41. Mental Diseases laurencemoon syndrome. (LM Syndrome , Laurence Syndrome , Adipogenital-RetinitisPigmentosa Syndrome ). laurence-moon syndrome http://www.thirdaid.com/index/qfm/fuseaction/registrationStep3/catalog_id/10521/

42. LMBB Society | Research phenotype with the laurencemoon syndrome and propose a unifying, description ever produced of Laurence-Moon-Bardet-Biedl Syndrome in the medical http://www.lmbbs.org.uk/research.htm

LMBBS Laurence Moon Bardet Biedl Society Registered Charity Number 1027384 Research The Society co-operates with genetic research projects with the aim of mapping the LMBBS genes and learning more about the complex nature of the Syndrome. The rare nature of the Syndrome makes co-ordination of such a project difficult which is why the work of the Society is so valuable. Latest Research The latest article to appear in a medical journal was written by Dr Philip Beales in conjuction with others including our very own Drina Parker. It is detailed below and a pdf version of the paper can be found at the Journal Of Medical Genetics (J Med Genet 1999;36:437-446) New criteria for improved diagnosis of Bardet-Biedl syndrome: results of a population survey by P L Beales, N Elcioglu, A S Woolf, D Parker, F A Flinter (J Med Genet 1999;36:437-446) Abstract (J Med Genet 1999;36:437-446) Keywords: Bardet-Biedl syndrome; diagnosis; renal malformation; heterozygotes More than Meets the Eye Thanks largely to members of the Society completing a comprehensive questionnaire, Dr Philip Beales' 1997 survey on LMBB Syndrome proved to be the most significant survey on the Syndrome that has ever been conducted. Surveys such as this are important to all concerned in building up accurate knowledge of the Syndrome, particularly for the medical profession and carers. Following Dr Beales' successful survey, last July we published the most comprehensive description ever produced of Laurence-Moon-Bardet-Biedl Syndrome in the medical booklet

43. New Criteria For Improved Diagnosis Of Bardet-Biedl Syndrome: Results Of A Popul The overlap between BardetBiedl syndrome and laurence-moon syndrome has been Klein D, Ammann F. The syndrome of Laurence-Moon-Bardet-Biedl and allied http://jmg.bmjjournals.com/cgi/content/full/36/6/437

HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS Author Keyword(s) Vol Page [Advanced] This Article Abstract Full Text (PDF) Submit a response ... Citation Map Services Email this link to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Cited by other online articles PubMed PubMed Citation Articles by Beales, P L Articles by Flinter, F A Related Collections Genetics J Med Genet 437-446 ( June ) New criteria for improved diagnosis of Bardet-Biedl syndrome: results of a population survey P L Beales a N Elcioglu b A S Woolf c D Parker d F A Flinter a a Department of Medical and Molecular Genetics, 8th Floor Guy's Tower, Guy's Hospital, London SE1 9RT, UK, b Genetics Department, Cerrahpasa Medical School, Istanbul, Turkey, c Nephrourology Unit, Institute of Child Health, University College London Medical School, London WC1N 1EH, UK, d Laurence-Moon-Bardet-Biedl Society, Spring Grove, Loudhams Wood Lane, Chalfont St Giles, Bucks HP8 4AR, UK

44. EMedicine - Glucocorticoid Therapy And Cushing Syndrome : Article By George P Ch laurencemoon syndrome (MIM 245800) Bardet-Biedl syndrome, 6 types (chromosomearms 2q31; 3p13-p12; 11q13; 15q22.3-q23; 16q21; 20p12) http://www.emedicine.com/ped/topic1068.htm

(advertisement) Home Specialties Resource Centers CME ... Patient Education Articles Images CME Advanced Search Consumer Health Link to this site Back to: eMedicine Specialties Pediatrics Endocrinology Glucocorticoid Therapy and Cushing Syndrome Last Updated: December 6, 2002 Rate this Article Email to a Colleague Synonyms and related keywords: Cushing's syndrome, CS, Cushing disease, Cushing's disease, CD, hypercortisolism AUTHOR INFORMATION Section 1 of 11 Author Information Introduction Clinical Differentials ... Bibliography Author: George P Chrousos, MD, FAAP, MACP, MACE , Chief, Pediatric Endocrinology Section, NICHD/NIH; Clinical Professor, Departments of Pediatrics, Physiology, and Biophysics, Georgetown University Medical School Coauthor(s): Antony Lafferty, MB ChB, FRACP , Senior Lecturer of Pediatric Endocrinology, Monash University Department of Pediatrics, National Institutes of Health, Bethesda, MD, and Princess Margaret Hospital for Children, Perth, Western Australia George P Chrousos, MD, FAAP, MACP, MACE, is a member of the following medical societies: Association of American Physicians

