1. LMBBS Home Page laurencemoon syndrome (LMS) is characterised by retinitis pigmentosa (more accurately termed rod-cone dystrophy), mental retardation, hypogenitalism and http://www.isgrd.umds.ac.uk/laurence/

Division of Molecular and Medical Genetics Prince Philip Research Laboratories Guy's Hospital London Laurence-Moon-Bardet-Biedl Syndrome (LMBBS) This page is aimed primarily at medical and health-care professionals involved in the care of LMBBS patients and also for parents or relatives wishing to know more about the syndrome and the implications for those affected. CONTENTS History Eye signs Obesity Learning difficulties ... Genetic Advice Treatment Rod-Cone dystrophy Polydactyly Obesity Learning difficulties ... References and useful publications HISTORY rod-cone dystrophy ), mental retardation, hypogenitalism and spastic paraparesis. Bardet-Biedl syndrome (BBS) has as the main features RP (rod-cone dystrophy), obesity, postaxial polydactyly, learning disabilities and hypogenitalism (males). This latter subgroup represents by far the majority of published cases and is now the preferred term amongst the medical and scientific community. As there are many cases of overlap between the LMS and BBS we shall for the purposes of this publication make no distinction and therefore refer to LMBBS throughout. John Zachariah Laurence c.1870

2. NORD - National Organization For Rare Disorders, Inc. General Discussion. laurencemoon syndrome is a rare inherited disorder characterized by literature regarding the difference between laurence-moon syndrome and Bardet-Biedl Syndrome http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Laurence Moon

3. Laurence-Moon Syndrome Information Diseases Database laurencemoon syndrome, Disease Database Information Sponsors Contact Previous Page. laurence-moon syndrome Information. laurence-moon syndrome Definition(s) via UMLS ..Code translations and terms via UMLS http://www.diseasesdatabase.com/ddb30072.htm

Diseases Database Index Sponsors Contact ... Previous Page Laurence-Moon syndrome Information Search Laurence-Moon syndrome may cause or feature (Follow link for list) belong(s) to the category of (Follow link for list) Laurence-Moon syndrome: Definition(s) via UMLS Code translations and terms via UMLS Laurence-Moon syndrome: specific sites Send Laurence-Moon syndrome to medical search engines (JavaScript enabled browsers only) If your browser has no JavaScript you can still use these: Search using Internet medical databases Search using Internet search engines (non-specialist) We subscribe to the HONcode principles of the Health On the Net Foundation i-medicine.info - the evidence based medicine, informatics and audit portal Valid XHTML 1.0 Served 2004-06-02 23:36:53 Metadata Updated 2004-05-22

4. Laurence Moon Bardet Biedl Syndrome Lauurence Moon Bardet Biedl Syndrome Resources, international support groups, clinics, genetic counselors and geneticists Hospital London. laurencemoon syndrome, Pediatric Database (PEDBASE) Laurence-Moon http://www.kumc.edu/gec/support/laurmoon.html

Laurence Moon Bardet Biedl Syndrome Laurence Moon Bardet Biedl Syndrome Network Laurence-Moon-Bardet-Biedl Syndrome , Canada Laurence-Moon-Bardet-Biedl Syndrome (LMBBS) , Molecular and Medical Genetics, Prince Philip Research Laboratories, Guy's Hospital London Laurence-Moon Syndrome , Pediatric Database (PEDBASE) Laurence-Moon-Bardet-Biedl (LMBB) , Senter for sjeldne sykdommer og syndromer Smågruppesenteret på Rikshospitalet Centre for Rare Disorders Laurence-Moon-Bardet-Biedl Society , United Kingdom Bardet-Biedl Laurence-Moon Syndrome , Belgium or Dutch LMBBS discussion group,(Laurence Moon Baardet-Beidl Syndrome) , Australia Syndrome de Laurence-Moon-Bardet-Biedl France Laurence-Moon Syndrome , Online Mendelian Inheritance in Man (OMIM) #245800 Bardet-Biedl Syndrome (BBS) , Online Mendelian Inheritance in Man (OMIM) Laurence Moon , signs of condition, Orphanet Laurence-Moon-Bardet-Biedl Syndrome , WideSmiles Also See: National organizations information on genetic conditions or birth defects Information for siblings and family members , genetic conditions Vision Impairment / Blindness Resources To locate a genetic counselor or clinical geneticist in your area: Professional Genetics Societies Genetic clinics, centers, departments

