41. Laurence-moon, Syndrome : Sites Et Documents Francophones Translate this page laurence-moon, syndrome. Menu général CISMeF. Arborescence(s) du thesaurus MeSHcontenant le mot-clé laurence-moon, syndrome Laurence Moon syndrome http://www.chu-rouen.fr/ssf/pathol/laurencemoonsyndrome.html

Laurence-moon, Syndrome Menu général CISMeF Arborescence(s) Laurence-Moon, syndrome Laurence Moon syndrome maladies et malformations congénitales, héréditaires et néonatales système nerveux, maladies Position du mot-clé dans l' (les) arborescence(s) : Vous pouvez consulter toutes les ressources ou seulement les principales ou utiliser l' outil de recherche les recommandations les documents concernant l' enseignement les documents destinés aux patients 20 janvier 2003 courriel Menu général CISMeF Haut de page © CHU de Rouen . Toute utilisation partielle ou totale de ce document doit mentionner la source.

42. Health Library: All Topics: L: Laurence-Moon-Biedl Syndrome - Healthfinder® Laurence Moon syndrome Basic consumer information about Laurence Moon syndromeincluding a list of synonyms and resources where you can get additional http://www.healthfinder.gov/Scripts/SearchContext.asp?topic=485

43. Special Child: Disorder Zone Archives - Laurence-Moon-Bardet-Biedl Syndrome laurencemoon-Bardet-Biedl syndrome Sabrina Parker. For more information on laurence-moon-Bardet-Biedlsyndrome, please see the following references http://www.specialchild.com/archives/dz-035.html

Disorder Zone Archives Laurence-Moon-Bardet-Biedl Syndrome Sabrina Parker Introduction Laurence-Moon-Bardet-Biedl syndrome (LMBBS) is an autosomal recessive genetic disorder characterized by obesity, retinal degeneration, extra digits on the hands and feet, and intellectual impairment. In an autosomal recessive disorder, both parents must be carriers of the defective gene and both must pass on the defect to the child in order for the child to be affected. If both parents carry the defective gene responsible for causing LMBBS, they have a 1 in 4 chance of having a child with the syndrome. In 1993, the gene responsible for LMBBS was located on chromosome 16q21 (type 2). Shortly thereafter, another gene on chromosome 11q13 (type 1) was identified. Since then, two others were found on chromosomes 3p12 (type 3) and 15q22 (type 4). The most common form of LMBBS is type 1 and the most rare form is type 3. It is expected, however, that another gene that causes the syndrome also exists because there are identified cases that have none of these four defects. The occurrence rate varies in different parts of the world. In regions such as Kuwait, the occurrence is 1 in 13,500 due to a high frequency of inter-family marriages. British studies, on the other hand, show the prevalence to be 1 in 160,000. While this syndrome is considered rare, it is suspected that there is a major problem with under-diagnosis. Features and Characteristics Following is a list of characteristics that have been seen in children with LMBBS. Not all children will exhibit all of these features:

44. Special Child: Disorder Zone Archives syndrome Fragile X syndrome Hydrocephalus Kabuki syndrome Klinefelter syndromeLandauKleffner syndrome, laurence-moon-Bardet-Biedl syndrome Lennox-Gastaut http://www.specialchild.com/disorder.html

Disorder Zone Archives Angelman Syndrome Apert Syndrome Arthrogryposis Multiplex Congenita Asperger Syndrome ... Williams Syndrome The Disorder Zone has been created for educational purposes only and is not intended to serve as medical advice. The information provided in The Zone should not be used for diagnosing or treating a health problem or disease. It is not a substitute for professional care. If your child has any health concerns, please consult your health care provider. Welcome Editor's Note Success Stories Horror Stories ... The Resource Foundation for Children with Challenges By using Special Child and related services, you agree to abide by the terms and conditions

45. Health Information Resource Database: Laurence-Moon-Biedl Syndrome Network Services.. laurencemoon-Biedl syndrome Network. Contact Information.Sonya Coster 124 Lincoln Ave Purchase, NY 10577. 914-251-1163 (Voice). http://www.health.gov/nhic/NHICScripts/Entry.cfm?HRCode=HR3176

46. Database Search Results Database Search Results. Searched keywords for laurencemoon-Biedlsyndrome. laurence-moon-Biedl syndrome Network. NHIC Home Page http://www.health.gov/nhic/NHICScripts/Hitlist.cfm?Keyword=Laurence-Moon-Biedl S