45. APA Books laurencemoon syndrome David S. Nathanson. 53. Lead Exposure LeAdelle Phelpsand David S. Nathanson. 54. Lesch-Nyhan Disease http://www.apa.org/books/4312060t.html

APA Members/ Affiliates: List: $39.95 Item # 4312060 ISBN: Health-Related Disorders in Children and Adolescents : A Guidebook for Understanding and Educating: Contents "Editor: LeAdelle Phelps" May 1998 Hardcover 743 Pages Table of Contents List of Contributors Acknowledgments Part I: Background Information 1. How to Use This Book LeAdelle Phelps 2. A Guide to Genetics LeAdelle Phelps 3. Role of the School-Based Professional in Health-Related Services Thomas J. Power, George J. DuPaul, Edward S. Shapiro, and John M. Parrish Part II: Health-Related Disorders 4. Achondroplasia (Dwarfism) Georgia Frey and Douglas Palmer 5. Adrenoleukodystrophy Harvey N. Switzky, James P. Van Haneghan, and Abigail Baxter 6. Albinism Frank Murtha 7. Angelman Syndrome Richard J. Morris and Yuonne P. Morris 8. Apert Syndrome (Acrocephalosyndactyly Type I) Georgia Frey and Douglas Palmer 9. Arthritis (Juvenile Rheumatoid) Eric L. Robinson 10. Asperger's Disorder

46. APA Books This volume covers many poorly understood disorders (like laurencemoon syndromeand Rett syndrome), as well as more commonly occurring ones (like ear http://www.apa.org/books/4312060.html

APA Members/ Affiliates: List: $39.95 Item # 4312060 ISBN: Health-Related Disorders in Children and Adolescents : A Guidebook for Understanding and Educating "Editor: LeAdelle Phelps" May 1998 Hardcover 743 Pages SALE WAS: $49.95 members; $59.95 list NOW: $34.95 members; $39.95 list National and state law now mandate that school professionals provide education and care for children with health and handicapping disorders. Health-Related Disorders in Children and Adolescents contains succinct, up-to-date reviews of 96 medical conditions that describe the educational, psychological, and behavioral challenges that those involved in the care of children must respond to. This volume covers many poorly understood disorders (like Laurence-Moon syndrome and Rett syndrome), as well as more commonly occurring ones (like ear infections, cerebral palsy, and sickle-cell anemia). This volume is a resource for practitioners and medical professionals. Each chapter reviews the etiology of the disorder, which is followed by a section on the expected behavioral and physical outcomes. Next, authors describe psychoeducational implications and cover interventions that school psychologists, school-based professionals, and medical professionals can use to help ease the suffering of these children. The practical value of each chapter is enhanced by inclusion of an annotated bibliography, a list of resources for support organizations and informa-tion centers, and clear definitions for complex medical terminology. School personnel will also find this an invaluable resource and useful bibliographic tool to help educate parents on the problems their chlldren are facing.

47. Link Directory - Finnish Information Center On Mental Retardation Laurence Moon Bardet Biedl Syndrome, Genetics Education Center University ofKansas Medical Center Net Health_Conditions laurence-moon syndrome http://www.saunalahti.fi/kup/engl/webs_l.html

