21. Searchalot Directory For Laurence-Moon Syndrome Sponsored Links. Top Health Conditions and Diseases Genetic Disorders LaurenceMoonSyndrome (4). Related Web Sites. http://www.searchalot.com/Top/Health/ConditionsandDiseases/GeneticDisorders/Laur

Home Search News Email Greetings Weather ... Global All the Internet About AltaVista AOL Search Ask Jeeves BBC Search BBC News Business Dictionary Discovery Health Dogpile CheckDomain CNN Corbis eBay Education World Employment Encyclopedia Encarta Excite Fast Search FindLaw FirstGov Google Google Groups Infomine iWon Librarians Index Looksmart Lycos Metacrawler Microsoft Northern Light Open Directory SearchEdu SearchGov Shareware Teoma Thesaurus Thunderstone WayBackMachine Webshots WiseNut Yahoo! Yahoo! Auctions Yahoo! News Yahooligans Zeal Sponsored Links Top Health Conditions and Diseases Genetic Disorders : Laurence-Moon Syndrome Related 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. NORD - Laurence Moon Syndrome - Offers alternative names, a general discussion and further resources. Pediatric Database - A definition of Laurence-Moon syndrome followed by the epidemiology, pathogenesis, clinical features, investigations and management. National Library of Medicine - A look at the former names of Laurence-Moon syndrome, a summary and a list of clinical features.

22. Mioti: Medical Condition Condition Laurence Moon Syndrome. NORD Laurence Moon Syndrome. Information fromthe National Organization for Rare Disorders. OMIM laurencemoon syndrome. http://www.mioti.com/cat/condition/condition.asp?Cat=LaurenceMoon

23. MeSH-D Terms Associated To MeSH-C Term Laurence-Moon Syndrome MeSHD terms associated to MeSH-C term laurence-moon syndrome, G2DHome. The number indicates the strength of the association of the http://www.bork.embl-heidelberg.de/g2d/c2d.pl?Laurence-Moon_Syndrome:unknown

24. Directory :: Look.com laurencemoon syndrome (4) See Also. NORD - Laurence Moon Syndrome Offersalternative names, a general discussion and further resources. http://www.look.com/searchroute/directorysearch.asp?p=525030

25. THE LIGHTNING HYPERTEXT OF DISEASE. Packet No. 4 42373 245800 laurencemoon syndrome, MAPPED, AR Click below to seethe complete OMIM entry for this entity http//www.ncbi.nlm.nih.govhttp//www http://www.pathinfo.com/cgi-bin/lh.cgi?tx=laurence

26. Health Library - Bardet Biedl Syndrome Confusion exists in the medical literature regarding the differencebetween BardetBiedl Syndrome and laurence-moon syndrome. Some http://hvelink.saint-lukes.org/library/healthguide/IllnessConditions/topic.asp?h

27. Health Library - Laurence Moon Syndrome SEARCH. Laurence Moon Syndrome. Confusion exists in the medical literature regardingthe difference between laurencemoon syndrome and Bardet-Biedl Syndrome. http://www.muskogeehealth.com/Library/HealthGuide/IllnessConditions/topic.asp?hw

28. Laurence Moon Biedl Syndrome ? ? ? 245800 laurencemoon syndrome209900 Bardet-Biedl Syndrome, Type 2; BBS2. ? http://ibis-birthdefects.org/start/ukrainian/ulaurenc.htm

Please set browser to encoding in cyrillic) Ïðî I.B.I.S. " íîâèíàõ" Ïðèºäíàéòåñü äî I.B.I.S. Ó 1937 ðîö³, êîëè áóëî âïåðøå îïèñàíî 87 âèïàäê³â öüîãî ñèíäðîìó ó ë³òåðàòóð³, âèÿâëåíî, ùî ëèøå 24 (ïîíàä 28%) ç íèõ ìàëè 5 îñíîâíèõ ðèñ; ðåøòà 63 (72%) áóëè "íåïîâíèìè". Íàçâà ñèíäðîìó ïîõîäèòü â³ä ïð³çâèù àâòîð³â, ÿê³ âïåðøå îïèñàëè éîãî ó ñâî¿õ ïàö³ºíò³â ç íàÿâí³ñòþ ï'ÿòè êàðäèíàëüíèõ ñèìïòîì³â (ïåíòàäè): îæèð³ííÿ, ã³ïîãåí³òàë³çì, ðîçóìîâà â³äñòàë³ñòü, ïîë³äàêòèë³ÿ, ï³ãìåíòíèé ðåòèí³ò. Äåÿê³ àâòîðè íàâîäÿòü ïðèêëàäè ïàö³ºíò³â, ÿê³ îïèñàí³ â ë³òåðàòóð³ ç äîäàòêîâèìè "âèïàäêîâèìè" ðèñàìè, òàêèìè, ÿê äâàðô³çì (êàðëèêîâ³ñòü), àòðîô³ÿ çîðîâîãî íåðâà áåç ï³ãìåíòíîãî ðåòèí³òó, í³ñòàãì, ñòðàá³çì, ãëóõîòà, âðîäæåíà âàäà ñåðöÿ ³ äåôîðìàö³ÿ ÷åðåïà. Íåçâàæàþ÷è íà âàð³àáåëüí³ñòü ñèíäðîìó, áóëî ðåêîìåíäîâàíî íàçèâàòè éîãî ÿê "Ëîóðåíñà - Ìóíà - Á³äëÿ", öåé òåðì³í âêîðåíèâñÿ â ë³òåðàòóð³ ³ âèêîðèñòîâóºòüñÿ äëÿ ìåäèêî-ãåíåòè÷íîãî êîíñóëüòóâàííÿ. ñåñòðà ïàö³ºíòà, ÿêèé ïîìåð â³ä ïóõëèíè ìîçêó íåâèçíà÷åíîãî ïîõîäæåííÿ, ìàëà îçíàêè "ã³ïîô³çàðíîãî ³íôàíòèë³çìó ³ ïîë³äàêòè볿". Laurence-Moon Syndrome Bardet-Biedl Syndrome, Type 2; BBS2

