61. Laurence-Moon-Biedl Syndrome » Medical Diagnosis And Advice Medical Diagnosis Advice » L » LaurenceMoon-Biedl syndrome MISCELLANEOUS.SYNONYMS. • laurence-moon syndrome • Bardet-Biedl syndrome http://www.htmdesigner.com/diag/L/medical-diagnosis-terms-Laurence_Moon_Biedl_sy

Medical Diagnosis and Advice Search A B ... Z Laurence-Moon-Biedl syndrome Laurence-Moon-Biedl syndrome OVERVIEW: A hereditary syndrome of childhood, transmitted as an autosomal recessive trait, with obesity, retinitis pigmentosa, mental retardation, polydactyly, and hypogonadism as the main features. Usual course - progressive. CAUSES: TREATMENT MISCELLANEOUS SYNONYMS: ICD-9-CM: 759.8 Laurence-Moon-Biedl syndrome see images Want to discuss this term? Visit our forum or our chat room SEE ALSO (Enter the keywords below into our search box or click on the link): n/a Web medfamily.org Total Medical Terms: Rate this site! 1 - Worst 10 - Best Joint Partnership with Med School Chat part of the School Chat Network By viewing this website, you agree to our We're still here, you rockin' with the best! Best View with 1024x768 screen and IE 5.0 Although the HTM Designer materials have been developed by physicians and health care provider it is designed for educational purposes only. The site is not engaged in rendering medical advice. The information provided should not be used for diagnosing or treating a health problem or a disease. It is not a substitute for professional care. It is solely for information and second opinion purposes. If you have or suspect you may have a health problem, you should consult your health care provider and use the information here as a cross references. The authors, editors, producers, sponsors, and contributors shall have no liability, obligation or responsibility to any person or entity for any loss, damage, or adverse consequence alleged to have happened directly or indirectly as a consequence of this material.

62. 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 helpful? 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.

63. Bardet-Biedl Syndrome Topic - Unified Search Environment MTH/MM/U009322 MTH/MM/U009323 MSH/PM/D020788 MTH/PT/125 laurencemoon-Bardet-BiedlSyndrome MSH/EP/D020788 MSH/PM/D020788 MSH/PM/D020788 http://www.use.hcn.com.au/portals/shared/subject.`Bardet-Biedl Syndrome`/home.ht

Bardet-Biedl Syndrome Topic Tree Definition: 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) Synonyms and Source Vocabularies: Bardet-Biedl Syndrome Laurence-Moon-Bardet-Biedl Syndrome Congenital Abnormality Abnormalities, Drug-Induced Abnormalities, Multiple Basal Cell Nevus Syndrome Beckwith-Wiedemann Syndrome Bloom Syndrome Cockayne Syndrome ... Congenital neurologic anomalies

64. Laurence-Moon-Biedl Syndrome - Patient UK laurencemoon-Biedl syndrome - Patient UK. A directory of UK health, disease,illness and related medical websites that provide patient information. http://www.patient.co.uk/showdoc/40001405/

PatientPlus articles are written for doctors and so the language can be technical. However, some people find that they add depth to the articles found in the other sections of this website which are written for non-medical people. Laurence-Moon Syndrome Previously known as: Laurence Moon Biedel Syndrome, Laurence-Moon Bardet-Biedl syndrome This genetic autosomal recessive disorder presents in childhood and is characterised by progressive neurological, ophthalmic and endocrine manifestations which deteriorate to cause eventual blindness and spastic paraplegia Presentation Hypogenitalism is present at birth (hypogonadotrophic hypogonadism noted postpubertally). Retinitis pigmentosa night blindness and progressive visual loss), mental retardation and ataxia become apparent during childhood. The progressive spastic paraplegia results in a bedridden state by early adulthood. Management There is no treatment for underlying condition. A multidisciplinary approach is required involving paediatrics, neurology, ophthalmology, endocrinology and genetic counselling This syndrome is distinct from the Bardet-Biedl syndrome because of the presence of paraplegia; and absence

65. Laurence Moon (Bardet Biedl) Syndrome (LMBBS) Laurence Moon (Bardet Biedl) syndrome (LMBBS). BardetBiedl laurence-moon Syndroom laurence-moon-Bardet-Biedl syndrome syndrome de http://www.bdid.com/lmbbs.htm

