadism. Diabetes in these patients is characterised by severe insulin resistance. We describe the management of diabetes in a 28 year old male patient with Alstrom syndrome and severe insulin resistance. Obesity developed early in childhood and at 3 years weight was 22.2 kg. Genetic studies revealed that the patient is a compound heterozygote, with a frameshift mutation and translocation break point in the paternal and maternal alleles, respectively of the ALMS1 gene. Diabetes was diagnosed at age 14. Islet cell antibodies were negative. Peripheral insulin resistance was assessed by the hyperinsulinaemic isoglycaemic clamp technique.Insulin sensitivity, expressed as the glucose infusion rate [M value] was 48mg/m /min.Mean M values for a similar group of moderately obese subjects was 80 mg/m

44. Alstrom Syndrome: Confirmation Of Linkage To Chromosome 2p12-13 And Phenotypic H Charles SJ, Moore AT, Yates JRW, Green T, Clark P. Alstrom s syndrome furtherevidence alstrom syndrome a case misdiagnosed as BardetBiedl syndrome. http://jmg.bmjjournals.com/cgi/content/full/37/7/e8

HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS Author Keyword(s) Vol Page [Advanced] This Article Extract Full Text (PDF) Submit a response ... Citation Map Services Email this link to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Download to citation manager PubMed PubMed Citation Articles by ZUMSTEG, U. Articles by MISEREZ, A. R Related Collections Genetics J Med Genet e8 ( July ) Electronic letters E DITOR et al in 1959 as a combination of atypical retinal degeneration, obesity, diabetes mellitus, and neurogenic deafness. Since this first report, further features of the syndrome have been described, including hypertriglyceridaemia, hepatic dysfunction, hyperuricaemia, slowly progressive chronic nephropathy, hypothyroidism, male hypogonadism, androgenetic alopecia, growth retardation

45. Alstrom's Syndrome: Further Evidence Of Autosomal Recessive Inheritance And Endo We report a case of Alstrom s syndrome with hypothyroidism in addition to the alstrom syndrome confirmation of linkage to chromosome 2p1213 and http://jmg.bmjjournals.com/cgi/content/abstract/27/9/590

HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS Author Keyword(s) Vol Page [Advanced] This Article Submit a response Alert me when this article is cited Alert me when eLetters are posted Alert me if a correction is posted Services Email this link to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Cited by other online articles PubMed PubMed Citation Articles by Charles, S. J. Articles by Clark, P. Journal of Medical Genetics, 1990, Vol 27, 590-592 ARTICLES Alstrom's syndrome: further evidence of autosomal recessive inheritance and endocrinological dysfunction SJ Charles, AT Moore, JR Yates, T Green and P Clark Department of Ophthalmology, Addenbrooke's Hospital, Cambridge. We report a case of Alstrom's syndrome with hypothyroidism in addition to the cardinal features of blindness, deafness, obesity, and insulin

46. Geneticalliance.org alstrom syndrome Support Groups Alstršm Syndrome International 14 WhitneyFarm Road Mt. Desert, ME 4660 Phone 207.244.7043 Fax 207.288.6078 http://www.geneticalliance.org/ws_display.asp?filter=support_groups_by_disease&t

47. GEMdatabase - Selected Title TITLE, alstrom syndrome. DESCRIPTION, This review focuses on the diagnosis,management, and genetic counseling of patients and families with Alström http://www.gemdatabase.org/GEMDatabase/TitleDetailsOne.asp?TitleID=825

48. Arch Intern Med -- Abstract: New Alstrom Syndrome Phenotypes Based On The Evalua New Alström Syndrome Phenotypes Based on the Evaluation of 182 Cases Background Alström syndrome is a recessively inherited genetic disorder http://archinte.ama-assn.org/cgi/content/abstract/165/6/675

