21. Laurence-Moon Syndrome - Definition Of Laurence-Moon Syndrome In The Medical Dic Definition of laurencemoon syndrome in the Medical Dictionary and Thesaurus.laurence-moon syndrome explanation. Information about laurence-moon syndrome http://medical-dictionary.thefreedictionary.com/Laurence-Moon syndrome

Domain='thefreedictionary.com' word='Laurence-Moon syndrome' Your help is needed: American Red Cross The Salvation Army join mailing list webmaster tools Word (phrase): Word Starts with Ends with Definition subscription: Dictionary/ thesaurus Computing dictionary Medical dictionary Legal dictionary Financial dictionary Acronyms Columbia encyclopedia Wikipedia encyclopedia Hutchinson encyclopedia Laurence-Moon syndrome 0.02 sec. Page tools Printer friendly Cite / link Email Feedback Laurence-Moon syndrome n. An inherited syndrome attributed to recessive mutations of two genes on the same chromosome and characterized by mental retardation, pigmentary retinopathy, hypogenitalism, and spastic paraplegia. Mentioned in Laurence-Moon-Bardet-Biedl syndrome Medical browser Full browser latissimus dorsi Latrodectus LATS latus ... laughing gas Laurence-Moon syndrome Laurence-Moon-Bardet-Biedl syndrome lauric acid lauryl alcohol lavage ... Laurence, Saint Laurence-Moon syndrome Laurence-Moon-Bardet-Biedl syndrome Laurence-Moon-Biedl syndrome Laurence-Moon-Biedl syndrome Laurence-Moon-Biedl-Bardet syndrome ... Laurens County Word (phrase): Word Starts with Ends with Definition Free Tools: For surfers: Browser extension Word of the Day NEW!

22. Penn State Faculty Research Expertise Database (FRED) , An autosomal recessive condition This syndrome was previously referred to as Laurence-Moon-Biedl syndrome until......laurencemoon syndrome. http://fred.hmc.psu.edu/ds/retrieve/fred/meshdescriptor/D007849

23. National Neurovision Research Institute Click Here For More BardetBiedl syndrome is often confused with laurence-moon syndrome. laurence-moon syndrome is extremely rare; only a few cases have been documented. http://www.blindness.org/visiondisorders/causes.asp?type=27

24. Health/Conditions And Diseases/Genetic Disorders/Laurence-Moon Syndrome -- The D NORD Laurence Moon Syndrome Offers alternative names, a general discussion and A definition of laurencemoon syndrome followed by the epidemiology, http://www.thedoctorslounge.net/dir/Health/Conditions_and_Diseases/Genetic_Disor

Advertisement Powered by Careerbuilder Search for: Home Humor Advertising Contact ... Links Specialties Cardiology Chest diseases Dermatology Endocrinology ... Urology Other Sections Membership Research Tools Medical Tutorials Medical Software ... Specialized Centers Headlines: The Medical Website Directory Popular Categories Popular Links Web Sites Laurence Moon Bardet Biedl Society Fully accessible site for people with LMBB, their families, friends, carers and interested professionals. Opinions, news, views, research, updates, and contact details. url: www.lmbbs.org.uk National Library of Medicine: Laurence-Moon Syndrome A look at its former names, a summary and a list of clinical features. url: www.nlm.nih.gov/cgi/jablonski/syndrome_cgi?term=La... NORD: Laurence Moon Syndrome Offers alternative names, a general discussion and further resources. url: www.rarediseases.org/search/rdbdetail_abstract.htm... Pediatric Database A definition of Laurence-Moon syndrome followed by the epidemiology, pathogenesis, clinical features, investigations and management. url: www.icondata.com/health/pedbase/files/LAURENCE.HTM

25. Bardet-Biedl Syndrome - The Foundation Fighting Blindness - Canada LaurenceMoon-Biedl syndrome is also known as laurence-moon syndrome. In individualswith laurence-moon syndrome related neurological problems, http://www.ffb.ca/disease_bardet-biedl-txt.html

26. A Retinal Disease With Systemic Associations -- Answer Medscape, www.medscape.com. B) laurencemoon syndrome is incorrect. Try again http://www.medscape.com/content/2004/00/47/91/479108/ans2.html

B) Laurence-Moon syndrome is incorrect. Try again...

