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
Extractions: 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.
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
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
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
Extractions: 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.
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
Extractions: L Langer-Giedion Syndrome Langer-Giedion Syndrome Association Louise Kinross 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) 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
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
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
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
Extractions: 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.
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
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Extractions: 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. 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. National Association for Visually Handicapped
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
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
Extractions: 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.
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
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
Extractions: 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. 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. National Association for Visually Handicapped
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/
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
Extractions: 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.
