41. Laurence-Moon Syndrome laurencemoon syndrome Directory Guide to laurence-moon syndrome sites on the internet. laurence-moon syndrome. http://www.directory.net/Health/Conditions_and_Diseases/Genetic_Disorders/Lauren

Laurence-Moon Syndrome Directory: Guide to Laurence-Moon Syndrome sites on the internet. Search Engines: Google Yahoo MSN FindWhat ... City Guides Laurence-Moon Syndrome Health Conditions and Diseases Genetic Disorders Laurence-Moon Syndrome Websites 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. Pediatric Database http://www.icondata.com/health/pedbase/files/laurence.htm A definition of Laurence-Moon syndrome followed by the epidemiology, pathogenesis, clinical features, investigations and management. National Library of Medicine: Laurence-Moon Syndrome A look at its former names, a summary and a list of clinical features. NORD: Laurence Moon Syndrome http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=laurence%20moon%20syndrome Offers alternative names, a general discussion and further resources. Got eight minutes? Join in and participate in Stanford's Web Credibility Project's latest study.

42. Laurence-Moon Syndrome From Linkspider UK Health Directory Directory Topic laurencemoon syndrome assoicated to Health. Directory Tree Top Health Conditions and Diseases Genetic Disorders laurence-moon syndrome (). http://linkspider.co.uk/Health/ConditionsandDiseases/GeneticDisorders/Laurence-M

Match » -All words -Any word -Exact text Search » The Web Jobs / Vacancy Images / Photos FTP / Downloads United Kingdom United States of America Argentina Austria Australia Bangladesh Belgium Bolivia Brazil Bulgaria Canada Chile China Cuba Cyprus Czech Republic Czechoslovakia Denmark Dominican Republic Ecuador Egypt Estonia Finland France Germany Ghana Greece Hong Kong Hungary Iceland India Indonesia Ireland Israel Italy Japan Jordan Kenya Kuwait Latvia Lithuania Luxembourg Malaysia Malta Mexico Moldavia Monaco Morocco Mozambique Nepal Netherlands New Zealand Nicaragua Nigeria North Korea Norway Pakistan Panama Paraguay Peru Philippines Poland Portugal Qatar Romania Russian Federation Saudi Arabia Singapore South Africa South Korea Spain Sri Lanka Sweden Switzerland Taiwan Tanzania Thailand Tunisia Turkey Ukraine United Arab Emirates Uruguay Venezuela Yemen Yugoslavia Zambia Zimbabwe Ranking » On (no duplicate) Off (allow duplicate) Add my Site Toolbar Affiliates Directory Topic Laurence-Moon Syndrome assoicated to Health Directory Tree: Top Health Conditions and Diseases Genetic Disorders : Laurence-Moon Syndrome ( 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.

43. Laurence Moon (Bardet Biedl) Syndrome (LMBBS) Laurence Moon (Bardet Biedl) Syndrome (LMBBS). LaurenceMoon-Bardet-Biedl Network; laurence-moon syndrome; LMBBS Home page; Laurence Moon Bardet Biedl Syndrome; http://www.bdid.com/lmbbs.htm

HOME Laurence Moon (Bardet Biedl) Syndrome (LMBBS) Bardet-Biedl Laurence-Moon Syndroom Laurence-Moon-Bardet-Biedl Syndrome Syndrome de Laurence-Moon-Bardet-Biedl Laurence-Moon-Bardet-Biedl Network ... Laurence-Moon-Bardet-Biedl Syndrome Also see Bardet Biedl Syndrome HOME

44. Bardet-Biedl Laurence-Moon Syndroom/History The estimates for laurencemoon syndrome are much lower still. Learning disabilities. laurence-moon syndrome. * Spasticity (often progressive) or ataxia. http://www.angelfire.com/co3/PEKICH/BBLMS_history.html

var cm_role = "live" var cm_host = "angelfire.lycos.com" var cm_taxid = "/memberembedded" top NL / ENG Bardet-Biedl Laurence-Moon Syndroom Home History Symptoms Treatment Aids Cause ... e-mail T h e Bardet-Biedl and Laurence-Moon syndromes are two uncommon disorders. Both syndromes are genetic, that is, caused by altered genes, and occur throughout the world, equally in men and in women. Historically these conditions were so similar that for some time they had been considered the same disorder. However, in the past few years, it has become apparent that these are two separate and distinct syndromes Brief history I n 1866 doctors Laurence and Moon in England described four members of the same family who had retinal problems, unsteady gait and spinal cord problems, and developmental delays. In the 1920’s Doctors Bardet (in France) and Biedl (in Germany) independently published articles describing patients with extra fingers and toes at birth, infantile obesity, and retinal disorders. The similarities of the signs in these patients were so striking that it was decided to adopt the suggestion to speak of these as one syndrome: Laurence-Moon/Bardet-Biedl Syndrome.