27. Log In Problems 17 As opposed to BardetBiedl syndrome, laurence-moon syndrome is associated 17 Additionally, the pigmentary retinopathy of laurence-moon syndrome http://www.medscape.com/viewarticle/479108_print

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28. Retina Association Of New Zealand: Diseases Section - Bardet-Beidl Syndrome BardetBiedl syndrome is often confused with laurence-moon syndrome. laurence-moon syndrome is extremely rare; only a few case have been documented. http://www.retina.org.nz/diseases/bardet.htm

INFORMATION ABOUT BARDET-BIEDL SYNDROME Information courtesy of "The Foundation for Fighting Blindness" Bardet-Biedl syndrome is a complex disorder that affects many parts of the body including the retina. Individuals with this syndrome have a retinal degeneration similar to retinitis pigmentosa (RP). Clinical description The diagnosis of Bardet-Biedl syndrome is usually confirmed in childhood when visual problems due to RP are discovered. The first symptom of RP is night blindness. Night blindness makes it difficult to see in low light levels. RP then causes progressive loss of peripheral (side) vision. Peripheral vision loss is often referred to as tunnel vision. Individuals with Bardet-Biedl also experience central vision loss during childhood or adolescence. RP symptoms progress rapidly and usually lead to severe visual impairment by early adulthood. In addition to RP, polydactyly (extra fingers and/or toes) and obesity are defining characteristics of Bardet-Biedl syndrome. A diagnosis of Bardet-Biedl syndrome is usually first suspected when a child is born with polydactyly.

29. Laurence-Moon-Biedl Syndrome CAUSES. genetic. Synonyms. laurencemoon syndrome; Bardet-Biedl syndrome.ICD-9-CM 759.89 Other specified anomalies (Laurence-Moon-Biedl syndrome) http://www.5mcc.com/Assets/SUMMARY/TP0519.html

Laurence-Moon-Biedl syndrome DESCRIPTION: A hereditary syndrome of childhood, transmitted as an autosomal recessive trait, with obesity, retinitis pigmentosa, mental retardation, polydactyly, and hypogonadism as the main features. Usual course - progressive. CAUSES: genetic Synonyms: Laurence-Moon syndrome Bardet-Biedl syndrome ICD-9-CM: 759.89 Other specified anomalies (Laurence-Moon-Biedl syndrome) Author(s): Mark R. Dambro, MD

30. Laurence-Moon Syndrome laurencemoon syndrome Medical.WebEnds.com. Laurence-Moon-Biedl Syndrome;Laurence Moon Biedl Syndrome; Laurence Moon Syndrome; Syndrome, Laurence-Moon; http://medical.webends.com/kw/Laurence-Moon Syndrome

Medical.WebEnds.com - Medical Terminology Dictionary A B C D ... Z WWW Medical.WebEnds.com Laurence-Moon Syndrome Laurence-Moon-Biedl Syndrome; Laurence Moon Biedl Syndrome; Laurence Moon Syndrome; Syndrome, Laurence-Moon; Syndrome, Laurence-Moon-Biedl An autosomal recessive condition characterized by hypogonadism ; spinocerebellar degeneration; MENTAL RETARDATION RETINITIS PIGMENTOSA; and OBESITY . This syndrome was previously referred to as Laurence- Moon -Biedl syndrome until BARDET-BIEDL SYNDROME was identified as a distinct entity. (From N Engl J Med. 1989 Oct 12;321(15):1002-9) Google links Processing time was 0.034026145935059 seconds.

