81. Alström's Syndrome (www.whonamedit.com) Alström s syndrome A syndrome similar to (laurencemoon-)Biedl-Bardet thatmanifests with obesity in childhood, nerve deafness and retinal degeneration http://www.whonamedit.com/synd.cfm/511.html

Home List categories Eponyms A-Z Biographies by country ... Contact Whonamedit.com does not give medical advice. This survey of medical eponyms and the persons behind them is meant as a general interest site only. No information found here must under any circumstances be used for medical purposes, diagnostically, therapeutically or otherwise. If you, or anybody close to you, is affected, or believe to be affected, by any condition mentioned here: see a doctor. A recommendation: Hypography is an open community about science and all things related Alström's syndrome Also known as: Alström-Hallgren syndrome Hallgren-Alström syndrome Synonyms: Retino-otodiabetic syndrome. Associated persons: Carl-Henry Alström Bertil Hallgren Description: A syndrome similar to (Laurence-Moon-)Biedl-Bardet that manifests with obesity in childhood, nerve deafness and retinal degeneration (atypical retinitis pigmentosa). Blindness usually occurs by age 7 years. Primary hypogonadism in males, and juvenile diabetes mellitus. Acanthosis nigricans, hypogonadism with normal secondary sex characteristics, and kyphoscoliosis may be associated. Metabolic findings include hyperuricaemia and elevated serum triglycerides and pre-ß-lipoproteins. Mental capacity is normal. Inheritance is autosomal recessive. Only 104 children and adults (by 2001) world-wide are known to have this extremely rare condition. Most cases are in developed countries such as Canada, the United States of America and the United Kingdom, the latter having the largest group of diagnosed patients.

82. Health Library - laurencemoon-Biedl syndrome » Medical Diagnosislaurence-moon-Biedl syndrome. MISCELLANEOUS. SYNONYMS. • laurence-moonsyndrome • Bardet-Biedl syndrome. ICD-9-CM. 759.8 laurence-moon-Biedl syndrome http://12.31.13.113/library/healthguide/en-us/illnessconditions/topic.asp?hwid=n

83. Healthfinder® - Laurence-Moon-Biedl Syndrome Carefully selected government and nonprofit health information on laurencemoon-BiedlSyndrome. http://www.healthfinder.gov/Scripts/SearchContext.asp?topic=485

84. Laurence Moon Syndrome Laurence Moon syndrome is a rare inherited disorder characterized by diminishedhormone production by http://my.webmd.com/hw/raising_a_family/nord104.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 Laurence Moon Syndrome Important It is possible that the main title of the report Laurence Moon 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 Adipogenital-Retinitis Pigmentosa Syndrome Laurence Syndrome LM Syndrome Disorder Subdivisions None General Discussion 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). Confusion exists in the medical literature regarding the difference between Laurence-Moon Syndrome and Bardet-Biedl Syndrome. Some researchers believe that Bardet-Biedl Syndrome is a subdivision of Laurence-Moon Syndrome which they term "Laurence-Moon-Biedl Syndrome." Resources National Association for Visually Handicapped 22 West 21st Street New York, NY 10010

85. NORD - National Organization For Rare Disorders, Inc. Laurence Moon Bardet Biedl syndrome. 11435 Cronhill Drive Owings Mills MD 211172220Phone 410-568-0150 800 888-394-3937 e-mail info@blindness.org http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Bardet Biedl

86. Hill Health Topics A-Z - Laurence Moon Syndrome Laurence Moon syndrome. National Organization for Rare Disorders. Important Itis possible that the main title of the report Laurence Moon syndrome is not http://www.healthwise.net/hillhealth/Content/StdDocument.aspx?DOCHWID=nord104&SE

87. RedNova News - Science - Laurence Moon Syndrome RedNova Health LinkLaurence Moon SyndromeSynonyms AdipogenitalRetinitis PigmentosaSyndromeLaurence SyndromeLM SyndromeMore science, space, http://www.rednova.com/news/science/3062/laurence_moon_syndrome/