5. Laurence-Moon Syndrome Multiple Congenital Anomaly/Mental Retardation (MCA/MR) Syndromes. View the Full Record. Syndrome. laurencemoon syndrome. Summary. A syndrome of mental retardation, retinitis pigmentosa, hypogonadism, and spastic paraplegia. and spastic paraplegia. Laurence-Moon-Biedl syndrome and Laurence-Moon-Biedl-Bardet syndrome are no http://www.nlm.nih.gov/mesh/jablonski/syndromes/syndrome393.html

Multiple Congenital Anomaly/Mental Retardation (MCA/MR) Syndromes View the Full Record Syndrome Laurence-Moon syndrome Summary A syndrome of mental retardation, retinitis pigmentosa, hypogonadism, and spastic paraplegia. Laurence-Moon-Biedl syndrome and Laurence-Moon-Biedl-Bardet syndrome are no longer considered as valid terms in that patients with Laurence and Moon had spastic paraplegia but no polydactyly and obesity which were the key elements in the Bardet and Biedl patients. Bardet-Biedl syndrome is a separate entity. Major Features Eyes: Pigmentary retinopathy. Nervous system: Spastic paraplegia. Urogenital system: Hypogonadism. Growth and development: Mental retardation. Heredity: The syndrome is familial and is transmitted as an autosomal recessive trait. View the Full Record U.S. National Library of Medicine , 8600 Rockville Pike, Bethesda, MD 20894 National Institutes of Health Privacy Accessibility Last updated: 27 October 1999

6. National Library Of Medicine Laurence-Moon Syndrome A look at its former names, a summary and a list of clinical features. http://www.nlm.nih.gov/cgi/jablonski/syndrome_cgi?term=Laurence-Moon syndrome&am

7. NORD - National Organization For Rare Disorders, Inc. Confusion exists in the medical literature regarding the difference between BardetBiedl Syndrome and laurence-moon syndrome. . http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Bardet Biedl

8. Pediatric Database A definition of laurencemoon syndrome followed by the epidemiology, pathogenesis, clinical features, investigations and management. http://www.icondata.com/health/pedbase/files/LAURENCE.HTM

9. Laurence-Moon Syndrome - Information / Diagnosis / Treatment / Prevention home genetic disorders laurencemoon syndrome laurence-moon syndrome. Information • Diagnosis • Treatment • Prevention. http://www.healthcyclopedia.com/genetic-disorders/laurence-moon-syndrome.html

Home Health cyclopedia All Topics by Category The Good Health Search Engine Health Conditions A-Z Gurus ... genetic disorders > laurence-moon syndrome Laurence-Moon Syndrome Information / Diagnosis / Treatment / Prevention External links (marked with an arrow ) open in a new window. This site is a web directory and does not offer medical advice. We cannot take responsibility for information found on listed sites. This Page Related Topics Medical Definition Health News Web Directory: Related Topics: Neurological Disorders/Brain Diseases Rare Disorders Medical Definition: University of Newcastle-upon-Tyne Medical Dictionary: "laurence-moon-biedl syndrome" Health News: Search millions of published articles for news on Laurence-Moon Syndrome Modern Medicine Aging The Ardell Wellness Report HealthFacts Medical Post Medical Update Men's Health and the National Women's Health Report Note: Subscription required to access the full text of articles. Web Directory: 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. National Library of Medicine: Laurence-Moon Syndrome A look at its former names, a summary and a list of clinical features.