45. Bardet-Biedl Laurence-Moon Syndroom/Treatment BardetBiedl Syndrome and laurence-moon syndrome are incurable. Proper medical treatment and emotional guidance help a patient with either syndrome to cope. http://www.angelfire.com/co3/PEKICH/BBLMS_treatment.html

var cm_role = "live" var cm_host = "angelfire.lycos.com" var cm_taxid = "/memberembedded" top NL / ENG Bardet-Biedl Laurence-Moon Syndroom Home History Symptoms Treatment Aids Cause Parent Contact Group View guestbook ... e-mail Bardet-Biedl Syndrome and Laurence-Moon Syndrome are incurable. Proper medical treatment and emotional guidance help a patient with either syndrome to cope. Below we give some suggestions for certain symptoms related to the syndromes. 1.RETINAL DISORDERS AND NIGHT BLINDNESS R etinal dysfunction is incurable at this time. With that in mind it is essential to use the remaining vision by wearing proper corrective lenses. Regular visits to an ophthalmologist who is skilled in retinal disorders and in refraction are imperative. Emotional and especially practical guidance of children and young adults who are losing their vision is not an easy task. Because of their decreasing vision and night blindness, people with Laurence-Moon or Bardet-Biedl Syndromes benefit from orientation and mobility training and the use of a guide cane.

46. 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

47. Débats Listesnof : Syndrome De Laurence-Moon-Bardet-Biedl Translate this page but that the patients of Laurence and Moon had a distinct disorder with paraplegia and without polydactyly and obesity (see laurence-moon syndrome, 245800). http://www.cocnet.org/snof/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.

48. Mental Retardation, Directory LaurenceMoon-Bardet-Biedl Syndrome, Family Village laurence-moon syndrome, OMIM, Victor A. McKusick BARDET-BIEDL SYNDROME; BBS, OMIM, Victor A. McKusick et al http://www.saunalahti.fi/kup/engl/webs_l.html

Finnish Information Center on Mental Retardation English links A B C D ... Z Lambotte syndrome Lambotte syndrome, OMIM, Victor A. McKusick Private multiple congenital anomaly syndromes may result from unbalanced subtle translocations: t(2q;4p) explains the Lambotte syndrome., Herens C et al, PubMed Lambotte syndrome: microcephaly, holoprosencephaly, intrauterine growth retardation, facial anomalies, and early lethalitya new sublethal multiple congenital anomaly/mental retardation syndrome in four sibs, Verloes A et. al, PubMed Langer-Giedion Syndrome Langer-Giedion Syndrome; LGS, OMIM, Victor A. McKusick Trichorhinophalangeal Syndrome Type II (NORD) Langer Giedion Syndrome Home Page, The University of Houston Langer Giedion Syndrome Association, USA ... Yahoo! Directory Langer-Giedion Syndrome Laurence-Moon-Bardet-Biedl Syndrome Laurence-Moon-Bardet-Biedl Syndrome, Family Village LAURENCE-MOON SYNDROME, OMIM, Victor A. McKusick BARDET-BIEDL SYNDROME; BBS, OMIM, Victor A. McKusick et al. BBS1 GENE; BBS1, OMIM. Victor A. McKusick ... The Laurence-Moon-Bardet-Biedl Society Lennox-Gastaut Syndrome Lennox-Gastaut Syndrome, EPINET, Epilepsy Foundation of Victoria (Australia)

49. The Medword List - Medical Transcription Directory - The Medword List - Conditio pedals smartype and more, search medword. Top Level Conditions and Diseases Genetic Disorders laurencemoon syndrome. Links http://www.medwordlist.com/Conditions_and_Diseases/Genetic_Disorders/Laurence-Mo