ANDP("ntn"); Ads_kid=0;Ads_bid=0;Ads_xl=0;Ads_yl=0;Ads_xp='';Ads_yp='';Ads_xp1='';Ads_yp1='';Ads_opt=0;Ads_wrd='[KeyWord]';Ads_prf='';Ads_par='';Ads_cnturl='';Ads_sec=0;Ads_channels=''; Home News Video Images ... Site Map SPECIAL NEWS Return to Flight REDNOVA NEWS Space Science Technology Health ... Video News REDNOVA EXTRAS RedNova E-Mail My RedNova Join RedNova RSS Feeds ... Tell A Friend, Win $500 Ads by Google Posted on: Wednesday, 1 January 2003, 06:00 CST E-mail this to a friend Printable version Discuss this story in the forum Change Font Size: A A A Laurence Moon Syndrome RedNova Health Link Laurence Moon Syndrome Synonyms: Adipogenital-Retinitis Pigmentosa Syndrome Laurence Syndrome LM Syndrome More science, space, and technology from RedNova Ads by Google More News in this Category E-mail this to a friend Printable version Discuss this story in the forum a d v e r t i s e m e n t QUIZ ME Should the citizens who refuse leave hurricane affected areas be forced to leave? Yes No View results RedNova.com RedNova Advertising About Us Contact Us Privacy Statement ... Abuse Reporting Ads_kid=0;Ads_bid=0;Ads_xl=728;Ads_yl=90;Ads_xp='';Ads_yp='';Ads_opt=0;Ads_wrd='';Ads_prf='';Ads_par='';Ads_cnturl='';Ads_sec=0;Ads_channels='728X90-ALL'; showAd("news_stories_728x90_top"); showAd("news_articles_d1"); showAd("news_articles_d2"); //showAd("google_wide");

88. Laurence Moon Bardet Biedl Syndrome Lauurence Moon Bardet Biedl syndrome Resources, international support groups,clinics, genetic counselors and geneticists. http://www.kumc.edu/gec/support/laurmoon.html

Laurence Moon Bardet Biedl Syndrome Laurence Moon Bardet Biedl Syndrome Network Laurence-Moon-Bardet-Biedl Syndrome , Canada Laurence-Moon-Bardet-Biedl Syndrome (LMBBS) , Molecular and Medical Genetics, Prince Philip Research Laboratories, Guy's Hospital London Laurence-Moon-Bardet-Biedl Society , United Kingdom Bardet-Biedl Laurence-Moon Syndrome , Belgium or Dutch LMBBS discussion group,(Laurence Moon Baardet-Beidl Syndrome) , Australia Syndrome de Laurence-Moon-Bardet-Biedl France Laurence-Moon Syndrome , Online Mendelian Inheritance in Man (OMIM) #245800 Bardet-Biedl Syndrome (BBS) , Online Mendelian Inheritance in Man (OMIM) Laurence Moon , signs of condition, Orphanet Laurence-Moon-Bardet-Biedl Syndrome , WideSmiles Also See: National organizations information on genetic conditions or birth defects Information for siblings and family members , genetic conditions Vision Impairment / Blindness Resources To locate a genetic counselor or clinical geneticist in your area: Professional Genetics Societies Genetic clinics, centers, departments

89. Laurence Moon Syndrome Synonyms, Eastern Carolina Laurence Moon syndrome Synonyms University Health Systems of Eastern Carolinaserves tarboro, ahoskie, edento, winsor, maxhead, dear county, http://www.uhseast.com/113312.cfm

Health News Health Library Health Topics Healthy Living ... Nutrition Information on diseases and health concerns, including symptoms, treatment options, and prevention. Laurence Moon Syndrome Synonyms Disorder Subdivisions General Discussion Resources ... For a Complete Report Important It is possible that the main title of the report Laurence Moon 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 Adipogenital-Retinitis Pigmentosa Syndrome Laurence Syndrome LM Syndrome Disorder Subdivisions None General Discussion 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). Confusion exists in the medical literature regarding the difference between Laurence-Moon Syndrome and Bardet-Biedl Syndrome. Some researchers believe that Bardet-Biedl Syndrome is a subdivision of Laurence-Moon Syndrome which they term "Laurence-Moon-Biedl Syndrome." Resources National Association for Visually Handicapped 22 West 21st Street New York, NY 10010