29. DeCS - Changed Terms SYNDROME. LAURENCEMOON-BIEDL SYNDROME, laurence-moon syndrome. MAXIMUMPERMISSIBLE EXPOSURE LEVEL, MAXIMUM ALLOWABLE CONCENTRATION. http://decs.bvs.br/I/rep_i2000.htm

30. Laurence-Moon Syndrome Website Results :: Linkspider UK laurencemoon syndrome Websites from Linkspider UK. Keyword Laurence-MoonSyndrome. Linkspider UK Directory laurence-moon syndrome Search for. http://www.linkspider.co.uk/Health/ConditionsandDiseases/GeneticDisorders/Lauren

Laurence-Moon Syndrome Websites from Linkspider UK Keyword: Laurence-Moon Syndrome Linkspider UK Directory Laurence-Moon Syndrome Search for Directory Tree: Top Health Conditions and Diseases Genetic Disorders : Laurence-Moon Syndrome (4) Add URL Advertise Here! Personalize Amazon ... Weather See Also: Health: Conditions and Diseases: Neurological Disorders: Brain Diseases Health: Conditions and Diseases: Rare Disorders 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. NORD - Laurence Moon Syndrome - Offers alternative names, a general discussion and further resources. Pediatric Database - A definition of Laurence-Moon syndrome followed by the epidemiology, pathogenesis, clinical features, investigations and management. National Library of Medicine - A look at the former names of Laurence-Moon syndrome, a summary and a list of clinical features.

31. Alphabetical Topic Index (AZ) Jump To A B C D E F G H I J K L M Medullary Syndrome Lateral Sinus Thrombosis Lateral Sinus Thrombosis Latex AllergyLatex Allergy Lathyrism Lathyrism laurencemoon syndrome Laurence-Moon http://www.uscuh.com/apps/Intermap/topiclist/SectionL.html

Alphabetical Topic Index (A-Z): Jump To: A B C D ... Ly L La Labyrinthitis Labyrinthitis Lacerations Lacerations Lacrimal (Tear) Duct Obstruction Lacrimal Duct Obstruction Lactic Acidosis Lactic Acidosis Lactose Intolerance Lactose Intolerance Lafora Disease Lafora Disease Lambert-Eaton Myasthenic Syndrome Lambert-Eaton Myasthenic Syndrome Landau-Kleffner Syndrome Landau-Kleffner Syndrome Langer-Giedion Syndrome Langer-Giedion Syndrome Language Development Disorders Language Development Disorders Larva Migrans Larva Migrans Laryngeal Edema Laryngeal Edema Laryngismus Laryngismus Laryngostenosis Laryngostenosis Lassa Fever Lassa Fever Lateral Medullary Syndrome Lateral Medullary Syndrome Lateral Sinus Thrombosis Lateral Sinus Thrombosis Latex Allergy Latex Allergy Lathyrism Lathyrism Laurence-Moon Syndrome Laurence-Moon Syndrome Back To Top ^ Le Lead Poisoning Lead Poisoning Lead Poisoning, Nervous System, Adult Lecithin Acyltransferase Deficiency Lecithin Acyltransferase Deficiency Leg Dermatoses Leg Dermatoses Leg Length Inequality Leg Length Inequality Legg-Perthes Disease Legg-Perthes Disease Legionnaires' Disease Legionnaires' Disease Leigh Disease Leigh Disease Leiomyoma, Epithelioid