Top Level Conditions and Diseases Genetic Disorders : Laurence-Moon Syndrome 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. http://www.lmbbs.org.uk (Added: Mon Jan 01 2001 Hits: 9 Rating: 0.00 Votes: ) Rate It Authentic WAVpedal Foot Pedal WAVpedal allows PC playback of most all digital voice recorder formats. Medword Store Stedman's Smartype Speedtyping software for MTs using MS Word. Increases production and accuracy. Medword Store Handheld Medical Spell Checker ideal for people who may need to verify medical spelling on occassion. Also, CenturionMail e-Mail Security Medword Store Alpha II Coding Software Audio Cassette Tape Eraser CenturionMail HIPAA Compliant E-Mail Encryption Computer Security ... Special Quick Browse Section SuperFast Amazon.com Search Medword Medical Transcription About Medword Contact Medword Customer Care FAQs ... Prevent ID Theft

50. The Foundation Fighting Blindness - Canada Related Syndromes LaurenceMoon-Biedl syndrome is also known as laurence-moon syndrome. In individuals with laurence-moon syndrome http://www.ffb.ca/disease_bardet-biedl.php?hc=1

51. NodeWorks - Genetic Disorders: Laurence-Moon Syndrome Top Health Conditions Diseases Genetic Disorders laurencemoon syndrome ( 3 ). laurence-moon syndrome is a rare inherited http://dir.nodeworks.com/Health/Conditions_and_Diseases/Genetic_Disorders/Lauren

in entire NodeWorks Directory in Health in Genetic Disorders in ++ Laurence-Moon Syndrome Top Health Genetic Disorders Laurence-Moon Syndrome 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). 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. NORD: Laurence Moon Syndrome Offers alternative names, a general discussion and further resources. NodeWorks boosts web surfing! Page Returned in seconds - HTML Compressed Help build the largest human-edited directory on the web.

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

53. FORMULAIRE INSCRIPTION RECHERCHE WWW.LACHAINETTE.COM Contacts Rare disease selected laurencemoon syndrome Id, First name, Country, Web. 795, philippe, FRANCE, http://www.lachainette.com/US/ContactsPathologie.php?Action=contacter&Id=356

54. Congenital, Hereditary, And Neonatal Diseases And Abnormalities The US Nat l Incontinentia Pigmenti Foundation New York. laurence-moon syndrome. Laurence-Moon-Bardet-Biedl Network Home Page M Morris. http://www.mic.ki.se/Diseases/C16.html

search search staff sitemap ABOUT KAROLINSKA INSTITUTET ... print this page Diseases and Disorders Links pertaining to Congenital, Hereditary, and Neonatal Diseases and Abnormalities Alert! Patients and laypersons looking for guidance among the target sources of this collection of links are strongly advised to review the information retrieved with their professional health care provider. Start Page Contents: Abnormalities Aicardi Syndrome (not on MeSH) Amniotic Band Syndrome Anencephaly ... Wolf-Hirschhorn Syndrome (not on MeSH) Congenital, Hereditary, and Neonatal Diseases and Abnormalities The US National Organization for Rare Disorders , including a Rare Disease Database , and a List of Disease-specific Organizations Search Jablonski's MCA/MR Syndromes Database [Congenital Abnormalities associated with Mental Retardation] - NLM (US) Indice delle malattie [in Italian] - InformaGene (IT) A Short History of Mapping [P Murphy] GENATLAS: Pathology Search [J Frezal] - Univ Rene Descartes, Paris (FR) OrphaNet [rare diseases] - (FR) A Birth Disorder Information Directory - Spamgid.com

55. OMIM - LAURENCE-MOON SYNDROME http://www3.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=245800

56. Bardet Biedl Syndrome Confusion exists in the medical literature regarding the difference between BardetBiedl Syndrome and laurence-moon syndrome. . Resources. http://www.meritcare.com/hwdb/showTopic.asp?pd_hwid=nord988

57. Wauu.DE: Health: Conditions And Diseases: Genetic Disorders: Laurence-Moon Syndr http//www.lmbbs.org.uk. National Library of Medicine A look at the former names of laurencemoon syndrome, a summary and a list of clinical features. http://www.wauu.de/Health/Conditions_and_Diseases/Genetic_Disorders/Laurence-Moo

Home Health Conditions and Diseases Genetic Disorders : Laurence-Moon Syndrome Search DMOZ-Verzeichnis: All Categories Categories Onlye 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. http://www.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. 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. http://www.icondata.com/health/pedbase/files/LAURENCE.HTM © 1998- 2002 Ein Service von Wauu.de UserNet.DE Linktip: MnogoSearch.ORG Map TopTen TopTen eng Aktuelle Linktips Mozilla 1.7 RC 1 Basteln 0190 Warner Free Rund ums Rad ... Fantasy - Shop Webmaster-Links Webspace Free Subdomain Service Merchandise Fun SUMA - Forum ... Abmahnungen œber Wauu Regeln Webmasterservice Impressum b

