81. Syndrome Of Bardet-Biedl bardetbiedl s syndrome is a hereditary disease that affects many parts of the body . bardet-biedl s syndrome 1, which does not have relation with the http://www.obesidad.net/english2002/disorder9.shtml

Bardet-Biedl's syndrome Health has no price Obesidad.net is educational Visit us continually. You will always find new advice for your health. Recommend this site. Recommend this site to a friend or relative who may find it helpful BARDET-BIEDL'S SYNDROME Bardet-Biedl's syndrome is a hereditary disease that affects many parts of the body. Obesity, the pygmentary retinitis (night blindness and the progressive loss of the peripheral vision), the mental delay, the hypogonadism, the renal damage and the polydactylia (fingers extra in the feet), define the characteristics of Bardet-Biedl's syndrome. INHERITANCE Two forms have been identified: Bardet-Biedl's syndrome 1, which does not have relation with the chromosome 16. Bardet-Biedl's syndrome 2, that has relation with the chromosome 16. Bardet-Biedl's syndrome is transmitted genetically across the families by inheritance autosomic recessive. In this type of inheritance, both parents are called carriers, they have a gene of the syndrome paired with a normal gene. Each of his children have at the time a possibility of 25% (or an opportunity in four) of inheriting both Bardet-Biedl's genes (one of every father) necessary to cause this disease. The carriers are healthy because only they have a copy of the gene. At this moment, it is impossible to determine if someone is a carrier of Bardet-Biedl's syndrome but until the birth of an affected child.

82. Syndrome De Bardet-Biedl : Sites Et Documents Francophones bardet-biedl, syndrome ; syndrome de MacKusick-Kaufmann . Synonyme(s) MeSH syndrome de Laurence Moon Bardet Biedl. http://www.chu-rouen.fr/ssf/pathol/bardetbiedlsyndrome.html

Syndrome de Bardet-Biedl Synonyme(s) CISMeF Bardet-Biedl ; Bardet-Biedl type 1, syndrome de ; Bardet-Biedl type 2, syndrome de ; Bardet-Biedl type 3, syndrome de ; Bardet-Biedl type 4, syndrome de ; bardet-Biedl, syndrome ; syndrome de Mac Kusick-Kaufmann . Synonyme(s) MeSH Syndrome de Laurence Moon Bardet Biedl Arborescence(s) syndrome de Bardet-Biedl bardet-biedl syndrome maladies du système nerveux maladies et malformations congénitales, héréditaires et néonatales 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 Ou consulter ci-dessous une sélection des principales ressources : Qualificatifs : diagnostic guide ressources Bardet-Biedl, syndrome de [Par Pr Bonneau D. Site éditeur Orphanet base de données sur les maladies rares et les médicaments orphelins. Direction Générale de la Santé / INSERM ; ; pays : France ; langue : français ; format : html ; accès : gratuit ; non parrainé ; daté de : 2003 ; visité le : 19/12/2000].

83. ORPHANET - Maladies Rares - Médicaments Orphelins Translate this page bardet-biedl, syndrome de, type 1 bardet-biedl, syndrome de, type 2 Le syndromede bardet-biedl est une maladie génétique autosomique récessive qui http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=110

84. NORD - National Organization For Rare Disorders, Inc. National Organization for Rare Disorders is dedicated to helping people withrare, orphan diseases. Rarediseases.org contains information on the prevention, http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Bardet Biedl

85. Laurence Moon/Bardet Biedl Syndrome Bardet Biedl syndrome bar3.gif (4740 bytes). Condensered.gif (846 bytes) LMBBSHome page This page is aimed primarily at medical and healthcare http://www.lowvision.org/laurence_moon.htm

Laurence Moon/ Bardet Biedl Syndrome LMBBS Home page 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. LMBBS Home page 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.

86. Online And Offline Support: L People served Families dealing with Laurence Moon Bardet Biedl syndrome;Services provided Support and information; Address 124 Lincoln Avenue, http://www.widesmiles.org/support/l.html

L Langer-Giedion Syndrome Langer-Giedion Syndrome Association People served: Individuals and families dealing with Langer-Giedion Syndrome Services provided: Information, public awareness, support for families, newsletter, and advocacy for research Contact people: Raquel Rozenberg Address: 9021 45th Ave. N, Minneapolis MN 55428 Email address: roze0002@umn.edu Louise Kinross 89 Ingham Ave. Toronto, Ont. M4K 2W8, Canada Email address: kinross@istar.ca Email address: lgsa@geocities.com Website: http://www.geocities.com/HotSprings/9308/ Laurence-Moon-Bardet-Biedl Syndrome Please note: Laurence-Moon-Bardet-Biedl Syndrome includes specific facial characteristics that do not require reconstructive surgery. The LMBBS Society (United Kingdom) People served: Families dealing with Laurence-Moon-Biedl Syndrome Services provided: Support and information Address: Spring Grove, Loudhams Wood Lane, Chalfont St Giles Bucks HP8 4AR Phone number: 01494 764924 Laurence Moon Bardet Biedl Syndrome (United States) People served: Families dealing with Laurence Moon Bardet Biedl Syndrome Services provided: Support and information Address: 124 Lincoln Avenue, Purchase NY 10577