47. Laurence-Moon-Bardet-Biedl Syndrome. Clinical, Title laurencemoon-Bardet-Biedl syndrome. 3. Riise R, Tornqvist K, Lofterød B,Heiberg A, Knudtzon J. Growth in the laurence-moon-Bardet-Biedl syndrome. http://eprints.lub.lu.se/archive/00009672/

48. BARDET-BIEDL (LAURENCE-MOON-BARDET-BIEDL) SYNDROME Features Listed For BARDETBIEDL (laurence-moon-BARDET-BIEDL) syndrome.McKusick 209900. Abnormal liver (including function); Biliary http://www.hgmp.mrc.ac.uk/dhmhd-bin/hum-look-up?154

49. 1Up Health > Health Links Directory > Conditions And Diseases: Genetic Disorders National Library of Medicine A look at the former names of LaurenceMoonsyndrome, a summary and a list of clinical features. NORD http://www.1uphealth.com/links/genetic-disorders-laurence-moon-syndrome.html

Home Contact Us Privacy Caring For Your Well Being Alternative Medicine Clinical Trials Health News Poisons ... Health Topics A-Z Search 1Up Health Health Directory Addictions Alternative Animal ... Weight Loss By Demography Child Health Teen Health Men's Health Women's Health ... Genetic Disorders : Laurence-Moon Syndrome Description See Related Categories Health: Conditions and Diseases: Neurological Disorders: Brain Diseases Health: Conditions and Diseases: Rare Disorders 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. 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. Help build the largest human-edited directory on the web.

50. 1Up Health > Health Links Directory > Conditions And Diseases: Neurological Diso Network Raises public awareness of the laurencemoon Bardet-Biedl syndrome andserves as a place for parents of LMBBS children to meet and exchange ideas. http://www.1uphealth.com/links/brain-diseases-bardet-biedl-syndrome.html

Home Contact Us Privacy Caring For Your Well Being Alternative Medicine Clinical Trials Health News Poisons ... Health Topics A-Z Search 1Up Health Health Directory Addictions Alternative Animal ... Weight Loss By Demography Child Health Teen Health Men's Health Women's Health ... Brain Diseases : Bardet-Biedl Syndrome Description See Related Categories Health: Conditions and Diseases: Genetic Disorders Health: Conditions and Diseases: Rare Disorders Sites The CaF Directory Information about Laurence-moon-bardet-biedl syndrome, its symptoms and inheritance patterns. Laurence-Moon-Bardet-Biedl Syndrome Network Raises public awareness of the Laurence-Moon Bardet-Biedl syndrome and serves as a place for parents of LMBBS children to meet and exchange ideas. National Library of Medicine A summary of Bardet-Biedl syndrome and a list of major features. NORD - Bardet Biedl Syndrome Offers a general discussion along with further resources. Readers Digest Health Bardet-Biedl syndrome: General information and resources. UMDS: LMBBS Information for health-care professionals involved in the care of Laurence-Moon-Bardet-Biedl Syndrome patients and for parents or relatives seeking education on the syndrome.

51. Sindrome Laurence Moon Bardet Biedl Syndrome Bambi Sindrome di Laurence Moon Bardet Biedl Laurence Moon Bardet Biedl http//www.rpitalia.org/riabilitazione_sanpaolo.htmhttp//www.5mcc.com/SUMMARY/0519.html http http://fastnet.it/enti/bambi/sindrome-laurence-moon-bardet-biedl.htm

Sindrome di Laurence Moon Bardet Biedl Laurence Moon Bardet Biedl http://www.rpitalia.org/riabilitazione_sanpaolo.htm http://www.5mcc.com/SUMMARY/0519.html http://www.lmbbs.org.uk http://home.talkcity.com/OceanBlvd/iamahawkfan/bardetbeidlsyndrome.html ... http://rarediseases.about.com/health/rarediseases/cs/bardetbiedlsynd/index.h tm http://www.patient.co.uk/illness/l/laurence_moon_bbs.html http://hjem.get2net.dk/ole_jorgensen http://www.healthfinder.gov/text/docs/doc04525.htm http://www.laurushealth.com/Library/HealthGuide/SelfHelp/_followlink.asp?sgm ... http://www.bis.med.jhmi.edu/Dan/kidbase/bardetbiedl/bardetbiedl-help.html BAMBI -INFORMAZIONI SULLE MALATTIE RARE DEI BAMBINI- E' ON LINE DAL 1997 E-mail ruffelli@tin.it

