1. 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

2. Laurence-Moon Syndrome Syndrome laurencemoon syndrome. Summary. A syndrome of mental retardation, retinitis pigmentosa, hypogonadism, and spastic paraplegia. http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

3. Laurence-Moon-Bardet-Biedl Syndrome / Family Village Library LaurenceMoon-Bardet-Biedl Syndrome http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

4. UMDS LMBBS Information for healthcare professionals involved in the care of Laurence-Moon-Bardet-Biedl Syndrome patients and for parents or relatives seeking http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

5. Laurence Moon Syndrome laurencemoon syndrome is a rare inherited disorder characterized by diminishedhormone production by the testes or ovaries (hypogonadism), progressive loss http://www.bchealthguide.org/kbase/nord/nord104.htm

var hwPrint=1;var hwDocHWID="nord104";var hwDocTitle="Laurence Moon Syndrome";var hwRank="1";var hwSectionHWID="nord104-Header";var hwSource="en-caQ2_05";var hwDocType="Nord"; National Organization for Rare Disorders, Inc. Laurence Moon Syndrome Important It is possible that the main title of the report Laurence Moon Syndrome 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 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." Resources National Association for Visually Handicapped 22 West 21st Street New York, NY 10010

6. Laurence-Moon-Bardet-Biedl Syndrome Network 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://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

7. Laurence-Moon Syndrome Information Diseases Database laurencemoon syndrome, Disease Database Information. 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 web 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 Valid XHTML 1.0 Served 2005-09-09 10:04:54 View metadata Last major update 2005-09-03. The medical information here is presented for education, background reading and general interest. The Diseases Database is not a diagnostic or clinical decision-making tool. Please consult your own licensed physician regarding diagnosis and treatment of any medical condition! Content is not asserted complete or error free, please see also our

8. Laurence Moon Bardet Biedl Society LaurenceMoon-Bardet-Biedl Society http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

9. Laurence-Moon Syndrome Syndrome, laurencemoon syndrome. Summary, A syndrome of mental retardation, 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

10. Laurence Moon Syndrome laurencemoon syndrome is a rare inherited disorder characterized by diminished hormone production by the testes or ovaries (hypogonadism) http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

11. Search Jablonski's Syndromes Database 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&fi

12. LAURENCE-MOON SYNDROME laurencemoon syndrome http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

13. D Bats Listesnof Syndrome De Laurence-Moon-Bardet-Biedl D bats listesnof sommaire Syndrome de LaurenceMoon-Bardet-Biedl 09/07/98 Chers Amis http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

14. Short Description Of Cell Lines. Pathology: Laurence-Moon Syndrome *245800 Pathology laurencemoon syndrome *245800 OMIM record. - By selecting the cellline name, you will receive the detailed description of the cell line http://www.biotech.ist.unige.it/cldb/pat106.html

Version Short description of cell lines. Pathology: Laurence-Moon syndrome OMIM record By selecting the cell line name , you will receive the detailed description of the cell line By selecting one of the terms between parentheses, you will receive the list of all relevant cell lines You can search any term of the list by using the 'Find' utility of your browser human, Caucasian skin, fibroblast GEIMM human, Caucasian ... By Beatrice...

15. Laurence Moon/Bardet Biedl Syndrome Laurence Moon/ Bardet Biedl Syndrome LMBBS Home page This page is aimed primarily at medical and healthcare professionals involved in the care http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

16. Bardet-Biedl Syndrome, Laurence-Moon/Bardet-Biedl Biedl-Bardet BardetBiedl Syndrome Laurence-Moon/Bardet-Biedl Bie http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

17. Laurence-Moon Syndrome Topic - Unified Search Environment This syndrome was previously referred to as LaurenceMoon-Biedl syndrome untilBARDET-BIEDL SYNDROME was identified as a distinct entity. http://www.use.hcn.com.au/portals/shared/subject.`Laurence-Moon Syndrome`/home.h

Laurence-Moon Syndrome Topic Tree Definition: 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) Synonyms and Source Vocabularies: Laurence-Moon Syndrome LAURENCE-MOON-BIEDL SYNDROME Lawrence Moon Biedl Syndrome Congenital Abnormality Abnormalities, Drug-Induced Abnormalities, Multiple Basal Cell Nevus Syndrome Beckwith-Wiedemann Syndrome Bloom Syndrome Cockayne Syndrome ... Congenital neurologic anomalies

