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         Bardet-biedl Syndrome:     more detail
  1. Biochemists focus on BBS.(Michel Leroux and Oliver Blacque's research on Bardet-Biedl Syndrome ): An article from: Canadian Chemical News
  2. Bardet-Biedl Syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Avis Gibons, 2005
  3. Maladie Du Segment Postérieur: Dégénérescence Maculaire Liée à L'âge, Uvéite, Syndrome de Bardet-Biedl, Rétinite Pigmentaire (French Edition)
  4. The (Laurence Moon) Bardet Biedl syndrome (Van Gorcum's medical collection, no. 207) by W Stiggelbout, 1969

1. Bardet-Biedl Syndrome (BBS)
A summary of bardetbiedl syndrome and a list of major features.
http://www.nlm.nih.gov/mesh/jablonski/syndromes/syndrome048.html
Multiple Congenital Anomaly/Mental Retardation (MCA/MR) Syndromes
View the Full Record
Syndrome Bardet-Biedl syndrome (BBS) Summary A syndrome characterized mainly by obesity, pigmentary retinopathy, polydactyly, mental retardation, hypogonadism, and renal failure in fatal cases. Two forms have been identified: Bardet-Biedl syndrome 1 (BBS1) has no linkage to chromosome 16 Bardet-Biedl syndrome 2 (BBS2) is mapped to markers on chromosome 16. Laurence-Moon-Biedl syndrome and Laurence-Moon-Biedl-Bardet syndrome are no longer considered as valid terms in that patients of Laurence and Moon had paraplegia but no polydactyly and obesity which are the key elements of the Bardet-Biedl the syndrome. Laurence-Moon syndrome is a separate entity. Major Features Eyes: Pigmentary retinopathy. Hand and foot: Polydactyly. Cardiovascular system: Hypertrophy of interventricular septum and left ventricle and dilated cardiomyopathy. Gastrointestinal system: Fibrosis. Urogenital system: Hypogonadism, renal failure, urogenital sinuses, ectopic urethra, uterus duplex, septate vagina, and hypoplasia of the uterus, ovaries, and fallopian tubes. Growth and development: Mental and growth retardation.

2. BARDET-BIEDL SYNDROME : Contact A Family - For Families With Disabled Children:
Information about Laurencemoon-bardet-biedl syndrome, its symptoms and inheritance patterns.
http://www.cafamily.org.uk/Direct/b10.html
printer friendly BARDET-BIEDL SYNDROME home how we can help medical information index of conditions ... how you can help Did you find this page
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yes no Bardet-Biedl syndrome: BBS; Laurence-Moon-Bardet-Biedl syndrome The syndrome is a rare inherited condition which is variable in the way in which it presents. Characteristics are rod/cone dystrophy (atypical retinitis pigmentosa - a progressive eye condition which can lead to blindness (see Visual Impairment )); obesity (usually with an early onset and resistant to treatment); polydactyly (extra fingers and/or toes); hypogenitalism (underdeveloped genitals); mild to severe learning difficulties. Usually four out of these five features are required to make the diagnosis. In addition, there are other important characteristics which need to be taken into account: kidney malformations and renal dysfunction; developmental delay; speech difficulties; diabetes mellitus and, rarely, diabetes insipidus; hepatic fibrosis and other hormonal deficiencies. In the Middle-East and island communities such as Newfoundland, the condition is relatively common, occurring at rates of 1 in 13,500 of the population. In Europe and the UK the prevalence is much less common owing to lower consanguinity. The figure is probably around 1 in 100,000 of the population. Although BBS is not common it is certainly under diagnosed. As awareness of the condition increases, the number of people identified is growing every year.

3. Bardet-Biedl Syndrome (BBS)
A summary of bardetbiedl syndrome and a list of major features.
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

4. Www.nlm.nih.gov/cgi/mesh/2K/MB_cgi?term=Bardet-Bie
Laurence Moon Bardet Biedl SyndromeLauurence Moon Bardet Biedl Syndrome Resources, international support groups,clinics, genetic counselors and geneticists.
http://www.nlm.nih.gov/cgi/mesh/2K/MB_cgi?term=Bardet-Biedl Syndrome

5. Reader's Digest - Rd.com:  Health & Wellness
bardetbiedl syndrome General information and resources.
http://www.readersdigesthealth.com/kbase/nord/nord988.htm
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6. 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

7. 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

8. NORD - National Organization For Rare Disorders, Inc.
the difference between LaurenceMoon Syndrome and bardet-biedl syndrome.Some researchers believe that bardet-biedl syndrome is a subdivision of
http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Laurence Moon