58. Laurence-Moon-Biedl Syndrome » Medical Diagnosis Medical Diagnosis » L » LaurenceMoon-Biedl syndrome. supportive MISCELLANEOUS. SYNONYMS • laurence-moon syndrome • Bardet-Biedl syndrome ICD-9-CM http://www.medfamily.org/diagnosis/L/diagnosis-terms-Laurence_Moon_Biedl_syndrom

Medical Diagnosis A B C ... Z Laurence-Moon-Biedl syndrome Laurence-Moon-Biedl syndrome OVERVIEW: 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: TREATMENT MISCELLANEOUS SYNONYMS: ICD-9-CM: 759.8 Laurence-Moon-Biedl syndrome see images More Helpful Links Want to discuss this term? Visit our forum or our chat room SEE ALSO (Enter the keywords below into our search box or click on the link): n/a Total Medical Terms: Rate this site! 1 - Worst 10 - Best Joint Partnership with Care Earth SGU Community Solo Futbol TUMS-Ped ... Cheap Store We're still here, you rockin' with the best! Best View with 1024x768 screen and IE 5.0 Although the medFamily materials have been developed by physicians and health care provider it is designed for educational purposes only. The site is not engaged in rendering medical advice. The information provided should not be used for diagnosing or treating a health problem or a disease. It is not a substitute for professional care. It is solely for information and second opinion purposes. If you have or suspect you may have a health problem, you should consult your health care provider and use the information here as a cross references. The authors, editors, producers, sponsors, and contributors shall have no liability, obligation or responsibility to any person or entity for any loss, damage, or adverse consequence alleged to have happened directly or indirectly as a consequence of this material.

59. ZapMeta Directory > Health > Conditions And Diseases > Genetic Disorders > Laure Web Sites in Category laurencemoon syndrome Display results 1 - 4 of 4 matches. . NORD Laurence Moon Syndrome open this site in a new window Past Versions http://www.zapmeta.com/search/meta/db.pl?dir=525030

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

DeCS 2000 - Changed terms Replaced Replaced-by ACOUSTIC NERVE VESTIBULOCOCHLEAR NERVE ACOUSTIC NERVE DISEASES VESTIBULOCOCHLEAR NERVE DISEASES ADIE'S SYNDROME ADIE SYNDROME AMYGDALOID BODY AMYGDALA ANDROGEN-BINDING PROTEINS ANDROGEN-BINDING PROTEIN ANOSMIA OLFACTION DISORDERS APRAXIA APRAXIAS ARNOLD-CHIARI DEFORMITY ARNOLD-CHIARI MALFORMATION ASPARTIC PROTEINASES ASPARTIC ENDOPEPTIDASES CALLUS BONY CALLUS CEREBELLAR DYSSYNERGIA MYOCLONIC CEREBELLAR DYSSYNERGIA CEREBRAL ANEURYSM INTRACRANIAL ANEURYSM CEREBRAL ANOXIA HYPOXIA, BRAIN CEREBRAL ARTERIOSCLEROSIS INTRACRANIAL ARTERIOSCLEROSIS CEREBRAL ARTERIOVENOUS MALFORMATIONS INTRACRANIAL ARTERIOVENOUS MALFORMATIONS CEREBRAL ARTERY DISEASES CEREBRAL ARTERIAL DISEASES CEREBRAL EMBOLISM AND THROMBOSIS INTRACRANIAL EMBOLISM AND THROMBOSIS CEREBRAL ISCHEMIA BRAIN ISCHEMIA CEREBRAL ISCHEMIA, TRANSIENT ISCHEMIC ATTACK, TRANSIENT CEREBRAL SCLEROSIS, DIFFUSE DIFFUSE CEREBRAL SCLEROSIS OF SCHILDER CEREBROSPINAL OTORRHEA CEREBROSPINAL FLUID OTORRHEA CEREBROSPINAL RHINORRHEA CEREBROSPINAL FLUID RHINORRHEA CHARCOT-MARIE DISEASE CHARCOT-MARIE-TOOTH DISEASE CHORDATA CHORDATA, NONVERTEBRATE

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