18. Bardet-Biedl Syndrome (BBS) - Patient UK Differential Diagnosis laurencemoon syndrome (where affected individuals havea spastic paraparesis but no polydactyly), Cohen syndrome (CS). http://www.patient.co.uk/showdoc/40001347/

PatientPlus articles are written for doctors and so the language can be technical. However, some people find that they add depth to the articles found in the other sections of this website which are written for non-medical people. Bardet-Biedl Syndrome (BBS) This genetically heterogeneous disorder has a wide spectrum of clinical features. It follows a recessive pattern of inheritance with a modifier of penetrance (6 loci on 6 different chromosomes) A high incidence is found in Newfoundland (1:17,500 versus 1:160,000 elsewhere), Bedouins (1:13,500) and the Arab population of Kuwait. Male:Female ~ 1·3:1. The principal manifestations are rod-cone dystrophy (sometimes called atypical retinitis pigmentosa polydactyly syndactyly or brachydactyly (69%); central obesity mental retardation ; and hypogonadism Renal abnormalities are seen in almost all patients (characteristically fetal lobulation and calyceal cysts /diverticula/clubbing) which may cause renal impairment and failure. Other features which may be present include hepatic fibrosis, diabetes mellitus , reproductive abnormalities, endocrine disturbances, short stature myopia strabismus , and cataracts Differential Diagnosis Laurence-Moon syndrome (where affected individuals have a spastic paraparesis but no polydactyly), Cohen syndrome (CS).

19. Laurence-Moon Syndrome : Genetic Disorders : Disorders And Diseases : Health And Web Directory Health and Fitness Disorders and Diseases Genetic Disorders laurencemoon syndrome. laurence-moon syndrome (Subscribe) http://www.internet-web-directory.com/Health_and_Fitness/Disorders_and_Diseases/

Skip to Content Login/Register Web Directory by Internet-Web-Directory.com Web Directory Home ... Link Notify Search the entire directory only this category Advanced Search Web Directory Health and Fitness Disorders and Diseases ... Genetic Disorders Laurence-Moon Syndrome Laurence-Moon Syndrome Subscribe Links Laurence Moon Bardet Biedl Society http://www.lmbbs.org.uk Fully accessible site for people with LMBB, their families, friends, carers and interested professionals. Opinions, news, views, research, updates, and contact details. More Details Review It Rate It Bookmark It Sponsor Links Love Romance Dating Gift Ideas at Gifts-Shop.com Internet-Web-Directory.com

20. ScienceDaily -- Browse Topics: Health/Conditions_and_Diseases/Genetic_Disorders/ National Library of Medicine laurencemoon syndrome - A look at its former names, NORD Laurence Moon Syndrome - Offers alternative names, http://www.sciencedaily.com/directory/Health/Conditions_and_Diseases/Genetic_Dis

@import "/styles/navbar.css"; @import "/styles/tabStyles.css"; Set home page Bookmark site Add search Latest News ... Email to friend Text Size A A A Front Page ... Genetic Disorders : Laurence-Moon Syndrome Subtopics See Also: Health: Conditions and Diseases: Neurological Disorders: Brain Diseases Health: Conditions and Diseases: Rare Disorders Search Google: Laurence-Moon Syndrome News Books Links ... Tiny Enceladus May Hold Ingredients Of Life (September 8, 2005) full story Mayo Clinic Develops New Coma Measurement System (September 8, 2005) full story Nitric Oxide Could Extend Fertility (September 8, 2005) Biochemistry , an American Chemical Society journal. full story Cassini Reveals New Details About Saturn's Rings (September 6, 2005) full story New Observations Show Dynamic Particle Clumps In Saturn's A Ring (September 6, 2005) full story National Science Foundation Awards .2 Million To Large Synoptic Survey Telescope (September 6, 2005) full story Flipped, Expelled, Copied, And Shrunk: Researchers Document Dramatic Genome Alterations During Primate Evolution (September 6, 2005) Genome Research presents a series of studies that provide insight into the evolution and variation of primate genomes. The issue will appear online and in print on September 1, concomitant with the publication of the chimpanzee genome sequence in the journal

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