9. BARDET-BIEDL SYNDROME Contact A Family - For Families With
Information about Laurencemoon-bardet-biedl syndrome, its symptoms and inheritance patterns.
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

10. Clinical Trial: Genetics And Clinical Characteristics Of Bardet-Biedl Syndrome
Patients with bardetbiedl syndrome may be eligible for this study. Although bardet-biedl syndrome (BBS) was described more than 80 years ago,
http://www.clinicaltrials.gov/ct/show/NCT00078091
Home Search Browse Resources ... About Genetics and Clinical Characteristics of Bardet-Biedl Syndrome This study is currently recruiting patients.
Verified by National Institutes of Health Clinical Center (CC) November 30, 2004 Sponsored by: National Human Genome Research Institute (NHGRI) Information provided by: National Institutes of Health Clinical Center (CC) ClinicalTrials.gov Identifier: Purpose This study will evaluate patients with a rare inherited condition called Bardet-Biedl syndrome . The purpose of the study is to learn more about the genetics and clinical characteristics of this disorder. Patients may have the following problems: polydactyly (extra fingers and toes); retinal dystrophy (changes in the retina that may lead to vision problems, including blindness); obesity and diabetes (overweight and high blood sugar due to failure of body organs to respond to insulin); cognitive dysfunction (difficulties with learning and understanding); hypogenitalism (decreased functioning of the ovaries in women and the testes in men); kidney anomalies (changes in the structure or function of the kidneys); heart disease; and hepatic fibrosis (liver disease). Patients with Bardet-Biedl syndrome may be eligible for this study. First-degree relatives will also be enrolled for certain tests and procedures. Candidates are screened with a review of their medical records, laboratory tests, and x-rays.

11. 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

12. National Neurovision Research Institute Click Here For More
bardetbiedl syndrome is a complex disorder that affects many parts of the body The diagnosis of bardet-biedl syndrome is usually confirmed in childhood
http://www.blindness.org/visiondisorders/causes.asp?type=27

13. Laurence Moon (Bardet Biedl) Syndrome (LMBBS)
Laurence Moon (Bardet Biedl) Syndrome (LMBBS) BardetBiedl Laurence-Moon Syndroom Laurence-Moon-bardet-biedl syndrome
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

14. Laurence-Moon-Bardet-Biedl Syndrome / Family Village Library
Who to Contact * Where to Go to Chat with Others * Learn More About It * WebSites * Search Google for Laurence Moon Bardet Biedl Syndrome
http://www.familyvillage.wisc.edu/lib_lmbb.htm
Laurence-Moon-Bardet-Biedl Syndrome
Who to Contact
Where to Go to Chat with Others

Learn More About It

Web Sites
...
Search Google for "Laurence Moon Bardet Biedl Syndrome"
Who to Contact
Laurence-Moon-Bardet-Biedl Syndrome Network
c/o Mary Morris
15205 W. Port Royale Lane Ave
Surprise, AZ 85379
E-mail: josiahsmom@hotmail.com
Web: http://mlmorris.com/lmbbs/
Where to Go to Chat with Others
  • LMBBS
    An e-mail discussion list for people affected by Laurence Moon / Bardet Biedl Syndrome and their families and friends.
Learn More About It
Web Sites
Back to [ K - L Family Village Home Library Coffee Shop ... Information Last Updated 1/21/2004 by familyvillage@waisman.wisc.edu Document Source: http://www.familyvillage.wisc.edu/lib_lmbb.htm

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

16. The Foundation Fighting Blindess - Bardet-Biedl Syndrome
bardetbiedl syndrome is a rare, inherited disorder that causes a number of In bardet-biedl syndrome, central vision may become blurry as the first
http://www.ffb.ca/disease_bardet-biedl.php?hc=0

17. Clinical Trial Genetics And Clinical Characteristics Of
What's New About Genetics and Clinical Characteristics of bardetbiedl syndrome This study is currently recruiting patients. Sponsored by
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

18. Bardet-Biedl Syndrome - The Foundation Fighting Blindness - Canada
You are in the Diseases section on the bardetbiedl syndrome page. What isbardet-biedl syndrome? bardet-biedl syndrome is a rare, inherited disorder that
http://www.ffb.ca/disease_bardet-biedl-txt.html

19. Cellular Problems Found Behind Complex Obesity Syndrome
bardetbiedl syndrome (BBS), characterized by obesity, learning disabilities and eye and kidney problems, is caused by genetic mutations in the BBS
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

20. Exploring The Molecular Basis Of Bardet-Biedl Syndrome Katsanis
Exploring the molecular basis of bardetbiedl syndrome Nicholas Katsanis1 + , James R. Lupski1 2 3 and Philip L. Beales4
http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

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