10. Laurence Moon Syndrome Laurence Moon Syndrome. Confusion exists in the medical literature regarding the difference between laurencemoon syndrome and Bardet-Biedl Syndrome. http://www.bchealthguide.org/kbase/nord/nord104.htm

document.write(''); var hwPrint=1; var hwDocHWID="nord104"; var hwDocTitle="Laurence Moon Syndrome"; var hwRank="1"; var hwSectionHWID="nord104"; var hwSectionTitle=""; var hwSource="cn6.0"; var hwProdCfgSerNo="wsh_html_031_s"; var hwDocType="NORD"; National Organization for Rare Disorders, Inc. Laurence Moon Syndrome Important It is possible that the main title of the report is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. Synonyms Adipogenital-Retinitis Pigmentosa Syndrome Laurence Syndrome LM Syndrome Disorder Subdivisions None Related Disorders List Information on the following diseases can be found in the Related Disorders section of this report: Bardet-Biedl Syndrome Prader-Willi Syndrome Borjeson Syndrome Hypogonadotrophic Hypogonadism Alstrom Syndrome Weiss Syndrome Biemond II General Discussion Laurence-Moon Syndrome is a rare inherited disorder characterized by diminished hormone production by the testes or ovaries (hypogonadism), progressive loss of vision (retinitis pigmentosa), mental retardation, and paralysis of the legs and lower part of the body accompanied by involuntary muscle contractions (spastic paraplegia). Confusion exists in the medical literature regarding the difference between Laurence-Moon Syndrome and Bardet-Biedl Syndrome. Some researchers believe that Bardet-Biedl Syndrome is a subdivision of Laurence-Moon Syndrome which they term "Laurence-Moon-Biedl Syndrome."

11. Bardet Biedl Syndrome Confusion exists in the medical literature regarding the difference between BardetBiedl Syndrome and laurence-moon syndrome. . Symptoms. http://www.bchealthguide.org/kbase/nord/nord988.htm

document.write(''); var hwPrint=1; var hwDocHWID="nord988"; var hwDocTitle="Bardet Biedl Syndrome"; var hwRank="1"; var hwSectionHWID="nord988"; var hwSectionTitle=""; var hwSource="cn6.0"; var hwProdCfgSerNo="wsh_html_031_s"; var hwDocType="NORD"; National Organization for Rare Disorders, Inc. Bardet Biedl Syndrome Important It is possible that the main title of the report is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. Synonyms Biedl-Bardet Syndrome Disorder Subdivisions None Related Disorders List Information on the following diseases can be found in the Related Disorders section of this report: Alstrom Syndrome Laurence-Moon Syndrome McKusick-Kaufman Syndrome Prader-Willi Syndrome General Discussion Bardet-Biedl Syndrome is a group of rare disorders inherited as autosomal recessive genetic traits. Major features of these disorders may include mental retardation, obesity, delayed sexual development or underdeveloped reproductive organs, progressive pigmentary degeneration of the retinas of the eyes, kidney abnormalities in structure or function, and/or abnormal or extra fingers and/or toes. Confusion exists in the medical literature regarding the difference between Bardet-Biedl Syndrome and Laurence-Moon Syndrome. Symptoms The Bardet-Biedl Syndromes are also frequently characterized by abnormalities of the numbers of fingers and/or toes (digits) as well as obesity that is often limited to the trunk. Digital abnormalities may include extra fingers and/or toes (polydactyly), webbing of certain digits (syndactyly) (characteristically the second and third toes), and/or abnormal shortness of the digits (brachydactyly) compared to the palm length. In addition, the feet tend to be unusually short, broad, and flat, with no arch.

12. WebMD Health - 404 Error More results from my.webmd.com OMIM laurence-moon syndrome http://my.webmd.com/content/healthwise/82/20340

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13. Bardet-Biedl Syndrome (BBS) markers on chromosome 16. LaurenceMoon-Biedl syndrome and Laurence-Moon-Biedl-Bardet syndrome are no the Bardet-Biedl the syndrome. laurence-moon syndrome is a separate entity http://www.nlm.nih.gov/mesh/jablonski/syndromes/syndrome048.html