90. Congenital, Hereditary, And Neonatal Diseases And Abnormalities An laurencemoon-Bardet-Biedl Society - (UK). About laurence-moon-Bardet-BiedlSyndrome - Guy s Hospital, London (UK) http://www.mic.ki.se/Diseases/c16.html

search search staff sitemap ABOUT KAROLINSKA INSTITUTET ... print this page Diseases and Disorders Links pertaining to Congenital, Hereditary, and Neonatal Diseases and Abnormalities Alert! Patients and laypersons looking for guidance among the target sources of this collection of links are strongly advised to review the information retrieved with their professional health care provider. Start Page Contents: Abnormalities Aicardi Syndrome (not on MeSH) Amniotic Band Syndrome Anencephaly ... Wolf-Hirschhorn Syndrome (not on MeSH) Congenital, Hereditary, and Neonatal Diseases and Abnormalities The US National Organization for Rare Disorders , including a Rare Disease Database , and a List of Disease-specific Organizations Search Jablonski's MCA/MR Syndromes Database -NOTE: info may be outdated!! [Congenital Abnormalities associated with Mental Retardation] - NLM (US) Indice delle malattie [in Italian] - InformaGene (IT) A Short History of Mapping [B Mertz] - Access Excellence GENATLAS: Pathology Search [J Frezal] - Univ Rene Descartes, Paris (FR) OrphaNet [rare diseases] - (FR) A Birth Disorder Information Directory - Spamgid.com

91. Laurence Moon Syndrome - Healthfinder® Basic consumer information about Laurence Moon syndrome including a list ofsynonyms and resources where you can get additional information. http://mentalhealth.about.com/library/h/docs/bld04526.htm

zJs=10 zJs=11 zJs=12 zJs=13 zc(5,'jsc',zJs,9999999,'') zfs=0;zCMt='a14' About Mental Health Resources Mental Health Essentials ... Help zau(256,140,140,'el','http://z.about.com/0/ip/417/C.htm','');w(xb+xb+' ');zau(256,140,140,'von','http://z.about.com/0/ip/496/6.htm','');w(xb+xb); FREE Newsletter Sign Up Now for the Mental Health Resources newsletter! See Online Courses Search Mental Health Resources Laurence Moon Syndrome internet URL sponsoring agency National Organization for Rare Disorders, Inc. description Basic consumer information about Laurence Moon Syndrome including a list of synonyms and resources where you can get additional information. Keywords: Birth Defect Children Consumer Resources Laurence-Moon-Biedl Syndrome Mental Retardation Rare Diseases Retinitis Pigmentosa From Leonard Holmes, Ph.D. Your Guide to Mental Health Resources FREE Newsletter. Sign Up Now! zau(256,420,100,'ri','http://z.about.com/5/o/c.htm?gs='+gs,'') Most Popular Video Bathroom Decoration Ideas Tag Sale Tips Creating a Craft Room Making a Personal Space ... See other videos at About.com Advertisement Most Popular MAO Inhibitors Cymbalta gets Mixed Reviews Video Game Violence Psychiatric Medications - Introduction, Antipsychotics

92. Syndrome De Bardet-Biedl - Syndrome De Laurence Moon Bardet Biedl HONsélect Translate this page syndrome de Bardet-Biedl - articles, sites web, images, http://www.hon.ch/HONselect/RareDiseases/FR/C10.228.140.617.200.html

InitBulle("navy","#F8F8F8","#000066",1); sites HONcode sites Web HONsélect News ... Images Chercher HONsélect Anglais Français Allemand Espagnol Portugais le mot la partie du mot dans les termes MeSH Information pour "Syndrome de Bardet-Biedl": Hiérarchie médicale et definition Articles médicaux Ressources du Web Images médicales Nouvelles médicales Conférences médicales Hiérarchie Anglais Français Allemand Espagnol Portugais Syndrome de Bardet-Biedl Définition: An autosomal recessive disorder characterized by RETINITIS PIGMENTOSA POLYDACTYLY OBESITY MENTAL RETARDATION ; hypogenitalism; renal dysplasia; and short stature. This syndrome has been distinguished as a separate entity from LAURENCE-MOON SYNDROME . (From J Med Genet 1997 Feb;34(2):92-8) Synonyme(s): Syndrome de Laurence Moon Bardet Biedl / Voir également: Retard mental Voir connexe: Obésité Polydactylie Laurence-Moon, syndrome Rétinite pigmentaire (NLM)® de l'INSERM (version française) Parcourir Chercher HONsélect Ressources du Web pour "Syndrome de Bardet-Biedl" Anglais Français Allemand Espagnol = Site with HON description - = Site with a robot description info: entrez dans le site: (cliquez ci-dessous) domaine du site: www.retina-france.asso.fr