Finnish Information Center on Mental Retardation English links A B C D ... Z Lambotte syndrome Lambotte syndrome, OMIM, Victor A. McKusick Private multiple congenital anomaly syndromes may result from unbalanced subtle translocations: t(2q;4p) explains the Lambotte syndrome., Herens C et al, PubMed Lambotte syndrome: microcephaly, holoprosencephaly, intrauterine growth retardation, facial anomalies, and early lethalitya new sublethal multiple congenital anomaly/mental retardation syndrome in four sibs, Verloes A et. al, PubMed Langer-Giedion Syndrome Langer-Giedion Syndrome; LGS, OMIM, Victor A. McKusick Trichorhinophalangeal Syndrome Type II (NORD) Langer Giedion Syndrome Home Page, The University of Houston Langer Giedion Syndrome Association, USA ... Yahoo! Directory Langer-Giedion Syndrome Laurence-Moon-Bardet-Biedl Syndrome Laurence-Moon-Bardet-Biedl Syndrome, Family Village LAURENCE-MOON SYNDROME, OMIM, Victor A. McKusick BARDET-BIEDL SYNDROME; BBS, OMIM, Victor A. McKusick et al. BBS1 GENE; BBS1, OMIM. Victor A. McKusick ... The Laurence-Moon-Bardet-Biedl Society Lennox-Gastaut Syndrome Lennox-Gastaut Syndrome, EPINET, Epilepsy Foundation of Victoria (Australia)

48. DeCS - Changed Terms KINKY HAIR SYNDROME, MENKES KINKY HAIR SYNDROME. LAURENCEMOON-BIEDL SYNDROME,laurence-moon syndrome. MAXIMUM PERMISSIBLE EXPOSURE LEVEL, MAXIMUM ALLOWABLE http://decs.bvs.br/I/rep_i2000.htm

DeCS 2000 - Changed terms Replaced Replaced-by ACOUSTIC NERVE VESTIBULOCOCHLEAR NERVE ACOUSTIC NERVE DISEASES VESTIBULOCOCHLEAR NERVE DISEASES ADIE'S SYNDROME ADIE SYNDROME AMYGDALOID BODY AMYGDALA ANDROGEN-BINDING PROTEINS ANDROGEN-BINDING PROTEIN ANOSMIA OLFACTION DISORDERS APRAXIA APRAXIAS ARNOLD-CHIARI DEFORMITY ARNOLD-CHIARI MALFORMATION ASPARTIC PROTEINASES ASPARTIC ENDOPEPTIDASES CALLUS BONY CALLUS CEREBELLAR DYSSYNERGIA MYOCLONIC CEREBELLAR DYSSYNERGIA CEREBRAL ANEURYSM INTRACRANIAL ANEURYSM CEREBRAL ANOXIA HYPOXIA, BRAIN CEREBRAL ARTERIOSCLEROSIS INTRACRANIAL ARTERIOSCLEROSIS CEREBRAL ARTERIOVENOUS MALFORMATIONS INTRACRANIAL ARTERIOVENOUS MALFORMATIONS CEREBRAL ARTERY DISEASES CEREBRAL ARTERIAL DISEASES CEREBRAL EMBOLISM AND THROMBOSIS INTRACRANIAL EMBOLISM AND THROMBOSIS CEREBRAL ISCHEMIA BRAIN ISCHEMIA CEREBRAL ISCHEMIA, TRANSIENT ISCHEMIC ATTACK, TRANSIENT CEREBRAL SCLEROSIS, DIFFUSE DIFFUSE CEREBRAL SCLEROSIS OF SCHILDER CEREBROSPINAL OTORRHEA CEREBROSPINAL FLUID OTORRHEA CEREBROSPINAL RHINORRHEA CEREBROSPINAL FLUID RHINORRHEA CHARCOT-MARIE DISEASE CHARCOT-MARIE-TOOTH DISEASE CHORDATA CHORDATA, NONVERTEBRATE

49. OMIM - LAURENCE-MOON SYNDROME http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=245800

50. Entrez PubMed Hypogonadism laurencemoon syndrome/diagnosis laurence-moon syndrome/genetics*Male Mental Retardation/epidemiology Obesity/epidemiology Phenotype* http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=4

51. The IFOND Dictionary - L, International Foundation For Optic Nerve Disease laurencemoon syndrome A syndrome of mental retardation, pigmentary retinopathy,hypogenitalism, and spastic paraplegia. see OMIM 245800 http://www.ifond.org/dict_l.php3