87. Researchers Have Discovered That Many People With Bardet-Biedl Syndrome Can't De ? Johns Hopkins researchers have discovered that many people with BardetBiedlsyndrome (BBS), a rare, complex condition marked by an array of seemingly http://www.news-medical.net/?id=4276

88. Search Result For "Laurence-Moon-Bardet- Biedl Syndrome(LMBBS)" NOAH pages containing LaurenceMoon-Bardet- Biedl syndrome(LMBBS) . Displaying 1-5of 338. Retinitis Pigmentosa The Eye Clinic and Retinitis Pigmentosa; http://www.noah-health.org/search/results.php?lang=1&keyword=Laurence-Moon-Barde

89. Wordbank On The Mental Health Foundation Website Bardet Biedl syndrome. spacer. genetic disorder of chromosomes 16, 3, and 15which causes progressive blindness, obesity, extra fingers and toes, http://www.mentalhealth.org.uk/wordbank.cfm?wordid=741&wbletter=B

90. Bardet Biedl Syndrome Bardet Biedl syndrome is a group of rare disorders inherited as autosomalrecessive genetic traits. http://my.webmd.com/hw/raising_a_family/nord988.asp

var guid_source = ""; var guid_source_id = ""; //unused var encodedurl = ""; WebMD Today Home WebMD News Center XML News via RSS Member Services WebMD University My WebMD Find a Physician Medical Info Check Symptoms Medical Library Health Tools Clinical Trials ... Women, Men, Lifestyle Who We Are About WebMD Site Map Health Topics Symptoms ... For a Complete Report Bardet Biedl Syndrome Important It is possible that the main title of the report Bardet Biedl 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 Biedl-Bardet Syndrome Disorder Subdivisions None 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. Resources National Association for Visually Handicapped 22 West 21st Street New York, NY 10010

91. Bardet Biedl Syndrome Articles, Support Groups, And Resources Bardet Biedl syndrome articles, support groups, and resources for patients fromMed Help International (www.medhelp.org) http://www.medhelp.org/HealthTopics/Bardet_Biedl_Syndrome.html

[Health Topics A-Z] A B C D ... Z Bardet Biedl Syndrome Support Groups: Laurence Moon Bardet Biedl Syndrome Med Help International Search Medical Forums / Message Boards ... Site Map Revised: 9/7/2005

92. Birth Disorder Information Directory - BA-BL Bardet Biedl syndrome. List of Sites. Bare Lymphocyte syndrome (Defective Expressionof HLA Class 2, HLA Class 2Negative). List of Sites. Barnes syndrome http://www.bdid.com/defectba.htm

HOME Ba-Bl B-K Mole Syndrome See Melanoma, Familial/Cutaneous Malignant Type Bader Syndrome (Odontomatosis Aortae Oesophagus Stenosis, Odontoma Dysphagia Syndrome) bader syndrome ODONTOMA-DYSPHAGIA SYNDROME BADS Syndrome See Black Locks with Albinism and Deafness Syndrome Baelz Syndrome (Cheilitis Glandularis) baelz syndrome CHEILITIS GLANDULARIS Bagatelle Cassidy Syndrome (Macrocephaly Short Limbs Deafness) bagatelle cassidy syndrome Bahemuka Brown Syndrome (Spastic Paraplegia Facial Cutaneous Lesions) bahemuka brown syndrome Baker Vinters Syndrome (Hydrocephalus Craniosynostosis Bifid Nose) baker vinters syndrome Ballard Syndrome (Brachydactyly, Combined B and E Types; Pitt Williams Brachydactyly) ballard syndrome BRACHYDACTYLY, COMBINED B AND E TYPES Baller Gerold Syndrome See Craniosynostosis-Radial Aplasia Syndrome Ballinger Wallace Syndrome (Diabetes-Deafness Syndrome, Maternally Transmitted; Diabetes Mellitus, Noninsulin-Dependent/Type II, with Deafness) Ballinger-wallace syndrome DIABETES-DEAFNESS SYNDROME, MATERNALLY TRANSMITTED Bamboo Hair Syndrome See Netherton Disease Bamforth Syndrome (Hypothyroidism, Athyroidal, with Spiky Hair and Cleft Palate)

93. Bardet Biedl Syndrome - St. Joseph Mercy, Ann Arbor Michigan Bardet Biedl syndrome St. Joseph Mercy Health System Hospitals serving AnnArbor, SE Michigan, Washtenaw County, Livingston County, Wayne County, http://www.sjmercyhealth.org/12648.cfm

@import url(default.css); Online Health Information Health Information - Rare Diseases and Disorders Back to Health Library Print This Page Email to a Friend National Organization for Rare Disorders, Inc. Bardet Biedl Syndrome Synonyms Disorder Subdivisions General Discussion Resources ... For a Complete Report Important It is possible that the main title of the report Bardet Biedl 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 Biedl-Bardet Syndrome Disorder Subdivisions None 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. Resources National Association for Visually Handicapped 22 West 21st Street New York, NY 10010