HOME Laurence Moon (Bardet Biedl) Syndrome (LMBBS) Bardet-Biedl Laurence-Moon Syndroom Laurence-Moon-Bardet-Biedl Syndrome Syndrome de Laurence-Moon-Bardet-Biedl Laurence-Moon-Bardet-Biedl Network ... Laurence-Moon-Bardet-Biedl Syndrome Also see Bardet Biedl Syndrome HOME

66. Penn State Faculty Research Expertise Database (FRED) laurencemoon-Bardet-Biedl syndrome, Bardet Biedl syndrome. Laurence Moon BardetBiedl syndrome, syndrome, Bardet-Biedl. syndrome, laurence-moon-Bardet- http://fred.hmc.psu.edu/ds/retrieve/fred/meshdescriptor/D020788

67. Laurence-Moon, Syndrome : Sites Et Documents Francophones Translate this page laurence-moon, syndrome de Par Dr Aymé S (Orphanet - INSERM SC 11). Site éditeurOrphanet base de données sur les maladies rares et les médicaments http://www.chu-rouen.fr/ssf/pathol/laurencemoonsyndrome.html

Laurence-Moon, syndrome Synonyme(s) CISMeF Laurence-Moon. Voir aussi retard mental Ne pas confondre avec syndrome de Bardet-Biedl Arborescence(s) Laurence-Moon, syndrome Laurence Moon syndrome maladies du système nerveux maladies et malformations congénitales, héréditaires et néonatales Position du mot-clé dans l' (les) arborescence(s) : Vous pouvez consulter toutes les ressources ou seulement les principales ou utiliser l' outil de recherche les recommandations les documents concernant l' enseignement les documents destinés aux patients Ou consulter ci-dessous une sélection des principales ressources : patient Laurence-Moon, syndrome de [Par Dr Aymé S (Orphanet - INSERM SC 11). Site éditeur Orphanet base de données sur les maladies rares et les médicaments orphelins. Direction Générale de la Santé / INSERM ; signes de la maladie, sites internet, dysmorphologie, conseil génétique, associations de patients ; pays : France ; langue : français ; format : html ; accès : gratuit ; non parrainé ; daté de : 2002 ; visité le : 17/09/2003]. mots clés : conseil génétique *Laurence-Moon, syndrome

68. Laurence-moon, Syndrome : Arborescences MeSH http://www.chu-rouen.fr/navimesh/L/navilaurencemoonsyndrome.html

Laurence-moon, syndrome : arborescences MeSH Vous pouvez aussi consulter toutes les arborescences des mots clés utilisés dans CISMeF maladies du système nerveux maladie du système nerveux central encéphalopathies hypothalamus, maladies ... Wolfram, syndrome 25 février 2005 courriel Menu général CISMeF Haut de page © CHU de Rouen . Toute utilisation partielle ou totale de ce document doit mentionner la source.

69. 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 Laurence Moon Syndrome from OMIM Bardet-Biedl Syndrome, Type II About Laurence-Moon Bardet-Biedl Syndrome Web Sites Laurence-Moon-Bardet-Biedl Syndrome Page Laurence-Moon-Bardet-Biedl Network Home Page 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

70. Bardet-Biedl Syndrome laurencemoon-Bardet-Biedl syndrome; Bardet Biedl syndrome; Laurence Moon BardetBiedl syndrome; syndrome, Bardet-Biedl; syndrome, laurence-moon-Bardet- http://medical.webends.com/kw/Bardet-Biedl Syndrome

Medical.WebEnds.com - Medical Terminology Dictionary A B C D ... Z WWW Medical.WebEnds.com Bardet-Biedl Syndrome Laurence-Moon-Bardet-Biedl Syndrome; Bardet Biedl Syndrome; Laurence Moon Bardet Biedl Syndrome; Syndrome, Bardet-Biedl; Syndrome, Laurence-Moon-Bardet-Biedl 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) Google links Processing time was 0.042476892471313 seconds.