52. Laurence-Moon-Biedl Syndrome laurencemoon-Biedl syndrome. Usual course - progressive. SYNONYMS laurence-moonsyndrome; Bardet-Biedl syndrome. CAUSES genetic. TREATMENT http://www.5mcc.com/Assets/SUMMARY/0519.html

53. RNIB Research Library Bibliography - Retinitis Pigmentosa (Including Laurence-Mo CUNLIFFE, W. The laurencemoon-Biedl syndrome. RUNGE, P. and others. Histopathologyof mitochondrial cytopathy and the laurence-moon-Biedl syndrome. http://www.rnib.org.uk/wesupply/fctsheet/rpig.htm

Search RNIB site for: RNIB Research Library Bibliography Retinitis Pigmentosa (Including Laurence-Moon-Bardet-Biedl Syndrome): a select bibliography for the layman ARDEN, G. What is retinitis pigmentosa? Talking Sense , Winter 1986, BAIO, E. Young people with R.P. (retinitis pigmentosa): a short talk delivered at the branch chairmen's meeting of the British Retinitis Pigmentosa Society held in London on 24th April 1983. Dublin: RP Ireland - Fighting Blindness, 1983. Unpaged (18pp.). BARRON, S. Psychological problems of retinitis pigmentosa: [paper] presented at the third annual workshop of the National Retinitis Pigmentosa Foundation, New York, October 4, 1975. Dover, DE: The Author, 1975. 15pp. BAUSERMAN, C.M. Orientation and mobility for the retinitis pigmentosa student. Roanoke, VA: The Author, 1980. 18pp. Typescript. BERGSMA, D.R. Ophthalmologic aspects of Usher's syndrome. Baltimore, MD: National Retinitis Pigmentosa Foundation, n.d. [c.1973]. 9pp. BERSON, E.L. Retinitis pigmentosa: early diagnosis and some aspects of prevention.

54. Laurence-Moon-Biedl Syndrome - General Practice Notebook Notebook. laurencemoon-Biedl syndrome. laurence-moon-Biedl syndromeis an autosomal recessive condition characterised by mental http://www.gpnotebook.co.uk/cache/-1898971129.htm

Laurence-Moon-Biedl syndrome Laurence-Moon-Biedl syndrome is an autosomal recessive condition characterised by: mental retardation retinitis pigmentosa hypogonadism spastic paraplegia obesity polydactyly cataract squint renal anomalies (calyceal cysts, clubbing or diverticula; fetal lobulation) Click here for more information...

55. HONselect - Bardet-Biedl Syndrome English BardetBiedl syndrome, - laurence-moon-Bardet-Biedl syndrome - BardetBiedl syndrome - Laurence Moon Bardet Biedl syndrome - syndrome, Bardet-Biedl http://www.hon.ch/HONselect/RareDiseases/C10.228.140.617.200.html

56. NEJM -- The Spectrum Of Renal Disease In Laurence-Moon-Biedl Syndrome The spectrum of renal disease in laurencemoon-Biedl syndrome JD Harnett, JS Green,BC Cramer, G Johnson, L Chafe, P McManamon, NR Farid, W Pryse-Phillips, and http://content.nejm.org/cgi/content/short/319/10/615

HOME SEARCH CURRENT ISSUE PAST ISSUES ... HELP Previous Volume 319:615-618 September 8, 1988 Number 10 Next The spectrum of renal disease in Laurence-Moon-Biedl syndrome JD Harnett, JS Green, BC Cramer, G Johnson, L Chafe, P McManamon, NR Farid, W Pryse-Phillips, and PS Parfrey Table of Contents Find Similar Articles in the Journal Notify a friend about this article Add to Personal Archive ... Related Articles in Medline Articles in Medline by Author: Harnett, J. D. Parfrey, P. S. Medline Citation Abstract Source Information Department of Medicine, Memorial University of Newfoundland, St. John's, Canada. This article has been cited by other articles: Riise, R., Tornqvist, K., Wright, A. F., Mykytyn, K., Sheffield, V. C. (2002). The Phenotype in Norwegian Patients With Bardet-Biedl Syndrome With Mutations in the BBS4 Gene. Arch Ophthalmol [Abstract] [Full Text] WARBURG, M., RIISE, R., BEALES, P., FLINTER, F. (2000). Bardet-Biedl and Cohen syndromes: differential diagnostic criteria. J. Med. Genet. [Full Text] Beales, P. L., Reid, H. A.S., Griffiths, M. H., Maher, E. R., Flinter, F. A., Woolf, A. S. (2000). Renal cancer and malformations in relatives of patients with Bardet-Biedl syndrome. Nephrol Dial Transplant [Abstract] [Full Text] David, A., Bitoun, P., Lacombe, D., Lambert, J.-C., Nivelon, A., Vigneron, J., Verloes, A. (1999). Hydrometrocolpos and polydactyly: a common neonatal presentation of Bardet-Biedl and McKusick-Kaufman syndromes.