32. Medicalseek - Search Engine For The Healthcare Industry Conditions and DiseasesGenetic Disorderslaurencemoon syndrome Laurence MoonBardet Biedl Society Fully accessible site for people with LMBB, their families http://www.medicalseek.net/Conditions_and_Diseases_Genetic_Disorders_Laurence_Mo

CATEGORIES ADD A LINK ADVERTISE CONTACT US ... Genetic Disorders Laurence-Moon Syndrome Conditions and Diseases:Genetic Disorders:Laurence-Moon Syndrome 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. lmbbs.org.uk National Library of Medicine A look at the former names of Laurence-Moon syndrome, a summary and a list of clinical features. nlm.nih.gov/cgi/jablonski/syndrome_cgi?... NORD - Laurence Moon Syndrome Offers alternative names, a general discussion and further resources. stepstn.com/cgi-win/nord.exe?proc=GetDo... Pediatric Database A definition of Laurence-Moon syndrome followed by the epidemiology, pathogenesis, clinical features, investigations and management. icondata.com/health/pedbase/files/LAURE... CATEGORIES ADD A LINK ADVERTISE CONTACT US ... FORUMS

33. Laurence-moon Syndrome (codes) Name LAWRENCEMOON SYNDROME Synonyms, laurence-moon syndrome (codes). 1993Dec; 50(10) 859-62 Laurence-Moon-Biedl syndrome report of two cases. http://malattierare.pediatria.unipd.it/pubblicaMR/mr_dx_ing.asp?mr=203

34. LMB pigmentary changes. laurencemoon syndrome autosomal recessive disorder;mental retardation; spinal paraparesis; progressive retinal http://www.mrcophth.com/ww/LMB.html

Laurence, John Z (1829 - 1870) Moon, Robert C (1845 - 1914) Biedl, Arthur ( 1869 - 1933) Laurence-Moon-Biedl (Bield-Bardet) syndrome autosomal recessive disorder obesity mental retardation polydactly hypogonadism progressive retinal dystrophy and pigmentary changes Laurence-Moon syndrome autosomal recessive disorder mental retardation spinal paraparesis progressive retinal dystrophy and pigmentary changes NO obesity or polydactly Curriculum Vitae (Laurence, John Zachariah) Nationality: English ophthalmologist Undergraduate: University College, London Qualified 1854 Postgraduate: Founder of South London Ophthalmic Hospital (later known as Royal Eye Hospital) Ophthalmic surgeon, St. Bartholomew's Hospital, Rochester Publication: LaurenceJZ, Moon RC (1866) Four cases of retinitis pigmentosa occurring in the same family and accompanied by general imperfection of development. Ophthalmol Rev 2:32 Curriculum Vitae (Moon, Robert Charles) Nationality: English ophthalmologist in Philadelphia, USA Born in Brighton, England Undergraduate: Medical degree in London Postgraduate: Surgeon, South London Ophthalmic Hospital 1866 - 1878

35. Laurence-Moon-Bardet-Biedl Syndrome Network Home Page Raises public awareness of the laurencemoon Bardet-Biedl syndrome and serves as a place for parents of LMBBS children to meet and exchange ideas. http://www.geocities.com/HotSprings/Spa/1761/

Welcome to the Laurence-Moon-Bardet-Biedl Network Home Page The purpose of this page is to raise public awareness of the Laurence-Moon Bardet-Biedl syndrome. It will also serve as a place for parents of LMBBS children to meet and exchange ideas. Next Page You are visitor # Since 23 Sept 97 This Blindness and Visual Impairment site owned by Mary Morris Previous 5 Sites Skip Previous Previous ... List Sites This page hosted by

36. LMBBS Home Page The cardinal manifestations of BardetBiedl syndrome, a form of laurence-moon-Biedlsyndrome. The spectrum of renal disease in laurence-moon-Biedl syndrome. http://www.isgrd.umds.ac.uk/laurence/laurence5.htm

WHERE TO GET HELP The LMBBS Society Spring Grove Loudhams Wood Lane Chalfont St Giles Bucks HP8 4AR Tel: 01494 764924 British Retinitis Pigmentosa Society PO Box 350 Buckingham MK18 5EL Tel: +44 1280 860363 Fax: +44 1280 860515 Royal National Institute for the Blind 224 Great Portland Street London W1N 6AA Tel: +44 171 388 1266 Fax: +44 171 388 2034 Genetic Interest Group (GIG) Farringdon Point 29-35 Farringdon Road London EC1M 3JB Tel: +44 171 430 0090 Fax: +44 171 430 0092 Contact A Family 170 Tottenham Court Road London W1P 0HA Tel: +44 171 383 3555 Fax: +44 171 383 0259 Obesity Research Centres: Dr. Peter Kopelman MD FRCP Obesity Research Centre Medical Unit 5th Floor Alexandra Wing Royal London Hospital Whitechapel London E1 1BB Tel: +44 171 377 7696 Fax: +44 171 377 7636 Ms. Clare Grace M.Sc. (Dietician) Obesity Research Centre Medical Unit 5th Floor Alexandra Wing Royal London Hospital Whitechapel London E1 1BB Tel: +44 171 377 7420 Fax: +44 171 377 7636 Dr. Nick Finer MD FRCP

