The Health Library Genetics And Birth Defects alstrom syndrome. alstrom syndromeMedlinePlus Medical Encyclopedia. alstrom syndromealstrom syndrome International. alstrom syndromeGeneReviews. http://healthlibrary.stanford.edu/resources/internet/bodysystems/genetics6.html
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Extractions: 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
Health - Conditions And Diseases - Rare Disorders - Alstrom Top Health Conditions and Diseases Rare Disorders alstrom syndrome Attention webmaster Error reading data from dmoz! Make sure the dmoz url is correct. http://www.sedirectory.net/Health/Conditions_and_Diseases/Rare_Disorders/Alstrom
Extractions: Web Hosting Dir Web Design Dir Search Engine Dir Hardware Info ... Resources Search: Top Health Conditions and Diseases Rare Disorders ... Alstrom Syndrome See also: Health: Conditions and Diseases: Genetic Disorders Alstr¶m Syndrome - Clinical features, literature and research. Includes guidelines for health care professionals. Alstr¶m Syndrome of Canada - Includes information about the condition, and the organisation. Alstr¶m Syndrome UK Support Group - Information centre and discussion forum for anyone with an interest in this disorder. NORD - Alstr¶m Syndrome - Sample report, plus links to organisations. [Fee required for full report] Smart Groups: Alstr¶m Families - Mailing list, pictures, links and files.
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 Web directory and search engine. A reliable source of quality information and web links for alstrom syndrome. SurfRocket.com. alstrom syndrome. http://www.surfrocket.com/Health/Conditions_and_Diseases/Rare_Disorders/Alstrom_
ORPHANET® Alstrom Syndrome Orphanet database access. alstrom syndrome. Direct access to data Summary alstrom syndrome is a rare disorder described in about 80 patients worldwide. http://www.orpha.net/static/GB/alstromsyndrome.html
ORPHANET - Rare Diseases - Orphan Drugs Printing version, DISEASE alstrom syndrome, alstrom syndrome is a rare disorder described in about 80 patients worldwide. It is http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=64
Surgery Door - Support Groups alstrom syndrome UK. 49 Southfield Avenue childhood. alstrom syndrome UK was set up by two parents of affected children. The group http://www.surgerydoor.co.uk/sg/detail.asp?Recno=26740358
Alstrom Syndrome Alstrom ºî¦X¯g The summary for this Chinese (Traditional) page contains characters that cannot be correctly displayed in this language/character set. http://www.kingdoctor.com/cgi-bin/content.asp?id=aza79
Blackwell Synergy - Cookie Absent Natural history of alstrom syndrome in early childhood onset with dilated cardiomyopathy. J Pediatr 1996 128 225229. MEDLINE Abstract ISI Abstract. http://www.blackwell-synergy.com/links/doi/10.1111/j.0009-9163.2004.00204.x/abs/
Extractions: Home An Error Occurred Setting Your User Cookie A cookie is a small amount of information that a web site copies onto your hard drive. Synergy uses cookies to improve performance by remembering that you are logged in when you go from page to page. If the cookie cannot be set correctly, then Synergy cannot determine whether you are logged in and a new session will be created for each page you visit. This slows the system down. Therefore, you must accept the Synergy cookie to use the system. What Gets Stored in a Cookie? Synergy only stores a session ID in the cookie, no other information is captured. In general, only the information that you provide, or the choices you make while visiting a web site, can be stored in a cookie. For example, the site cannot determine your email name unless you choose to type it. Allowing a web site to create a cookie does not give that or any other site access to the rest of your computer, and only the site that created the cookie can read it. Please read our for more information about data collected on this site.
Blackwell Synergy - Cookie Absent Sicolo, N., Martin, M., Nishina, PM Naggert, JK (2002) Mutations in ALMS1 cause obesity, type 2 diabetes and neurosensory degeneration in alstrom syndrome. http://www.blackwell-synergy.com/links/doi/10.1111/j.1365-2265.2004.01952.x/full
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Homozygosity Mapping At Alstrom Syndrome To Chromosome 2p. Homozygosity mapping at alstrom syndrome to chromosome 2p. Collin GB, Marshall JD, Cardon LR and Nishina PM Hum Mol Genet (1997) 6 http://bioinformatics.well.ox.ac.uk/~lon/Pubs/0009063741.html
Extractions: 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
Wauu.DE: Health: Conditions And Diseases: Rare Disorders: Alstrom Syndrome http//smartgroups.com/groups/alstromfamilies. alstrom syndrome Contains information about this syndrome, medical references, International Society for Alstrom http://www.wauu.de/Health/Conditions_and_Diseases/Rare_Disorders/Alstrom_Syndrom
Network Of Care Self Help Clearinghouse. Alstrom s Syndrome. alstrom syndrome International. Back to Top. International Network. 2 affiliated groups (Canada and UK). Founded 1995. http://santabarbara.networkofcare.org/aging/library/hwdetail.cfm?hwid=shc29als&c
Alstrom Syndrome Genetics Studied At Jackson Laboratory alstrom syndrome Genetics Studied At Jackson Laboratory. Bar Harbor Scientists at The Jackson Laboratory are working towards identifying http://www.sciencedaily.com/releases/1998/07/980720081033.htm
Extractions: Source Jackson Laboratory Date Print this page Email to friend 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. Knockout Mouse Reveals Genetic Mechanism In Defective Mammalian Ear Developoment related stories Related section: 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.
Extractions: Front Page Today's Digest Week in Review Email Updates ... Rare Disorders Alstrom Syndrome (5 links) See Also: News about Alstrom Syndrome New Cardiac Arrhythmia Syndrome Identified (June 1, 2004) full story Silence Of The Genes: Researchers Provide Unique View Of Inherited Disorders And Cancer (June 1, 2004) full story UW-Madison Scientists Find A Key To Cell Division (May 28, 2004) full story Vaccines Against Foodborne Disease On Horizon (May 25, 2004) full story Discovery Of Gene For Cornelia De Lange Syndrome Discovery May Lead To Prenatal Test For Debilitating Disorder (May 20, 2004) full story [ More news about Alstrom Syndrome
Alstrom Syndrome From Linkspider UK Health Directory alstrom syndrome by Linkspider UK, alstrom syndrome links and alstrom syndrome topics from our Health directory. Helping you find http://linkspider.co.uk/Health/ConditionsandDiseases/RareDisorders/AlstromSyndro
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