Extractions: Bardet-Biedl Syndrome,Laurence-Moon/Bardet-Biedl,Biedl-Bardet,Adipogenital Retinitis Pigmentosa Polydactyly,Adreno-Retinitis Pigmentosa-Polydactyly Syndrome,Bardet-Biedl Syndrome,Laurence-Moon/Bardet-Biedl,Biedl-Bardet,Adipogenital Retinitis Pigmentosa Polydactyly,Adreno-Retinitis Pigmentosa-Polydactyly Syndrome For Information on Workshops and Seminars for Special Needs Children click here The GAPS INDEX Bardet-Biedl Syndrome is a rare disorder inherited as an autosomal recessive genetic trait. Major symptoms of this disorder may include mental retardation, obesity, delayed sexual development or underdeveloped reproductive organs, degeneration of the retinas of the eyes, kidney abnormalities and/or abnormal fingers and/or toes.
Laurence-Moon Syndrome Ailment Name laurencemoon syndrome. Join this Community get help by emailing and chatting to others, and sharing information and experiences, http://www.thirdaid.com/conditions/Laurence-Moon_Syndrome.htm
Extractions: Registration (Details given below are only for use in the Community and under no circumstances is your information ever provided to other 3rd parties. Required Information How would you like to be known? Birthdate: document.RegistrationForm.birthdate_day.options[birthdate_current_Day].selected=true; January February March April May June July August September October November December document.RegistrationForm.birthdate_month.options[birthdate_current_Month].selected=true; E-mail: (confidential) you will not be able to access this site. You are a ... Sufferer Carer Doctor For how long? year(s) State/Province/City: Country: Select a Country Afghanistan Albania Algeria American Samoa Andorra Angola Anguilla Antarctica Antigua And Barbuda Argentina Armenia Aruba Australia Austria Azerbaijan Bahamas Bahrain Bangladesh Barbados Belarus Belgium Belize Benin Bermuda Bhutan Bolivia Bosnia and Herzegovina Botswana Bouvet Island Brazil British Indian Ocean Territory Brunei Bulgaria Burkina Faso Burundi Cambodia Cameroon Canada Cape Verde Cayman Islands Central African Republic Chad Chile China Christmas Island Cocos (Keeling) Islands Columbia Comoros Congo Cook Islands Costa Rica Cote DnullIvoire (Ivory Coast) Croatia (Hrvatska) Cuba Cyprus Czech Republic D.P.R. Korea
Genetic Disorders: Laurence-Moon Syndrome Genetic Disorders laurencemoon syndrome. Opinions, news, views, research, updates National Library of Medicine laurence-moon syndrome. http://www.puredirectory.com/Health/Conditions-and-Diseases/Genetic-Disorders/La
Health, Conditions And Diseases, Genetic Disorders: Laurence-Moon Syndrome laurencemoon syndrome is a rare inherited disorder characterized by diminished hormone production by the testes or ovaries (hypogonadism), progressive loss of http://www.combose.com/Health/Conditions_and_Diseases/Genetic_Disorders/Laurence
Extractions: Related links of interest: 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). Help build the largest human-edited directory on the web.
ORPHANET - Rare Diseases - Orphan Drugs DISEASE laurencemoon syndrome, ICD Q87.8, laurence-moon syndrome is more frequent in the Arab population of Kuwait. * author S. Aymé MD (September. 2001) *, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=2377
:: Ez2Find :: Laurence-Moon Syndrome Guide laurencemoon syndrome, Global Metasearch Any Language Guides, laurence-moon syndrome. ez2Find Home Directory Health Conditions http://ez2find.com/cgi-bin/directory/meta/search.pl/Health/Conditions_and_Diseas
Extractions: Any Language English Afrikaans Arabic Bahasa Melayu Belarusian Bulgarian Catala Chinese Simplified Chinese Traditional Cymraeg Czech Dansk Deutsch Eesti Espanol Euskara Faroese Francais Frysk Galego Greek Hebrew Hrvatski Indonesia Islenska Italiano Japanese Korean Latvian Lietuviu Lingua Latina Magyar Netherlands Norsk Polska Portugues Romana Russian Shqip Slovensko Slovensky Srpski Suomi Svenska Thai Turkce Ukrainian Vietnamese Mode Guides Laurence-Moon Syndrome Web Sites Laurence Moon Bardet Biedl Society [Site Info] [Translate] [Open New Window] Fully accessible site for people with LMBB, their families, friends, carers and interested professionals. Opinions, news, views, research, updates, and contact details. URL: http://www.lmbbs.org.uk
Laurence-Moon Syndrome The New Health Directory, Directory, Home Health Conditions and Diseases Genetic Disorders laurencemoon syndrome (4) See Also http://www.thenewhealthfind.com/Health/ConditionsandDiseases/GeneticDisorders/La
Health - Conditions And Diseases - Genetic Disorders - Laurence Top Health Conditions and Diseases Genetic Disorders laurencemoon syndrome See also Health Conditions and Diseases Neurological http://www.sedirectory.net/Health/Conditions_and_Diseases/Genetic_Disorders/Laur
Extractions: Web Hosting Dir Web Design Dir Search Engine Dir Hardware Info ... Resources Search: 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. 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. Pediatric Database - A definition of Laurence-Moon syndrome followed by the epidemiology, pathogenesis, clinical features, investigations and management.