Select Journal or Resource JAMA Archives of Dermatology Facial Plastic Surgery Family Medicine (1992-2000) General Psychiatry Internal Medicine Neurology Ophthalmology Surgery Student JAMA (1998-2004) JAMA CareerNet For The Media Meetings Peer Review Congress Vol. 165 No. 6, March 28, 2005 Featured Link E-mail Alerts Original Investigation Article Options Full text PDF Send to a Friend Similar articles in this journal Literature Track Add to File Drawer Download to Citation Manager PubMed citation Articles in PubMed by Marshall JD Nishina PM Articles that cite this article Contact me when this article is cited Topic Collections Genetics Genetic Disorders Topic Collection Alerts Jan D. Marshall, BA Roderick T. Bronson, DVM Gayle B. Collin, MS Anne D. Nordstrom, PhD Pietro Maffei, MD, PhD Richard B. Paisey, MD Catherine Carey, MD Seamus MacDermott, MD Isabelle Russell-Eggitt, MD Sarah E. Shea, MD Judy Davis, MD Sebastian Beck, MD, PhD Gocha Shatirishvili, MD Cristina Maria Mihai, MD Maria Hoeltzenbein, MD Giovanni Battista Pozzan, MD Ian Hopkinson, MD, PhD

49. Alstrom Syndrome alstrom syndrome. Use. genetic disorder. Use. retinitis pigmentosa. Use.syndrome. Send your comments to MultiTes. http://crisp.cit.nih.gov/Thesaurus/00018706.htm

Prev Term: alstonia Next Term: Alternaria Alstrom syndrome Use: genetic disorder Use: retinitis pigmentosa Use: syndrome Send your comments to: Melody Lowe

50. Alström Syndrome - Genetics Home Reference What other names do people use for Alström syndrome? AlstromHallgren syndrome;alstrom syndrome. See How are genetic conditions and genes named? in the http://ghr.nlm.nih.gov/condition=alstromsyndrome

Home What's New Browse Handbook ... Related Gene(s) Quick links to this topic MedlinePlus Health Information Educational resources Information pages Patient support For patients and families Gene Reviews Clinical summary Gene Tests DNA test labs PubMed Recent literature OMIM Genetic disorder catalog References On this page: What is How common What genes How do people ... glossary definitions This condition is rare; only about 300 people are known to be affected worldwide. Mutations in the MedlinePlus - Health Information (5 links) Educational resources - Information pages (2 links) Patient support - For patients and families (2 links) You may also be interested in these resources, which are designed for healthcare professionals and researchers. Gene Reviews - Clinical summary Gene Tests - DNA tests ordered by healthcare professionals PubMed - Recent literature OMIM - Genetic disorder catalog Alstrom-Hallgren syndrome Alstrom syndrome See How are genetic conditions and genes named? in the Handbook. See How can I find a genetics professional in my area? in the Handbook. Ask the Genetic and Rare Diseases Information Center Where can I find general information about genetic conditions?

51. 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

52. Surgery Door - Support Groups alstrom syndrome UK was set up by two parents of affected children. The groupcombines its aim to reach all affected families in the UK with its desire for http://www.surgerydoor.co.uk/sg/detail.asp?Recno=26740358

53. Rare Diseases Terms - Office Of Rare Diseases Additional information about alstrom syndrome is available from.http//ghr.nlm.nih.gov/condition=alstromsyndrome. Last Reviewed Wednesday, June08, 2005 http://ord.aspensys.com/asp/diseases/diseaseinfo.asp?ID=5787

54. Conditions And Diseases/Rare Disorders/Alstrom Syndrome Conditions and Diseases/Rare Disorders/alstrom syndrome healthboard. http://www.healthboard.com/websites/Conditions_and_Diseases/Rare_Disorders/Alstr