31. MeSH-D Terms Associated To MeSH-C Term Laurence-Moon Syndrome MeSHD terms associated to MeSH-C term laurence-moon syndrome, G2D Home strength of the association of the corresponding term to laurence-moon syndrome. http://www.bork.embl-heidelberg.de/g2d/c2d.pl?Laurence-Moon_Syndrome:benchmark

32. Opera Directory National Library of Medicine laurencemoon syndrome NORD Laurence MoonSyndrome. Offers alternative names, a general discussion and further resources. http://portal.opera.com/directory/?cat=525030

33. Débats Listesnof : Syndrome De Laurence-Moon-Bardet-Biedl Translate this page 3) Laurence Moon (syndrome de) MIM*245800 Autosomique récessif Retard mental, The laurence-moon syndrome (strictu sensu) is the same as the disorder http://g5d.chez.tiscali.fr/COCNet10/COCMED10/lsnofLBB.htm

sommaire Syndrome de Laurence-Moon-Bardet-Biedl Chers Amis Un conseil : http://www.healthgate.com/HealthGate/home.html Yannick LE MER Amicalement Chantal NOVEL Xavier ZANLONGHI Voir E.M.C. Ophtalmologie 21470 A 50, Les syndromes oculo-auditifs, page 12 Cordialement Georges LAROCHE Marc Abitbol avait fait une remarquable mise au point sur ces syndromes. Pourrait-il nous la redonner? ou notre webmaster? Alain BRON *209900 BARDET- BIEDL SYNDROME, TEXT This condition is characterized by mental retardation, pigmentary retinopathy, polydactyly, obesity, and hypogenitalism, and has incorrectly been called LMBB (Laurence-Moon-Bardet-Biedl) syndrome. Ammann (1970) pointed out that these features were present in the patients of Biedl (1922) and Bardet (1920), but that the patients of Laurence and Moon had a distinct disorder with paraplegia and without polydactyly and obesity (see Laurence-Moon syndrome, 245800). As indicated by Ammann's study, residual heterogeneity may exist even after the Laurence-Moon syndrome is separated. In Bedouin families in the Negev region of Israel, presumably the same kindreds as those studied by Kwitek-Black et al. (1993), Elbedour et al. (1994) performed echocardiographic evaluations of cardiac involvement in BBS. They stated that they found cardiac involvement in 50% of cases, justifying inclusion of echocardiographic examination in the clinical evaluation and follow-up of these patients. However, their table 1 gives echocardiographic abnormality in only 7 of 22 cases and these included 1 case of bicuspid aortic valve, 1 case of mild thickening of the interventricular septum, 1 case of 'moderate tricuspid regurgitation,' and 1 case of mild pulmonic valve stenosis. The occurrence of renal abnormality in 11 of the 22 patients on kidney ultrasonography was somewhat more impressive than the cardiac involvement.

34. 245800 LAURENCE-MOON SYNDROME that of 2 patients clinically diagnosed as having laurencemoon syndrome, not support the notion that BBS and laurence-moon syndrome are distinct. http://srs.sanger.ac.uk/srsbin/cgi-bin/wgetz?[omim-ID:245800] -e

35. 604896.0008 BARDET-BIEDL SYNDROME 6 MKKS, LEU277PRO (2005) as having been clinically diagnosed with laurencemoon syndrome (245800).Moore et al. (2005) considered their identification of mutations in the http://srs.sanger.ac.uk/srsbin/cgi-bin/wgetz?-e [omim_allele-id:604896_8]

36. The Health Library — Genetics And Birth Defects DeafnessDystonia-Optic Neuronopathy Syndrome (DFN-1, Mohr-Tranebjaerg Syndrome) laurence-moon syndrome. Laurence Moon SyndromeNORD http://healthlibrary.stanford.edu/resources/internet/bodysystems/genetic_mca_dm.