93. References For Bardet-Biedl Syndrome 2 With The MeSH Term syndrome. References for BardetBiedl syndrome 2 with the MeSH term Laurence-Moonsyndrome, G2D Home. PMID and date. Follow the link to see the http://www.bork.embl-heidelberg.de/g2d/exam_mesh_disease.pl?Laurence-Moon_Syndro

94. Eye Conditions BardetBiedl syndrome (Laurence Moon), FEVR, Peter s Anomaly BilateralRetinoblastoma, Laurence Moon syndrome (Bardet-Biedl), Rubella Infection http://www.spedex.com/napvi/eye_conditions.htm

National Association for Parents of Children with Visual Impairments (NAPVI) Eye Conditions Below is list of all the eye conditions and/or children's visual impairments currently in our database. NAPVI can refer members to other members whose children have similar impairments, so they can share their valuable experiences and information regarding these often very rare cases. Achromatopsia Congenital Toxoplasmosis Ocular Albinism Albinism Cortical Blindness Ocular Motor Apraxia Alopecia Cortical Visual Impairment Oculocutaneous Albinism (OCA) Alstrom's Disease De Morsier's Syndrome One-and-a-Half Syndrome Amblyopia Deaf/Blind Optic Atrophy Aniridia Deformed Optic Nerves Optic Glioma Anophthalmia Degenerative Retinal Disease Optic Nerve Aplasia Anorhomia deLange Syndrome (CdLS) Optic Nerve Damage Anterior Segment Dysgenesis Detached Retina Optic Nerve Glioma Aphakia Duane Syndrome Optic Nerve Hypoplasia Astrocytoma Dubowitz Syndrome Myopia Physiologic Ectodermal Dysplasia Persistent Hyperplastic Primary Vitreous Bardet-Biedl Syndrome (Laurence Moon) FEVR Peter's Anomaly Batten's Disease Filicubris Premature Retinopathy Bilateral Anophthalmia Foreal Hypoplasia Orbital Chordoma Bilateral Cataracts Fundus Flavimaculatus Rieger's Anomaly Bilateral Coloboma Glaucoma Retinal Disease Bilateral Ectopia Lentis Hallermann-Streiff Syndrome Retinal Disorder Hermansky-Pudlak Syndrome Retinal Dysplasia Bilateral Micro Ophthalmia Hydrocephalus Retinal Folds Bilateral Optic Nerve Aplasia Hyperopia Retinitis Pigmentosa Bilateral Optic Nerve Hypoplasia

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

96. Laurence-Moon-Bardet-Biedlin Oireyhtymä - Kehitysvamm. Tietopankki Research Laboratories, Guy s Hospital, London Laurence Moon Bardet BiedlSyndrome, Genetics Education Center University of Kansas Medical Center http://www.saunalahti.fi/kup/syndroma/lmbbs.htm

Kehitysvammahuollon tietopankki Lihavuus, epämuodostumia sekä CP- ja kehitysvammaisuus Laurence-Moon-Bardet-Biedlin oireyhtymä Laurence-Moonin syndrooma LMBBS Laurence-Moon-Bardet-Biedlin oireyhtymän tunnusmerkkejä ovat liikalihavuus, psyykkinen kehitysvammaisuus , kehittymättömät sukuelimet ja silmien verkkokalvojen rappeutuminen ( Retinitis Pigmentosa ). Myös munuaisten vauriot ja raajojen jäykkyys ( spastinen paraplegia ) sekä lisävarvas kuuluvat taudinkuvaan. Sairaus on harvinainen ja periytyvä. Periytyminen tapahtuu usein 11. tai 16. kromosomin välityksellä. Jälkimmäisessä tapauksessa on ollut tapana puhua taudin 2. tyypistä. Kaikkiaan oireistoon liittyviä geenivirheitä on tavattu seuraavasti: 20p12, 16q21, 15q22.3-q23, 14q32.1, 11q13, 4q27, 3p13-p12 ja 2q31. LMBBS-sairauden kuvasi ensimmäisenä englantilainen lääkäri John Zachariah Laurence yhdessä amerikkalaisen kollegansa tri Moonin kanssa 1866. Laurence-Moonin oireyhtymä yhdistettiin myöhemmin 1900-luvun alkupuolella Bardet-Biedlin oireyhtymään , koska sairauksien piirteet näyttivät samoilta. Oireyhtymän väitetään olevan normaalia yleisempi Kuwaitin arabiväestön (beduiinit) keskuudessa.