71. Laurence-Moon-Bardet-Biedl Syndrome - Healthfinder® The information on this page is provided for medical and healthcare professionalsinvolved in the care of LMBBS patients and also for parents or relatives http://mentalhealth.about.com/library/h/docs/bld04497.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-Bardet-Biedl Syndrome internet URL http://www.isgrd.umds.ac.uk/laurence/ sponsoring agency Commercial EntityFollow the Resource URL for More Information description The information on this page is provided for 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. Keywords: Consumer Resources Genetics Laurence-Moon-Biedl Syndrome Patient Education 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

72. Bardet-Biedl Syndrome - Laurence-Moon-Bardet-Biedl Syndrome - Information Page W An autosomal recessive disorder characterized by RETINITIS PIGMENTOSA; POLYDACTY http://www.hon.ch/HONselect/RareDiseases/EN/C10.228.140.617.200.html

InitBulle("navy","#F8F8F8","#000066",1); HONcode sites All Web sites HONselect News ... Images HONselect Search English French German Spanish Portuguese the word the part of word in MeSH term in MeSH term and description Information on "Bardet-Biedl Syndrome": Medical hierarchy and definition Research Articles Web resources Medical Images Medical News Medical Conferences Clinical Trials Hierarchy English French German Spanish Portuguese Bardet-Biedl Syndrome Definition: 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) Synonym(s): Laurence-Moon-Bardet-Biedl Syndrome / Bardet Biedl Syndrome / Laurence Moon Bardet Biedl Syndrome / Syndrome, Bardet-Biedl / See also: Mental Retardation See Related: Obesity Polydactyly Laurence-Moon Syndrome Retinitis Pigmentosa ... New search Web resources for "Bardet-Biedl Syndrome" English French German Spanish = Site with HON description - = Site with a robot description info: enter the site: (click below) domain of the site: http://www.blindness.org/visiondisorders/causes.asp?type=27

73. Laurence-Moon, Syndrome De Translate this page Base de données sur les maladies rares et les médicaments orphelins. http://www.orpha.net/static/FR/laurencemoon.html

Accès à la base de données Orphanet Laurence-Moon, syndrome de Accès direct aux détails Résumé Le syndrome de Laurence-Moon est un syndrome génétique autosomique récessif d'étiologie inconnue. Il est caractérisé par des manifestations neurologiques, ophtalmologiques et endocriniennes progressives provoquant une détérioration gravement handicapante. Les manifestions neurologiques incluent un retard mental et une ataxie qui conduit à une paraplégie spastique progressive chez l'adulte jeune. Les manifestations ophtalmologiques consistent en des taches rétiniennes dues à la finesse de la rétine ; celles-ci évoluent vers une atrophie optique entraînant une cécité. Un hypogénitalisme est présent dès la naissance. Il est lié à un hypogonadisme hypogonadotrope. La prise en charge tend à palier les déficits. Ce syndrome est plus fréquent dans la population arabe du Koweït. *Auteur : Equipe Editoriale d'Orphanet (septembre 2002)*. Signes de la maladie ANTITRAGUS ANORMAL OBESITE GENERALISEE POLYDACTYLIE DU MEMBRE SUPERIEUR RETARD MENTAL / PSYCHO-MOTEUR SYNDACTYLIE DES DOIGTS TRANSMISSION AUTOSOMIQUE RECESSIVE INSUFFISANCE RENALE MICROPENIS/VERGE PETITE PETITE TAILLE / NANISME SURDITE DE PERCEPTION TESTICULE ECTOPIE/CRYPTORCHIDIE ATAXIE / INCOORDINATION BRACHYCEPHALIE/OCCIPUT PLAT CARDIOPATHIE CONGENITALE CATARACTE DIPLEGIE/PARAPLEGIE/QUADRIPLEGIE EPICANTHUS FIBROSE HEPATIQUE CONGENITALE HYPERGLYCEMIE/DIABETE NON INS. DEP.