Laurence-Moon Bardet-Biedl Syndrome BardetBiedl syndrome is often confused with laurence-moon syndrome. laurence-moon syndrome is extremely rare; only a few case have been documented. http://www.blindness.org/laurence-moon-bardet-biedl-syndrome.asp
Extractions: Microsoft WebSpeak has been installed to read content on this site aloud. When you see this speaker icon, use your mouse to click on it and the wizard will be activated. Email Newsletter Sign up here for the latest research and science news, and FDA-approved clinical trials related to retinal degenerative diseases. Login Register Benefit Bardet-Biedl syndrome is often referred to as Laurence-Moon Bardet-Biedl syndrome or Laurence-Moon/Biedl syndrome. Bardet-Biedl syndrome is often confused with Laurence-Moon syndrome. Individuals with Laurence-Moon syndrome almost always experience neurologic problems but rarely polydactyly. Polydactyly is a defining feature of Bardet-Biedl syndrome, while neurologic problems almost never occur. Laurence-Moon syndrome is extremely rare; only a few case have been documented. Because of the similarity of these syndromes, Bardet-Biedl syndrome is often referred to as Laurence-Moon Bardet-Biedl syndrome or Laurence-Moon/Biedl syndrome.
Laurence-Moon Bardet-Biedel Syndrome BardetBiedel syndrome is often confused with laurence-moon syndrome. laurence-moon syndrome is extremely rare; only a few case have been documented. http://www.blindness.org/laurence-moon-bardet-biedel-syndrome.asp
Extractions: Microsoft WebSpeak has been installed to read content on this site aloud. When you see this speaker icon, use your mouse to click on it and the wizard will be activated. Email Newsletter Sign up here for the latest research and science news, and FDA-approved clinical trials related to retinal degenerative diseases. Login Register Benefit Bardet-Biedel syndrome is often referred to as Laurence-Moon Bardet-Biedel syndrome (correctly spelled Laurence-Moon Bardet Biedl ) or Laurence-Moon/Biedel syndrome. Bardet-Biedel syndrome is often confused with Laurence-Moon syndrome. Individuals with Laurence-Moon syndrome almost always experience neurologic problems but rarely polydactyly. Polydactyly is a defining feature of Bardet-Biedel syndrome, while neurologic problems almost never occur. Laurence-Moon syndrome is extremely rare; only a few case have been documented. Because of the similarity of these syndromes, Bardet-Biedel syndrome is often referred to as Laurence-Moon Bardet-Biedel syndrome or Laurence-Moon/Biedel syndrome.
Penn State Faculty Research Expertise Database (FRED) Faculty Research Expertise Database. laurencemoon syndrome. Laurence Moon Syndrome, Syndrome, Laurence-Moon. Syndrome, Laurence-Moon-Biedl, Faculty Experts, http://fred.hmc.psu.edu/ds/retrieve/fred/meshdescriptor/D007849
Penn State Faculty Research Expertise Database (FRED) This syndrome has been distinguished as a separate entity from laurencemoon syndrome. Laurence Moon Bardet Biedl Syndrome, Syndrome, Bardet-Biedl. http://fred.hmc.psu.edu/ds/retrieve/fred/meshdescriptor/D020788
»»Reviews For Laurence-Moon Syndrome«« laurencemoon syndrome Reviews. Related Subjects Genetic_Disorders More Pages laurence-moon syndrome Page 1 2. Search site for a Book Review. http://www.booksunderreview.com/Health/Conditions_and_Diseases/Genetic_Disorders
Extractions: Buy one from zShops for: Average review score: Excellent Educational Text "...a detailed practical guide for management of patients with genetic conditions...an asset to the bookshelf of any healthcare provider...also an excellent educational text..." (Journal of Genetic Counseling, Vol. 12, No. 4, August 2003) Useful Book "...quite useful to anyone...interested in a taste of what emerging technologies in genomics, proteomics, and bioinformatics can bring to bear on questions of potential importance in biomedical research." (American Journal of Human Genetics, Vol. 72, 2003) "a wealth of practical information" Cassidy and Allanson have assembled a talented group of authors to address the more common genetic disorders. The chapters are extremely well organized and each emphasizes not only diagnostic techniques and differential diagnosis, but also patient management. The generalist will find a wealth of practical information readily available and accessible. The clinical geneticist will discover and rediscover valuable "pearls" within this text. Edward R.B. McCabe, Department of Pediatrics, Mattel Children's Hospital at UCLA Hereditary Hearing Loss and Its Syndromes (Oxford Monographs on Medical Genetics, No 28)
Extractions: Front Page Today's Digest Week in Review Email Updates ... Genetic Disorders Laurence-Moon Syndrome (4 links) See Also: News about Laurence-Moon Syndrome New Cardiac Arrhythmia Syndrome Identified (June 1, 2004) full story Silence Of The Genes: Researchers Provide Unique View Of Inherited Disorders And Cancer (June 1, 2004) full story NASA Plans For Proposed Jupiter Mission (May 31, 2004) full story Scientists Discover Undersea Volcano Off Antarctica (May 31, 2004) full story Scientists Look At Moon To Shed Light On Earth's Climate (May 28, 2004)