97. Children Living With Inherited Laurence Moon syndrome. Leber Congenital Amaurosis. Leber Hereditary OpticNeuroretinopathy. Leber Optic Atrophy. LHON http://www.climb.org.uk/Disorders/Lima.htm

Search Our Site C hildren L iving with I nherited M eta b olic Diseases Metabolic Diseases 'L' The National Information and Advice Centre for Metabolic Diseases Disease Also Known as L2 Hydroxyglutaric Aciduria Lactase Deficiency Lactic Acidosis Lactose Intolerance - Congenital Lafora Body Disease Laurence Moon Syndrome Leber Congenital Amaurosis Leber Hereditary Optic Neuroretinopathy Leber Optic Atrophy LHON Lecithin Cholesterol Acyl Transferase Deficiency LCAT Fish-eye Disease Leigh Disease – Adult Leigh Disease – Classical Leigh Disease – Infantile Lennox-Gastaut Syndrome Leprechaunism Leptin Deficiency Leptin Receptor Defects Lesch-Nyhan Disease Leukocyte Adhesion Deficiency Syndrome Type II Leukodystrophy – General Leukotriene C4-Synthesis Deficiency Ligneous Conjunctivitis Limb Girdle Muscular Dystrophy Lipid Storage Disease - General Lipoamide Dehydrogenase Deficiency Lipodystrophy – General Lipodystrophy - Barraquer-Simons Disease Cephaolthoracic Lipodystrophy or Progressive Lipodystrophy Lipodystrophy - Berardinelli-Seip Syndrome Seip Syndrome or Gongenital Generalised Lipodystrophy Lipodystrophy - Centrifugal Form Lipodystrophy - Dunnigan Form Lipodystrophy - Kobberling Form Lipodystrophy - Lawrence Syndrome Acquired Generalised Lipodystrophy Lipodystrophy - Mandibuloacral Dysplasia

98. A Listing Of Disorders Larsen syndrome. Laurence Moon syndrome. Leber s Congenital Amaurosis. Leber s OpticAtrophy. Legg Calve Perthes Disease. Legionnaire s Disease http://medschool.umaryland.edu/BTBank/Family/Disorders_L.htm

Brain and Tissue Bank University of Maryland, Baltimore L Laband Syndrome Lactose Intolerance LADD Syndrome Landau Kleffner Syndrome Laron Dwarfism Larsen Syndrome Laurence Moon Syndrome Leber's Congenital Amaurosis Leber's Optic Atrophy Legg Calve Perthes Disease Legionnaire's Disease Leigh's Disease Leiner Disease Lennox Gastaut Syndrome Lenz Microphthalmia Syndrome LEOPARD Syndrome Leprechaunism Leri Pleonosteosis Lesch Nyhan Syndrome Leukodystrophy Leukodystrophy, Canavan's Leukodystrophy, Krabbe's Leukodystrophy, Metachromatic Leukodystrophy, Sudanophilic Leukoencephalopathy Lichen Planus Lichen Sclerosus Lipodystrophy Lissencephaly Locked In Syndrome Loken Senior Syndrome Long Chain Acyl CoA Dehydrogenase Deficiency (LCAD) Lowe's Syndrome Lupus Lyelles Syndrome Lymphadenopathy, Angioimmunoblastic with Dysproteinemia Lymphangioleiomyomatosis Lymphangioma, Cavernous Lymphedema, Hereditary Lymphocytic Infiltrate of Jessner Lynch Syndromes

99. NCCS - Search NTEE Definitions Kartagener syndrome Research; Klinefelter syndrome Research; LaurenceMoonsyndrome Research; Leigh Disease Research; Lesch-Nyhan syndrome Research; http://nccsdataweb.urban.org/PubApps/nteeSearch.php?gQry=H25

100. Health Library - BardetBiedl laurence-moon SyndroomEen Belgische site over het Bardet-Biedl laurence-moon Syndroom. http://12.42.224.150/library/healthguide/en-us/illnessconditions/topic.asp?hwid=

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