I nternational F oundation for O ptic N erve D isease P. O. Box 777, Cornwall NY 12518, USA Providing and disseminating information on causes, prevention and treatment. Feedback HOME Page: A B C D ... Index The IFOND Dictionary - L L-Type Calcium channel Lamina Cribrosa Layer of connective tissue continuous with the sclera through which the retinal ganglion cell axons pass in the anterior part of the optic nerve. This area roughly coincides with the point where the retinal ganglion cell axons aquire their myelin sheaths and with abrupt changes in mitochondrial numbers. As a result of this unique anatomy, theories of retinal ganglion cell death often revolve around this disc. A. Bristow, P.G Griffiths, R.M. Andrews, M.A. Johnson, D. Turnbull. The relationship of mitochondrial activity to structure and function of the optic nerve. ARVO 2000 conference, Program Nr: 675. Lateral Geniculate Nucleus Major terminus of retinal ganglion cell axons. A nucleus of synapses in the thalamus. Divides into 6 layers with intercalated zones. There are four superficial parvocellular layers and two deeper magnocellular layers. The midget cell axons from the macula terminate in the parvocellullar area. The more peripheral parasol cell axons terminate in the magnocellular zones. Laurence-Moon syndrome A syndrome of mental retardation, pigmentary retinopathy, hypogenitalism, and spastic paraplegia. see

52. Rare Pediatric Disease Database and was formerly grouped with laurencemoon syndrome as the Laurence-Moon-Biedldisease. Bardet-Biedl syndrome is now considered as a separate entity. http://www.madisonsfoundation.org/content/3/1/display.asp?did=263

53. MT Desk: Word Lists - Neonatal Terms LactAid STARTrainer Nursing System™; Langer-Giedion syndrome; lanugo; large forgestational age (LGA); Larsen syndrome; laurence-moon syndrome http://www.mtdesk.com/lists_neonatal.shtml

Neonatal Terms Click here to return to the list of word lists. ABO incompatibility ABO hemolytic disease of the newborn ACPS (acrocephalopolysyndactyly) acne neonatorum acrocephaly acrocephalic acrocephalosyndactyly acrocephalopolysyndactyly (ACPS) adiponecrosis subcutanea neonatorum adjusted gestational age AENNS (Albert Einstein Neonatal Developmental Scale) AFP (alpha-fetoprotein) AGA (appropriate for gestational age) AIHA (autoimmune hemolytic anemia) alar flaring Albert Einstein Neonatal Developmental Scale (AENNS) alobar holoprosencephaly alpha-1 antitrypsin deficiency alpha-fetoprotein (AFP) aminophylline amnionic band syndrome ampicillin and gentamicin ("amp&gent") anencephaly aneuploidy aniridia Apgar score APIB (Assessment of Preterm Infant’s Behavior) apnea neonatorum apnea of prematurity appropriate for gestational age (AGA) Apt test arachnodactyly arrhinencephaly Arnold-Chiari deformity Arnold-Chiari malformation Arnold-Chiari syndrome ASD (atrioventricular septal defect) ASD (atrioseptal defect) atrioseptal defect (ASD) atrioventricular septal defect (ASD) autosome Babinski reflex BABYbird II respirator BABYbird II ventilator Babyflex ventilator BAER test (brain stem auditory-evoked response) bag-and-mask ventilation Bair Hugger® warmer blanket - Augustine Medical, Inc.

54. Arquivos Brasileiros De Oftalmologia - Translate this page Bell J. The laurence-moon syndrome. In Penrose LS, ed. Laurence-Moon-Biedlsyndrome, associated with multiple genitourinary tract anomalies. Am J Dis. http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-27492003000500024

55. UNSW Embryo- Select Pituitary Entries From OMIM *245800 laurencemoon syndrome *269700 BERARDINELLI-SEIP CONGENITAL LIPODYSTROPHY;BSCL *176760 PROLACTIN; PRL *602663 PROLACTIN-RELEASING HORMONE http://embryology.med.unsw.edu.au/OMIMfind/endocrine/pitlist.htm