74. Special Child: Disorder Zone Archives - Laurence-Moon-Bardet-Biedl Syndrome laurencemoon-Bardet-Biedl syndrome (LMBBS) is an autosomal recessive genetic Recently, however, the syndrome was split into laurence-moon (LMS) and http://www.specialchild.com/archives/dz-035.html

Disorder Zone Archives Laurence-Moon-Bardet-Biedl Syndrome Sabrina Parker Introduction Laurence-Moon-Bardet-Biedl syndrome (LMBBS) is an autosomal recessive genetic disorder characterized by obesity, retinal degeneration, extra digits on the hands and feet, and intellectual impairment. In an autosomal recessive disorder, both parents must be carriers of the defective gene and both must pass on the defect to the child in order for the child to be affected. If both parents carry the defective gene responsible for causing LMBBS, they have a 1 in 4 chance of having a child with the syndrome. In 1993, the gene responsible for LMBBS was located on chromosome 16q21 (type 2). Shortly thereafter, another gene on chromosome 11q13 (type 1) was identified. Since then, two others were found on chromosomes 3p12 (type 3) and 15q22 (type 4). The most common form of LMBBS is type 1 and the most rare form is type 3. It is expected, however, that another gene that causes the syndrome also exists because there are identified cases that have none of these four defects. The occurrence rate varies in different parts of the world. In regions such as Kuwait, the occurrence is 1 in 13,500 due to a high frequency of inter-family marriages. British studies, on the other hand, show the prevalence to be 1 in 160,000. While this syndrome is considered rare, it is suspected that there is a major problem with under-diagnosis. Features and Characteristics Following is a list of characteristics that have been seen in children with LMBBS. Not all children will exhibit all of these features:

75. Bardet-Biedl And Cohen Syndromes: Differential Diagnostic Criteria -- WARBURG Et The spectrum of renal disease in laurencemoon-Biedl syndrome. N Engl J Med1988;319615-618Abstract. 9. Schachat AP, Maumenee IH. Bardet-Biedl syndrome http://jmg.bmjjournals.com/cgi/content/full/37/12/e46

HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS Author Keyword(s) Vol Page [Advanced] This Article Extract Full Text (PDF) Submit a response ... Alert me if a correction is posted Services Email this link to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Download to citation manager PubMed PubMed Citation Articles by WARBURG, M. Articles by FLINTER, F. Related Collections Genetics J Med Genet e46 ( December ) Electronic letters Bardet-Biedl and Cohen syndromes: differential diagnostic criteria Reply to letter Bardet-Biedl and Cohen syndromes: differential diagnostic criteria E DITOR Fig 1 in the paper by Beales et al shows portraits of six patients with the Bardet-Biedl syndrome (BBS). Number 4, the lower left picture, has the facial appearance of the Cohen syndrome (CS) with apparent microcephaly, thick hair, coarse eyebrows, short philtrum, and prominent incisors. Since she is presented

76. Syndrome Of Bardet-Biedl laurencemoon-Biedl-Bardet s syndrome, can not be considered as such since inBardet-Biedl s syndrome does not exist paraplegia (paralysis) and in http://www.obesidad.net/english2002/disorder9.shtml

Bardet-Biedl's syndrome Health has no price Obesidad.net is educational Visit us continually. You will always find new advice for your health. Recommend this site. Recommend this site to a friend or relative who may find it helpful BARDET-BIEDL'S SYNDROME Bardet-Biedl's syndrome is a hereditary disease that affects many parts of the body. Obesity, the pygmentary retinitis (night blindness and the progressive loss of the peripheral vision), the mental delay, the hypogonadism, the renal damage and the polydactylia (fingers extra in the feet), define the characteristics of Bardet-Biedl's syndrome. INHERITANCE Two forms have been identified: Bardet-Biedl's syndrome 1, which does not have relation with the chromosome 16. Bardet-Biedl's syndrome 2, that has relation with the chromosome 16. Bardet-Biedl's syndrome is transmitted genetically across the families by inheritance autosomic recessive. In this type of inheritance, both parents are called carriers, they have a gene of the syndrome paired with a normal gene. Each of his children have at the time a possibility of 25% (or an opportunity in four) of inheriting both Bardet-Biedl's genes (one of every father) necessary to cause this disease. The carriers are healthy because only they have a copy of the gene. At this moment, it is impossible to determine if someone is a carrier of Bardet-Biedl's syndrome but until the birth of an affected child.

