LMBBS Home Page laurencemoon syndrome (LMS) is characterised by retinitis pigmentosa (more accurately termed rod-cone dystrophy), mental retardation, hypogenitalism and http://www.isgrd.umds.ac.uk/laurence/
Extractions: Laurence-Moon-Bardet-Biedl Syndrome (LMBBS) 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. CONTENTS HISTORY rod-cone dystrophy ), mental retardation, hypogenitalism and spastic paraparesis. Bardet-Biedl syndrome (BBS) has as the main features RP (rod-cone dystrophy), obesity, postaxial polydactyly, learning disabilities and hypogenitalism (males). This latter subgroup represents by far the majority of published cases and is now the preferred term amongst the medical and scientific community. As there are many cases of overlap between the LMS and BBS we shall for the purposes of this publication make no distinction and therefore refer to LMBBS throughout. John Zachariah Laurence c.1870
NORD - National Organization For Rare Disorders, Inc. General Discussion. laurencemoon syndrome is a rare inherited disorder characterized by literature regarding the difference between laurence-moon syndrome and Bardet-Biedl Syndrome http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Laurence Moon
Laurence-Moon Syndrome Information Diseases Database laurencemoon syndrome, Disease Database Information Sponsors Contact Previous Page. laurence-moon syndrome Information. laurence-moon syndrome Definition(s) via UMLS ..Code translations and terms via UMLS http://www.diseasesdatabase.com/ddb30072.htm
Laurence Moon Bardet Biedl Syndrome Lauurence Moon Bardet Biedl Syndrome Resources, international support groups, clinics, genetic counselors and geneticists Hospital London. laurencemoon syndrome, Pediatric Database (PEDBASE) Laurence-Moon http://www.kumc.edu/gec/support/laurmoon.html
Laurence-Moon Syndrome Multiple Congenital Anomaly/Mental Retardation (MCA/MR) Syndromes. View the Full Record. Syndrome. laurencemoon syndrome. Summary. A syndrome of mental retardation, retinitis pigmentosa, hypogonadism, and spastic paraplegia. and spastic paraplegia. Laurence-Moon-Biedl syndrome and Laurence-Moon-Biedl-Bardet syndrome are no http://www.nlm.nih.gov/mesh/jablonski/syndromes/syndrome393.html
Extractions: Syndrome Laurence-Moon syndrome Summary A syndrome of mental retardation, retinitis pigmentosa, hypogonadism, and spastic paraplegia. Laurence-Moon-Biedl syndrome and Laurence-Moon-Biedl-Bardet syndrome are no longer considered as valid terms in that patients with Laurence and Moon had spastic paraplegia but no polydactyly and obesity which were the key elements in the Bardet and Biedl patients. Bardet-Biedl syndrome is a separate entity. Major Features Eyes: Pigmentary retinopathy. Nervous system: Spastic paraplegia. Urogenital system: Hypogonadism. Growth and development: Mental retardation. Heredity: The syndrome is familial and is transmitted as an autosomal recessive trait.
NORD - National Organization For Rare Disorders, Inc. Confusion exists in the medical literature regarding the difference between BardetBiedl Syndrome and laurence-moon syndrome. . http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Bardet Biedl
Pediatric Database A definition of laurencemoon syndrome followed by the epidemiology, pathogenesis, clinical features, investigations and management. http://www.icondata.com/health/pedbase/files/LAURENCE.HTM
Extractions: Web Directory: 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.
Laurence Moon Syndrome Laurence Moon Syndrome. Confusion exists in the medical literature regarding the difference between laurencemoon syndrome and Bardet-Biedl Syndrome. http://www.bchealthguide.org/kbase/nord/nord104.htm
Extractions: It is possible that the main title of the report 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. Information on the following diseases can be found in the Related Disorders section of this report: 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."