Multiple Congenital Anomaly/Mental Retardation (MCA/MR) Syndromes View the Full Record Syndrome Bardet-Biedl syndrome (BBS) Summary A syndrome characterized mainly by obesity, pigmentary retinopathy, polydactyly, mental retardation, hypogonadism, and renal failure in fatal cases. Two forms have been identified: Bardet-Biedl syndrome 1 (BBS1) has no linkage to chromosome 16 Bardet-Biedl syndrome 2 (BBS2) is mapped to markers on chromosome 16. Laurence-Moon-Biedl syndrome and Laurence-Moon-Biedl-Bardet syndrome are no longer considered as valid terms in that patients of Laurence and Moon had paraplegia but no polydactyly and obesity which are the key elements of the Bardet-Biedl the syndrome. Laurence-Moon syndrome is a separate entity. Major Features Eyes: Pigmentary retinopathy. Hand and foot: Polydactyly. Cardiovascular system: Hypertrophy of interventricular septum and left ventricle and dilated cardiomyopathy. Gastrointestinal system: Fibrosis. Urogenital system: Hypogonadism, renal failure, urogenital sinuses, ectopic urethra, uterus duplex, septate vagina, and hypoplasia of the uterus, ovaries, and fallopian tubes. Growth and development: Mental and growth retardation.

14. OMIM - %245800 LAURENCE-MOON SYNDROME %245800 laurencemoon syndrome. TEXT. The laurence-moon syndrome (strictu sensu) is the same as the disorder reported by Kapuscinski (1934). http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?cmd=entry&id=245800

15. Disease Directory : Genetic Disorders : Laurence-Moon Syndrome Diseases Genetic Disorders laurencemoon syndrome. Some; Conditions and Diseases Genetic Disorders laurence-moon syndrome http://www.diseasedirectory.net/Genetic_Disorders/Laurence-Moon_Syndrome/default

Wednesday, June 02, 2004 Genetic Disorders Aarskog Syndrome Aase Syndrome Ablepharon-Macrostomia Syndrome ... Genetic Disorders : Laurence-Moon Syndrome Bardet-Biedl Syndrome, Laurence-Moon/Bardet-Biedl,Biedl-Bardet ... - Confusion exists in the medical literature regarding the difference between Bardet-Biedl Syndrome and Laurence-Moon Syndrome. Some Conditions and Diseases: Genetic Disorders: Laurence-Moon Syndrome ... - Conditions and Diseases: Genetic Disorders: Laurence-Moon Syndrome. See also: Health: Conditions and Diseases: Neurological Disorders: Brain Diseases (117); Genetic Disorders / Laurence-Moon Syndrome - Genetic Disorders / Laurence-Moon Syndrome. Categories related to Laurence-Moon Syndrome: Geometry.Net - Health_Conditions: Laurence-moon Syndrome - Pediatric Database (PEDBASE). Discipline: GEN; Last Updated: 12/23/94 LAURENCE-MOON SYNDROME. DEFINITION: Laurence-Moon syndrome. Direct access to details Alias : Health Information Resource Database: Laurence-Moon-Biedl Syndrome ... - Laurence-Moon-Biedl Syndrome Network. Contact Information. Sonya Coster 124 Lincoln Ave Purchase, NY 10577. 914-251-1163 (Voice). Internet Resources. Health Library - Laurence Moon Syndrome - Laurence Moon Syndrome. Confusion exists in the medical literature regarding the difference between Laurence-Moon Syndrome and Bardet-Biedl Syndrome.

16. Disease Directory : OMIM - *245800 LAURENCE-MOON SYNDROME Diseases Genetic Disorders laurencemoon syndrome OMIM - *245800 laurence-moon syndrome. Directory Listing. Title OMIM - *245800 http://www.diseasedirectory.net/detailed/25769.aspx

Wednesday, June 02, 2004 Genetic Disorders Aarskog Syndrome Aase Syndrome Ablepharon-Macrostomia Syndrome ... Laurence-Moon Syndrome : OMIM - *245800 LAURENCE-MOON SYNDROME Directory Listing Title: OMIM - *245800 LAURENCE-MOON SYNDROME Description: *245800 LAURENCE-MOON SYNDROME. TEXT. The Laurence-Moon syndrome (strictu sensu) is the same as the disorder reported by Kapuscinski (1934). Date Added: 2/16/2004 7:19:18 PM URL:

17. Conditions And Diseases - Laurence-Moon Syndrome Top Links laurencemoon syndrome Web Site Links. NORD - Laurence Moon Syndrome - Offers alternative names, a general discussion and further resources. http://www.disease-resources.com/Top_Health_Conditions_and_Diseases_Genetic_Diso