94. Hill Health Topics A-Z - Bardet Biedl Syndrome Bardet Biedl syndrome. National Organization for Rare Disorders. Important It ispossible that the main title of the report Bardet Biedl syndrome is not the http://www.healthwise.net/hillhealth/Content/StdDocument.aspx?DOCHWID=nord988&SE

95. Bardet Biedl Syndrome Complete online version of The Encyclopaedia of Medical Imaging including textand images from The Encyclopaedia of Medical Imaging s eight book volumes http://www.amershamhealth.com/medcyclopaedia/medical/Volume VII/BARDET BIEDL SY

financial services our commitment our company Search Medcyclopaedia for: Search marked text (mark text before you click) Browse entry words starting with: A B C D ... amershamhealth.com Bardet biedl syndrome, (Georges Bardet, born 1885, French physician; Artur Biedl, 18691933, Austrian physician), this shares with Laurence Moon Biedl syndrome pigmented retinopathy, hypogonadism and renal tract abnormalities but also involves polydactyly. Inheritance is autosomal recessive. Radiology: polydactyly and urinary tract anomalies cysts, and small or large echogenic kidneys. HC The Encyclopaedia of Medical Imaging Volume VII Corporate Products Financial Services Our Commitment ... Terms of Conditions

96. Many People With Bardet Biedl Syndrome Cannot Detect Smells Johns Hopkins researchers have discovered that many people with BardetBiedlsyndrome (BBS), a rare, complex condition marked by an array of seemingly http://www.medicalnewstoday.com/medicalnews.php?newsid=12429

97. Bardet Biedl Syndrome Synonyms, Eastern Carolina Bardet Biedl syndrome Synonyms University Health Systems of Eastern Carolinaserves tarboro, ahoskie, edento, winsor, maxhead, dear county, http://www.uhseast.com/112057.cfm

Health News Health Library Health Topics Healthy Living ... Nutrition Information on diseases and health concerns, including symptoms, treatment options, and prevention. Bardet Biedl Syndrome Synonyms Disorder Subdivisions General Discussion Resources ... For a Complete Report Important It is possible that the main title of the report Bardet Biedl 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 Biedl-Bardet Syndrome Disorder Subdivisions None 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. Resources National Association for Visually Handicapped 22 West 21st Street New York, NY 10010

98. Laurence Moon Bardet Biedl Syndrome - Patient UK They have not been checked to see if Laurence Moon Bardet Biedl syndrome isincluded but these large sites are comprehensive. NonUK disease / illness sites http://www.patient.co.uk/showdoc/401/

Laurence Moon Bardet Biedl Syndrome UK sources of information and / or support Laurence Moon Bardet Biedl Society Support and information for families affected by LMBB syndrome. Further sources / More detailed information Some non-UK sites The following list popular non-UK health information sites, mainly from the US. They have not been checked to see if Laurence Moon Bardet Biedl syndrome is included but these large sites are comprehensive. Non-UK disease / illness sites Non-UK self-help / support group sites Evidence Based Medicine For sites and information on Evidence Based Medicine. Searching Medline For information on Medline and how it is used to find detailed medical and health information. Sponsored links and adverts Patient UK has no control of the content of the following links. Inclusion does not imply endorsement by Patient UK. Health Related Books From Amazon - browse hundreds of books on health and disease. Also, worth a look... Related pages in Patient UK Patient Plus Bardet-Biedl Syndrome Other - Useful resources Pictures, diagrams, photos, images, etc.

99. Bardet Biedel Syndrome The Bardet Biedl syndrome is an autosomal recessive disorder In late 1993,we mapped the first gene for Bardet Biedl syndrome to the long arm of http://www.ophth.uiowa.edu/BBS.html

Hereditary Obesity - Bardet Biedl Syndrome The Bardet Biedl syndrome is an autosomal recessive disorder characterized by obesity, retinal degeneration, extra digits on the hands and feet, and mental retardation. Just as identifying the genes for early-onset, hereditary forms of macular degeneration and glaucoma may provide clues to the more common late-onset forms of these diseases, we are hopeful that the identification of a gene for Bardet Biedl Syndrome will provide important insight into the common forms of pathological human obesity. Extra digits and obesity are two of the cardinal features of Bardet Biedl Syndrome. In late 1993, we mapped the first gene for Bardet Biedl syndrome to the long arm of chromosome 16 by studying a large inbred family from Israel. In 1994, we mapped two other genes for this disorder to chromosomes 3, and 15 in additional Bedouin families from Israel. We have also developed a new technique for gene mapping in inbred families that significantly reduces the time required to find the chromosomal location of a gene. We are currently applying this new method to a variety of different recessive diseases. Highly polymorphic genetic markers are used to identify the chromosomal location of disease-causing genes.

100. Healthfinder® — Laurence Moon Bardet Biedl Syndrome Information And Referral S Links to support services, organizations, genetic societies, treatment clinicsand other resources related to Laurence Moon Bardet Biedl syndrome. http://www.healthfinder.gov/Scripts/ShowDocDetail.asp?doc=4525&lang=1

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