UNSW Embryology DEVELOPMENT OF THE ENDOCRINE SYSTEM- Pituitary Embryology Home Page Page Links: Pituitary About Notes Other Pages: Pituitary Development Endocrine Development Endocrine Histology OMIM Endocrine Selected ... search OMIM Introduction Below are entries from a search of the Online Mendelian Inheritance in Man database. Clicking on the entry number will show the complete entry (see sample Heading List ) and links to other databases (see Database List top of page Pituitary 219 entries found, searching for "pituitary" POU DOMAIN, CLASS 1, TRANSCRIPTION FACTOR 1; POU1F1 PAIRED-LIKE HOMEODOMAIN TRANSCRIPTION FACTOR 1; PITX1 PITUITARY DWARFISM IV PROPHET OF PIT1, PAIRED-LIKE HOMEODOMAIN TRANSCRIPTION FACTOR; PROP1 GROWTH HORMONE 1; GH1 HYPERTHYROIDISM, FAMILIAL, DUE TO INAPPROPRIATE THYROTROPIN SECRETION PAIRED-LIKE HOMEODOMAIN TRANSCRIPTION FACTOR 2; PITX2

56. La : On Medical Dictionary Online Laurence Moon Biedl Syndrome Laurence Moon Syndrome laurencemoon syndrome Laurence-Moon-Bardet-Biedl Syndrome Laurence-Moon-Biedl Syndrome http://www.online-medical-dictionary.org/la.asp?q=~La

57. NCCS - Search NTEE Definitions JervellLange Nielsen Syndrome; Kartagener Syndrome; Klinefelter Syndrome;laurence-moon syndrome; Leigh Disease; Lesch-Nyhan Syndrome; Littles Disease; http://nccsdataweb.urban.org/PubApps/nteeSearch.php?gQry=G25

58. Search By Disease laurencemoon syndrome. 41, LC Collagen. 42, LCA, LCA1, CORD6, GUC2D, retGC,GUC1A4, RETGC-1, ROS-GC1. 43, LCA2, RP20. 44, LCA2, RP20. 45, LCA4, AIPL2 http://www.eddnal.com/directory/disease.php?letter=L&page=3

59. Assessment Of Abnormal Growth Curves - July 1998 - American Academy Of Family Ph Genetic disorders Down syndrome PraderWilli syndrome laurence-moon syndrome Ligament laxity and skin hyperelasticity suggest Marfan syndrome. http://www.aafp.org/afp/980700ap/legler.html

Advanced Search AAFP Home Page Journals Vol. 58/No. 1 (July, 1998) ... Patient Information Assessment of Abnormal Growth Curves JAMES D. LEGLER, M.D., and LEWIS C. ROSE, M.D. University of Texas Health Science Center at San Antonio, San Antonio, Texas An important part of well-child care is the assessment of a child's growth. While growth in the vast majority of children falls within normal percentile ranges on standard growth curves, an occasional child demonstrates worrisome deviations in weight, height or head size. A single growth percentile value at any particular point in a child's life is only of limited usefulness to the physician. More important is the child's rate of growth. Children whose growth parameters are at the extremes of the growth curve but whose growth rates are normal are likely to be healthy. Conversely, accelerated or slowed growth rates are rarely normal and warrant further evaluation. This article addresses the initial steps to be taken when evaluating children with suspected growth abnormalities, the guiding principles that apply to all growth problems, and the most common growth curve deviations and approaches to their management. W hile growth in nearly all children falls within normal percentile ranges on standard growth curves, an occasional child deviates in weight, height or head size. Before addressing these common growth curve deviations, the physician must consider the following four principles of growth assessment to determine if an abnormality is present.

60. Bardet-Biedl Syndrome - Wikipedia, The Free Encyclopedia LaurenceMoon-Biedl syndrome and Laurence-Moon-Biedl-Bardet syndrome are no longer laurence-moon syndrome is a separate entity. Major Features http://en.wikipedia.org/wiki/Bardet-Biedl_syndrome

You did it! Over US$240,000 was donated in the 21 day fund drive. Thank you for your generosity! You are still welcome to make a donation or purchase Wikimedia merchandise Bardet-Biedl syndrome From Wikipedia, the free encyclopedia. Laurence-Moon-Biedl syndrome and Laurence-Moon-Biedl-Bardet redirect here. See below for an explanation. The Bardet-Biedl syndrome is a a syndrome characterized mainly by obesity , pigmentary retinopathy polydactyly mental retardation hypogonadism , and renal failure in fatal cases. The syndrome is named after Georges Bardet and Arthur Biedl 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. edit Major Features: Eyes: Pigmentary retinopathy.

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