Diseases and Disorders Use these links to jump directly to your topic of interest in Genetics and Birth Defects: Genetics: General Genetics Gene Therapy Genetic Counseling Genetic Testing ... Genetics of Specific Diseases Birth Defects: General Birth Defects Cardiovascular Defects Connective Tissue Disorders Craniofacial Anomalies ... S - W Multiple Congenital Anomalies (D - M) Jump to: A B C D ... P Q R S T U ... W X Y Z Deafness-Dystonia-Optic Neuronopathy Syndrome (DFN-1, Mohr-Tranebjaerg Syndrome) Deafness-Dystonia-Optic Neuronopathy Syndrome:GeneReviews Down Syndrome Down Syndrome:March of Dimes Facts About Down Syndrome:NICHD Down Syndrome (Trisomy 21):Lucile Packard Children's Hospital Information and Resources:National Down Syndrome Society ... Let's Talk About Down Syndrome:netLibrary for Kids] Everything You Need to Know About Down Syndrome:netLibrary [for Teens] Down Syndrome : A Promising Future, Together:netLibrary Down Syndrome:Genetics Home Reference, NLM Down Syndrome:Society for Neuroscience Down Syndrome:MedlinePlus Dyskeratosis Congenita Dyskeratosis Congenita:Madisons Foundation Dyskeratosis Congenita:eMedicine Dyskeratosis Congenita:National Cancer Institute Ectodermal Dysplasia Ectodermal Dysplasia (EDS):U.C. Davis Children's Hospital

37. Optometry And Vision Science - UserLogin The historically associated laurencemoon syndrome includes spastic It isbelieved that in the laurence-moon syndrome, polydactyly and obesity are not http://www.optvissci.com/pt/re/ovs/fulltext.00006324-200005000-00010.htm

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38. Optometry And Vision Science - Abstract: Volume 77(5) May 2000 P 236-243 Bardet- Cognitive deficit has also been considered part of the syndrome. The historicallyassociated laurencemoon syndrome includes spastic paraparesis but not the http://www.optvissci.com/pt/re/ovs/abstract.00006324-200005000-00010.htm

LWWOnline LOGIN eALERTS REGISTER ... Archive Bardet-Biedl Syndrome. ARTICLE LINKS: Fulltext PDF (434 K) Bardet-Biedl Syndrome. Hrynchak, Patricia K. OD, FAAO Abstract: (C) 2000 American Academy of Optometry Subscribe to RSS feed utrdc-pt01 Release 4.0

39. Topic And Category Listing Lateral Medullary Syndrome. Lateral Medullary Syndrome. Lateral Sinus Thrombosis laurencemoon syndrome. laurence-moon syndrome. Back to top ^ http://search.dartmouth-hitchcock.org/dhmc/servlet/submit?Pg=Topic&Tp=L&visit=1

40. Birth Defect: Definition And Much More From Answers.com Incontinentia Pigmenti; Ivemark syndrome; Jacobsen syndrome KarschNeugebauersyndrome Klinefelter syndrome; Larsen syndrome; laurence-moon syndrome http://www.answers.com/topic/congenital-disorder

showHide_TellMeAbout2('false'); Business Entertainment Games Health ... More... On this page: Dictionary Diagnosis Encyclopedia Medical WordNet Wikipedia Best of Web Mentioned In Or search: - The Web - Images - News - Blogs - Shopping birth defect Dictionary birth defect n. A physiological or structural abnormality that develops at or before birth and is present at the time of birth, especially as a result of faulty development, infection, heredity, or injury. Also called congenital anomaly Diagnosis Birth Defects All parents are at risk of having a baby with a birth defect, regardless of age, race, income or residence. Parents of children with birth defects are very much encouraged to discuss the specifics of the defect on their child's current condition and the risks, if any, for future children. Related Links on MedicineNet.com Page 2 of this Article Related Medical Procedures and Tests The Doctor's Response Information on this web site is provided for informational purposes only and is not a substitute for professional medical advice. You should not use the information on this web site for diagnosing or treating a medical or health condition. You should carefully read all product packaging. If you have or suspect you have a medical problem, promptly contact your professional healthcare provider. Statements and information regarding dietary supplements have not been evaluated or approved by the Food and Drug Administration. Please consult your healthcare provider before beginning any course of supplementation or treatment.

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