77. Online And Offline Support: L People served Families dealing with Laurence Moon Bardet Biedl syndrome;Services provided laurencemoon-Biedl syndrome Network (United States) http://www.widesmiles.org/support/l.html

L Langer-Giedion Syndrome Langer-Giedion Syndrome Association People served: Individuals and families dealing with Langer-Giedion Syndrome Services provided: Information, public awareness, support for families, newsletter, and advocacy for research Contact people: Raquel Rozenberg Address: 9021 45th Ave. N, Minneapolis MN 55428 Email address: roze0002@umn.edu Louise Kinross 89 Ingham Ave. Toronto, Ont. M4K 2W8, Canada Email address: kinross@istar.ca Email address: lgsa@geocities.com Website: http://www.geocities.com/HotSprings/9308/ Laurence-Moon-Bardet-Biedl Syndrome Please note: Laurence-Moon-Bardet-Biedl Syndrome includes specific facial characteristics that do not require reconstructive surgery. The LMBBS Society (United Kingdom) People served: Families dealing with Laurence-Moon-Biedl Syndrome Services provided: Support and information Address: Spring Grove, Loudhams Wood Lane, Chalfont St Giles Bucks HP8 4AR Phone number: 01494 764924 Laurence Moon Bardet Biedl Syndrome (United States) People served: Families dealing with Laurence Moon Bardet Biedl Syndrome Services provided: Support and information Address: 124 Lincoln Avenue, Purchase NY 10577

78. Laurence-Moon-Bardet-Biedl Syndrome Network Home Page The purpose of this page is to raise public awareness of the LaurenceMoonBardet-Biedl syndrome. It will also serve as a place for parents of LMBBS http://mlmorris.com/lmbbs/

Welcome to the Laurence-Moon-Bardet-Biedl Network Home Page The purpose of this page is to raise public awareness of the Laurence-Moon Bardet-Biedl syndrome. It will also serve as a place for parents of LMBBS children to meet and exchange ideas. View our gift shop! Purchase your LMBBS merchandise here! CLICK HERE Next Page This Blindness and Visual Impairment site owned by Mary Morris Previous 5 Sites Skip Previous Previous ... List Sites This page hosted by

79. Search Result For "Laurence-Moon-Bardet- Biedl Syndrome(LMBBS)" NOAH pages containing laurencemoon-Bardet- Biedl syndrome(LMBBS) . Displaying 1-5of 338. Retinitis Pigmentosa The Eye Clinic and Retinitis Pigmentosa; http://www.noah-health.org/search/results.php?lang=1&keyword=Laurence-Moon-Barde

80. HEALTHMEDNET Laurence Moon syndrome. laurencemoon. laurence-moon-Bardet-Biedl syndrome.laurence-moon-Biedl syndrome. Lavage. Laxative. Laxatives For Constipation http://www.epscorp.com/healthmednet/l.htm

Directory Index HEALTHMEDNET Example Report Request ... DataBase Note: The names were derived from the specific illness/disease source directories. Therefore, there are some variations in the names. When ordering a list of URLs for your illness/disease, where possible, include the general usage, technical, acronym, and/or abbreviation names. Laband Syndrome Labia Majora Labia Minora Labial Labial frenulum Labium Labor Labor and Delivery Labor Pain, False Laboratory Infection Labyrinth Labyrinth Diseases Labyrinth Disorders Labyrinthine Hydrops Labyrinthitis (Vestibular Disorders) Laceration Lack of intrinsic factor Lacrimal Apparatus Diseases Lacrimal Duct Obstruction Lacrimal Glands Lacrimation Lactase Deficiency (Lactose Intolerance) Lactation Lactation Disorders Lactation Problems Lactic Acid Lactic-Acidosis Lactose Lactose Intolerance Lacunar stroke LADD Syndrome Laetrile Lamaze Lambert-Eaton Myasthenic Syndrome Lambliosis (Giardia lamblia) Lamellar ichthyosis Lameness Laminectomy LAMM (Heroin Treatment) Lamotrigine [for Epilepsy] Lance Landau Kleffner Syndrome Langer-Giedion Syndrome Langerhans' Islands Langerhans-Cell Granulomatosis Language Disorders Lanolin Lanugo Laparoscopic Anti-Reflux Surgery Laparoscopic gallbladder surgery for gallstones Laparoscopic hernia repair [for Inguinal Hernia] Laparoscopic lymphadenectomy [in Prostate Cancer] Laparoscopic Sterilization Laparoscopic Surgery Laparoscopic surgery for endometriosis Laparoscopic surgery for functional ovarian cysts Laparoscopy Laparoscopy for functional ovarian cysts Laparoscopy for uterine fibroids

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