Bardet Biedl Syndrome Confusion exists in the medical literature regarding the difference between BardetBiedl Syndrome and laurence-moon syndrome. . Symptoms. http://www.bchealthguide.org/kbase/nord/nord988.htm
Extractions: It is possible that the main title of the report 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. Information on the following diseases can be found in the Related Disorders section of 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. The Bardet-Biedl Syndromes are also frequently characterized by abnormalities of the numbers of fingers and/or toes (digits) as well as obesity that is often limited to the trunk. Digital abnormalities may include extra fingers and/or toes (polydactyly), webbing of certain digits (syndactyly) (characteristically the second and third toes), and/or abnormal shortness of the digits (brachydactyly) compared to the palm length. In addition, the feet tend to be unusually short, broad, and flat, with no arch.
WebMD Health - 404 Error More results from my.webmd.com OMIM laurence-moon syndrome http://my.webmd.com/content/healthwise/82/20340
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Bardet-Biedl Syndrome (BBS) markers on chromosome 16. LaurenceMoon-Biedl syndrome and Laurence-Moon-Biedl-Bardet syndrome are no the Bardet-Biedl the syndrome. laurence-moon syndrome is a separate entity http://www.nlm.nih.gov/mesh/jablonski/syndromes/syndrome048.html
Extractions: 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.
OMIM - %245800 LAURENCE-MOON SYNDROME %245800 laurencemoon syndrome. TEXT. The laurence-moon syndrome (strictu sensu) is the same as the disorder reported by Kapuscinski (1934). http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?cmd=entry&id=245800
Extractions: Ablepharon-Macrostomia Syndrome ... Genetic Disorders : Laurence-Moon Syndrome Bardet-Biedl Syndrome, Laurence-Moon/Bardet-Biedl,Biedl-Bardet ... - Confusion exists in the medical literature regarding the difference between Bardet-Biedl Syndrome and Laurence-Moon Syndrome. Some Conditions and Diseases: Genetic Disorders: Laurence-Moon Syndrome ... - Conditions and Diseases: Genetic Disorders: Laurence-Moon Syndrome. See also: Health: Conditions and Diseases: Neurological Disorders: Brain Diseases (117); Genetic Disorders / Laurence-Moon Syndrome - Genetic Disorders / Laurence-Moon Syndrome. Categories related to Laurence-Moon Syndrome: Geometry.Net - Health_Conditions: Laurence-moon Syndrome - Pediatric Database (PEDBASE). Discipline: GEN; Last Updated: 12/23/94 LAURENCE-MOON SYNDROME. DEFINITION: Laurence-Moon syndrome. Direct access to details Alias : Health Information Resource Database: Laurence-Moon-Biedl Syndrome ... - Laurence-Moon-Biedl Syndrome Network. Contact Information. Sonya Coster 124 Lincoln Ave Purchase, NY 10577. 914-251-1163 (Voice). Internet Resources. Health Library - Laurence Moon Syndrome - Laurence Moon Syndrome. Confusion exists in the medical literature regarding the difference between Laurence-Moon Syndrome and Bardet-Biedl Syndrome.
Conditions And Diseases - Laurence-Moon Syndrome Top Links laurencemoon syndrome Web Site Links. NORD - Laurence Moon Syndrome - Offers alternative names, a general discussion and further resources. http://www.disease-resources.com/Top_Health_Conditions_and_Diseases_Genetic_Diso
Extractions: Related Healthcare Subjects Disabilities Environmental Health Fitness Health Insurance ... Men's Health Laurence-Moon Syndrome Web Site Links 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.
Genetic Disorders, Laurence-Moon Syndrome Submit Your Site to the laurencemoon syndrome category. Sponsored laurence-moon syndrome Sites. Submit Your Site to the laurence-moon syndrome category. http://www.iseekhealth.com/laurence-moon_syndrome-1595.php
Extractions: 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.
Genetic Disorders, Laurence-Moon Syndrome Category Home Health Conditions and Diseases Genetic Disorders laurencemoon syndrome. * Site Title · The name of the site. http://www.iseekhealth.com/directory/index.php?method=show_link_exchange&directo
Extractions: 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." Find more information on the Internet with