Sub Categories Related Healthcare Subjects Disabilities Environmental Health Fitness Health Insurance ... Men's Health Laurence-Moon Syndrome Web Site Links 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. Other Useful Health Web Links National Institutes of Health (NIH) US Government department in charge of medical research. AHRQ: Clinical Information Clinical information on evidence-based practice, clinical guidelines, medical effectiveness, pharmaceutical therapy, new technology, screening and preventive services, outcomes research, and the National Guideline Clearinghouse. The UK Health Technology Assessment Programme Site contains details of program's many projects and publications; an NHS national research and development initiative.

18. Genetic Disorders, Laurence-Moon Syndrome Submit Your Site to the laurencemoon syndrome category. Sponsored laurence-moon syndrome Sites. Submit Your Site to the laurence-moon syndrome category. http://www.iseekhealth.com/laurence-moon_syndrome-1595.php

Home About Us Contact Submit Your Site Search : Home Health Conditions and Diseases Genetic Disorders ... Laurence-Moon Syndrome More Laurence-Moon Syndrome Categories: Submit Your Site to the Laurence-Moon Syndrome category Sponsored Laurence-Moon Syndrome Sites Cystic Fibrosis Book Store At WellnessBooks.com Comprehensive source to books on Cystic Fibrosis. Includes community boards and chat, book reviews and online ordering. Buy Genetic Disorders Products We link to merchants which offer Genetic Disorders products for sale. Online Doctors - Ask Us Now! Kasamba's variety of health experts- including Doctors, Specialists, Herbalists, Nurses and more- offer real help for affordable consultation fees- live via chat or e-mail! Buy Genetics Books At Amazon.com and Save! Would you like to save on Genetics Books at Amazon and other stores? Compare prices at BookSellersNow.com! Our site continually proves that online shopping can be fun! 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. National Library of Medicine: Laurence-Moon Syndrome - A look at its former names, a summary and a list of clinical features.

19. Genetic Disorders, Laurence-Moon Syndrome Category Home Health Conditions and Diseases Genetic Disorders laurencemoon syndrome. * Site Title · The name of the site. http://www.iseekhealth.com/directory/index.php?method=show_link_exchange&directo

20. Laurence-Moon Syndrome,Adipogenital-Retinitis Pigmentosa Syndrome,Laurence Syndr Laurence Moon Syndrome Confusion exists in the medical literature regarding the difference between laurencemoon syndrome and Bardet-Biedl Syndrome. http://www.icomm.ca/geneinfo/laurmoon.htm

Laurence-Moon Syndrome,Adipogenital-Retinitis Pigmentosa Syndrome,Laurence Syndrome,LM Syndrome For Information on Workshops and Seminars for Special Needs Children click here The GAPS INDEX to Information on the Internet about Genetic Disorders and Birth Defects Genetic Information and Patient Services, Inc. (GAPS) HOME DISORDERS GLOSSARY Laurence Moon Syndrome also known as: Adipogenital-Retinitis Pigmentosa Syndrome Laurence Syndrome LM Syndrome (as defined by the National Organization for Rare Disorders Laurence-Moon Syndrome is a rare inherited disorder characterized by diminished hormone production by the testes or ovaries (hypogonadism), progressive loss of vision (retinitis pigmentosa), mental retardation, and paralysis of the legs and lower part of the body accompanied by involuntary muscle contractions (spastic paraplegia). Confusion exists in the medical literature regarding the difference between Laurence-Moon Syndrome and Bardet-Biedl Syndrome. Some researchers believe that Bardet-Biedl Syndrome is a subdivision of Laurence-Moon Syndrome which they term "Laurence-Moon-Biedl Syndrome." Find more information on the Internet with Select name of the disorder Laurence-Moon Syndrome Adipogenital-Retinitis Pigmentosa Syndrome Laurence Syndrome LM Syndrome SUPPORT GROUPS and information sites: American Foundation for the Blind 11 Penn Plaza New York NY 10001 USA e-mail: afbinfo@afb.org

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