57. NEJM -- The Cardinal Manifestations Of Bardet-Biedl Syndrome, A Form Of Laurence The cardinal manifestations of BardetBiedl syndrome, a form of laurence-moon-Biedlsyndrome JS Green, PS Parfrey, JD Harnett, NR Farid, BC Cramer, G Johnson http://content.nejm.org/cgi/content/short/321/15/1002

HOME SEARCH CURRENT ISSUE PAST ISSUES ... HELP Previous Volume 321:1002-1009 October 12, 1989 Number 15 Next The cardinal manifestations of Bardet-Biedl syndrome, a form of Laurence-Moon-Biedl syndrome JS Green, PS Parfrey, JD Harnett, NR Farid, BC Cramer, G Johnson, O Heath, PJ McManamon, E O'Leary, and W Pryse-Phillips Table of Contents Find Similar Articles in the Journal Notify a friend about this article Add to Personal Archive ... Related Articles in Medline Articles in Medline by Author: Green, J. S. Pryse-Phillips, W. Medline Citation Abstract Source Information Department of Community Medicine, Memorial University, St. John's, Newfoundland, Canada. This article has been cited by other articles: Barnett, S, Reilly, S, Carr, L, Ojo, I, Beales, P L, Charman, T (2002). Behavioural phenotype of Bardet-Biedl syndrome. J. Med. Genet. [Full Text] Magen, D., Ish-Shalom, N., Lorber, A., Khoury, A., Zelikovic, I. (2002). An infant with polydactyly and renal anomalies: early diagnosis of a rare syndrome. Nephrol Dial Transplant [Full Text] Katsanis, N., Lupski, J. R., Beales, P. L. (2001). Exploring the molecular basis of Bardet-Biedl syndrome.

58. Laurence-Moon-Bardet-Beidel What is laurencemoon-Bardet-Biedl syndrome? Retinitis Pigmentosa (Including laurence-moon-Bardet-Biedlsyndrome) a select bibliography for the layman . http://www.nhbvi.com/internet/Eye/lmbb.html

Search: What is Laurence-Moon-Bardet-Biedl Syndrome? Information from Contact a Family Information from Guy's Hospital, London Information from the OMIM database Discussion, Publications, and Support Laurence-Moon-Bardet-Biedl Network Laurence-Moon-Bardet-Biedl Society (UK) "Retinitis Pigmentosa (Including Laurence-Moon-Bardet-Biedl Syndrome): a select bibliography for the layman" Link Lists Birth Disorder Information Directory Family Village LowVision.org Sindrome di Laurence-Moon-Bardet-Biedl

59. Orthoguide.com Laurence-Moon-Biedl Syndrome Search results for laurencemoon-Biedl syndrome . NO MATCHES FOUND-Pleaseselect a different keyword or category OR Search AltaVista http://www.orthoguide.com/ortho/Laurence-Moon-Biedl_Syndrome.php3

Search results for "Laurence-Moon-Biedl Syndrome" NO MATCHES FOUND-Please select a different keyword or category OR Search AltaVista for 'Laurence-Moon-Biedl Syndrome' Global Search Add Url Free Medline ... Search Enter Keywords to Search and Your Choice of Search Arguments Or And Match entire phrase Orthoguide.com

60. Lund University, Doctoral Dissertation Title and subtitle laurencemoon-Bardet-Biedl syndrome. Keywords laurence-moon-Bardet-Biedlsyndrome, Alström syndrome, Bardet-Biedl syndrome. http://www.lub.lu.se/cgi-bin/show_diss.pl?db=global&fname=med_81.html

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