Health Board Conditions and Diseases/Rare Disorders/Alstrom Syndrome Search Health Board Directories the entire directory only this category More search options Home Conditions and Diseases Rare Disorders : Alstrom Syndrome LINKS: Alstrom Syndrome Clinical features, literature and research. Includes guidelines for health care professionals. http://www.jax.org/alstrom Alstrom Syndrome of Canada Includes information about the condition, and the organisation. http://alstromsyndrome.ca Alstrom Syndrome UK Support Group Information centre and discussion forum for anyone with an interest in this disorder. http://www.alstrom.org.uk/ NORD - Alstrom Syndrome Sample report, plus links to organisations. [Fee required for full report] http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Alstrom%20Syndrome Smart Groups: Alstr¶m Families Mailing list, pictures, links and files. http://smartgroups.com/groups/alstromfamilies HOME NEW LINKS COOL LINKS NEWSLETTER ... HealthBoard.com

55. XM_355793 [Alms1] - Alstrom Syndrome 1 Homolog (human) @ Brain Gene Expression M Brain Gene Expression Map for alstrom syndrome 1 homolog (human). This is partof the Brain Gene Expression Map Project hosted at http//www.stjudebgem.org. http://www.stjudebgem.org/web/view/probe/viewProbeDetails.php?id=2319

56. The American Journal Of The Medical Sciences - UserLogin alstrom syndrome (ALMS) is a very rare genetic autosomal recessive Alstromsyndrome is a rare disease that is due to a Mendelian recessive trait, http://www.amjmedsci.com/pt/re/ajms/fulltext.00000441-200405000-00031.htm

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57. Gene Official Symbol ALMS1 and Name alstrom syndrome 1 provided by HUGO Gene Mutations in this gene have been associated with alstrom syndrome. http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=gene&cmd=Retrieve&dopt=Graphics

58. OMIM - ALSTROM SYNDROME; ALMS http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=203800

59. Alstrom alstrom syndrome (3) alstrom syndrome UK Support Group Home Pag EasternOphthalmic Pathology Society 1983 Index Family Village- alstrom syndrome http://www.xs4all.nl/~ritanila/alstrom.html

Alstrom ENG Alstrom syndrome (3) Alstrom Syndrome UK Support Group - Home Pag Eastern Ophthalmic Pathology Society 1983 Index Family Village- Alstrom Syndrome ... Rare Disorders Alliance - UK

60. Rarest Illnesses Vex Parents - 07/01/04 With only 10 families in Canada affected by alstrom syndrome, there is littlechance they can solve many of the problems that face people with rare http://www.detnews.com/2004/health/0407/01/a10-200330.htm

@import url(/includes/css/enhanced.css); Latest Health reports Home Page Essentials CyberSurveys Forums Photo Galleries Weather ... Contact Us Autos Autos Insider Drive New Car Photos Car Reviews ... Joyrides Business Business Careers Find a Job Real Estate ... Find a Home Metro Metro/State Wayne Oakland Macomb ... Detroit History Nation/World Nation/World Politics/Gov Census Health ... Technology Sports Sports Insider LIons/NFL Pistons/NBA Red Wings/NHL ... Scoreboards Entertainment Entertainment Rant/Rave Events Event Finder ... Michigan's Best Living Lifestyle Homestyle Fitness Forums News Talk Faith Talk Autos Talk Wings Talk ... Tech Talk Weblogs Photo Blog Politics Blog Pistons Blog Tigers Blog ... Entertainment RSS Feeds Previous Story Next Story Thursday, July 1, 2004 Rarest illnesses vex parents They often must teach doctors about their children's diseases By Anne McIlroy / Toronto Globe and Mail Comment on this story Send this story to a friend Get Home Delivery TORONTO — Eight-year-old Palmer Douglas was a toddler when he was diagnosed with a life-threatening disorder so rare that only about 250 cases have been identified worldwide. Against unbelievable odds, both his parents, Randy and Kim, carry a copy of an extremely rare recessive gene that causes Alstrom syndrome. Palmer inherited both copies, and as a result he is prone to obesity and susceptible to diabetes, heart and kidney failure and liver disease. Some with this disease die in their teens or early adulthood; most progressively lose their vision throughout their childhood.

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