37. The Contact A Family Directory - BARDET-BIEDL SYNDROME Information about laurencemoon-bardet-biedl syndrome, its symptoms and inheritance patterns. http://www.cafamily.org.uk/Direct/b10.html

printer friendly BARDET-BIEDL SYNDROME home more about us in your area conditions information ... how you can help search this site Bardet-Biedl Syndrome (BBS): Laurence-Moon-Bardet-Biedl Syndrome The syndrome is a rare inherited condition which is variable in the way in which it presents. Characteristics are rod/cone dystrophy (atypical retinitis pigmentosa - a progressive eye condition which can lead to blindness (see Visual Impairment )); obesity (usually with an early onset and resistant to treatment); polydactyly (extra fingers and/or toes); hypogenitalism (underdeveloped genitals); mild to severe learning difficulties. Usually four out of these five features are required to make the diagnosis. In addition, there are other important characteristics which need to be taken into account: kidney malformations and renal dysfunction; developmental delay; speech difficulties; diabetes mellitus and, rarely, diabetes insipidus; hepatic fibrosis and other hormonal deficiencies. In the Middle-East and island communities such as Newfoundland, the condition is relatively common, occurring at rates of 1 in 13,500 of the population. In Europe and the UK the prevalence is much less common owing to lower consanguinity. The figure is probably around 1 in 100,000 of the population. Although BBS is not common it is certainly under diagnosed. As awareness of the condition increases, the number of people identified is growing every year.

38. Clinical Information laurencemoon-Bardet-Biedl syndrome. There is currently a support networkfor those affected by laurence-moon-Bardet-Biedl syndrome. http://www.geocities.com/HotSprings/Spa/1761/clinical.html

Laurence-Moon-Bardet-Biedl Syndrome Bardet-Biedl syndrome is a complex disorder that involves many parts of the body. Individuals with the disorder have retinal degeneration similar to that caused by retinitis pigmentosa and may have many other characteristic symptoms. The abstracts that are listed are for the parent or individual to become more familiar with the many aspects of Laurence-Moon-Bardet-Biedl syndrome. If you have questions concerning the information you find please print the abstract and take it with you to your doctor! The information he/she needs to obtain a complete article is on the print out. Bardet-Biedl type 1 Bardet-Biedl type 2 Bardet-Biedl type 3 Bardet-Biedl type 4 ... Additional Links There is currently a support network for those affected by Laurence-Moon-Bardet-Biedl syndrome. Please contact: Mary Morris 100 Van Buren Ave. Biloxi, MS 39531 Email REMEMBER TO SIGN OUR GUEST BOOK! Sign Guestbook View Guestbook BACK Geocities

39. Macular Degeneration, Retinitis Pigmentosa, Stargardt Disease, Usher Syndrome, R Juvenile Macular Degeneration, Retinoschisis. laurencemoon Bardet-Biedel syndrome,Leber Congenital Amaurosis. laurence-moon Bardet-Biedl syndrome, Lutein. http://www.blindness.org/appendix.asp

Macular Degeneration Retinitis Pigmentosa Usher Syndrome Stargardt Disease ... Register Macular Degeneration, AMD, Retinitis Pigmentosa, Stargardt Disease, Usher Syndrome, Bardet-Biedl Syndrome, Eye Diseases, Tunnel Vision, Retinal Degenerative Diseases, Vision Problems The Foundation Fighting Blindness is a publicly-supported charity raising money to fund research for macular degeneration, retinitis pigmentosa (RP), Usher syndrome and related diseases. We provide information, resources and referrals. Find more information about the following terms: Age Related Macular Degeneration AMD Amsler Amsler Grid ... Back to Top

40. Laurence-moon, Syndrome : Arborescences MeSH Translate this page laurence-moon, syndrome. hypophyse, maladies C10.228.140.617.738 + page CISMeF dumotclef laurence-moon, syndrome C10.228.140.617.500 page CISMeF du motclef http://www.chu-rouen.fr/navimesh/navilaurencemoonsyndrome.html

Laurence-moon, Syndrome : arborescences MeSH Menu général CISMeF Vous pouvez aussi consulter toutes les arborescences des mots clés utilisés dans CISMeF système nerveux, maladies système nerveux central, maladies encéphalopathies hypothalamus, maladies ... Zellweger, syndrome 27 février 2003 courriel Menu général CISMeF Haut de page © CHU de Rouen . Toute utilisation partielle ou totale de ce document doit mentionner la source.

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