41. M Website Results :: Linkspider UK Sensitivity@ (26); multiple hamartoma syndrome@ (3); Multiple Myeloma@(17); Multiple Personality Disorder@ (107); Multiple Sclerosis http://www.linkspider.co.uk/Health/ConditionsandDiseases/M/

M Websites from Linkspider UK Keyword: M Linkspider UK Directory M Search for Directory Tree: Top Health Conditions and Diseases : M (0) Add URL Advertise Here! Personalize Amazon ... Myotonic Dystrophy

42. Access 10,000 + Universities And Colleges At Universities.com - (campus And Dist 4); MRKH@ (13); Mucopolysaccharidosis 3@ (4); Multiple Chemical Sensitivity@(26); multiple hamartoma syndrome@ (3); Multiple Myeloma http://www.studentbody.com/Directory/Health/Conditions_and_Diseases/M/

StudentBody.com Home Pick A Degree AA in General Studies BS in Business *Accounting *Administration *Information Systems *Management *Marketing *Project Management *E-Business (NEW!) Bachelor of Science in Nursing (For RN's Only) BS Info Technology *Database Management *Networks and Telecommunications *Programming and Operating Systems *Systems Analysis *Web Management GRADUATE DEGREES MA Ed/ Curriculum and Tech. MA Org. Mgmt. MBA *Accounting *Global Management *Technology Management MS Computer Information MS Nursing DOCTORAL DEGREES Doctor of Mgmt. in Org. Leadership Home My Account Distance Learning Financial Aid ... Conditions and Diseases : M A B C D ... L M N O P Q ... Mysasthenia Gravis Conditions and Diseases " search on: All the Web AltaVista Deja Google ... Yahoo Help build the largest human-edited directory on the web. Submit a Site Open Directory Project Become an Editor Mon Mar 31 02:22:36 EST 2003

43. The Indian Journal Of Radiology And Imaging - Archives:19990901 - Radiological Q leontiasis ossea. Coexisting conditions in LDD include Cowden's disease,which is also called multiple hamartoma syndrome. It is http://www.ijri.org/archives/19990901/radquiz01.htm

Radiological Quiz - Neuroradiology SUREKHA K, AK GUPTA, SANTHOSH JOSEPH, KESAVADAS C, NKK PRABHU Ind J Radiol Imag 1999; 9:1: 25-27 A fifty-seven-years old man was well until one year prior to admission to the hospital. He developed recurrent attacks of headache and vomiting with increased frequency of symptoms about one month prior to admission. He also complained of swaying to either side. Examination revealed bilateral papilledema. In addition he also had multiple subcutaneous lipomas and papules over the body. CT and MR were performed (Figs. 1, 2). Fig 1 A Fig 1 B Fig.1 (A,B): T1W axial MR (A) and T2 W coronal MR (B) of the brain Fig. 2 : CT of the brain RADIOLOGICAL DIAGNOSIS: Lhermitte-Duclos Disease (LDD) CT shows an ill-defined hypodense lesion of the right cerebellum with significant mass effect (Fig. 1). MR reveals a hypointense mass on the T1W images (Fig. 2A) and a laminated, striated or folial pattern of increased signal on the T2W images (Fig. 2B). The patient underwent decompression and partial resection of the lesion. On surgery, the cerebellum showed thickened folia. Pathological features demonstrated were suggestive of Lhermitte-Duclos disease (LDD). Dermatological consultation with biopsy of skin lesions was consistent with Cowden's disease.

44. Guidelines Of Care For Nevi. II. Nonmelanocytic Nevi, Hamartomas, Neoplasms, And Allen BS, Fitch MH, Smith JG Jr. multiple hamartoma syndrome. J AM ACADDERMATOL 1980;23038. Amaral AL, Nascimento AG, Goellner JR. http://www.aadassociation.org/Guidelines/nevi.html

Guidelines of Care for Nevi. II. Nonmelanocytic Nevi, Hamartomas, Neoplasms, and Potentially Malignant Lesions This report reflects the best data available at the time the report was prepared, but caution should be exercised in interpreting the data; the results of future studies may require alteration of the conclusions or recommendations set forth in this report. Reprint requests: American Academy of Dermatology, P.O. Box 4014, Schaumburg, IL 60168-4014. J AM ACAD DERMATOL 1995;32:104-8 Guidelines of care for nevi. II. Nonmelanocytic nevi, hamartomas, neoplasms, and potentially malignant lesions Committee on Guidelines of Care : Lynn A. Drake, MD, Chairman, Roger I. Ceilley, MD, Raymond L. Cornelison, MD, William L. Dobes, MD, William Dorner, MD, Robert W. Goltz, MD, Gloria F. Graham, MD, Charles W. Lewis, MD, David M. Pariser, MD, Stuart J. Salasche, MD, John W.. Skouge, MD, Maria L. Chanco Turner, MD, and Barbara J. Lowery, MPH Task Force on Nevi, Part II: Robert W. Goltz, MD, Chairman, David R. Barron, MD, Alvin H. Clair, MD, Kenneth G. Gross, MD, and Charles W. Lewis, MD I. Introduction

45. Vindex, De Vindplaats Van Het Nederlandse Web Disorders@ Morvan Disease@, Mouth Cancer@ Moyamoya Disease@ Mucopolysaccharidosis3@ Multiple Chemical Sensitivity@ multiple hamartoma syndrome@ Multiple Myeloma http://www.vindex.nl/dir/Health/Conditions_and_Diseases/M

hulp contact persoonlijke instellingen voeg uw site toe ... Opties: Samenvatting 1 url per domein Sites in nieuw venster Staat uw webpagina nog niet in Vindex? Meld deze dan nu aan! Url: Emailadres: Zoek in de webgids: Terug naar het overzicht Huidige rubriek Health Conditions and Diseases M Subrubrieken MAC@ MPS III@ MRKH@ Machado-Joseph Disease@ ... Myotonic Dystrophy@ Links In deze rubriek zijn geen links gevonden... Kies een subrubriek of een verwante rubriek. Submit a Site Open Directory Project Become an Editor Powered by IBM -server IDG.nl vang.net Vragen? Opmerkingen? Suggesties?

46. M Information Sites Cancer@; Moyamoya Disease@; Mucopolysaccharidosis 3@; Multiple ChemicalSensitivity@; multiple hamartoma syndrome@; Multiple Myeloma@; Multiple http://www.healthorgs.com/ConditionsandDiseases/M/

HEALTHorgs.com Search The Largest Human Reviewed Health Database on Internet (Not sure of spelling? Use first letters and * such as abc* or abcd* or abcde*) Match:.. All Any Format: Long Short Search Words: Search the Internet (Not sure of spelling? Use first letters and * such as abc* or abcd* or abcde*) Match:.. All Any Format: Long Short Search Words: Top Health Conditions and Diseases : M MAC MPS III MRKH Machado-Joseph Disease ... (on approved loans) The content of the SPYorg.com directory is based on the Open Directory and is enhanced using Spyorg.com technology. Privacy Statement Add Your Site to SPYorg.com ADVERTISEMENT:

47. Alphabetical Topic Index (AZ) Jump To A B C D E F G H I J K L M Hallucinations Hallux Limitus Hallux Limitus Hallux Rigidus Hallux Rigidus HalluxValgus Hallux Valgus Hamartoma Syndrome, multiple hamartoma syndrome http://www.uscuh.com/apps/Intermap/topiclist/SectionH.html

Alphabetical Topic Index (A-Z): Jump To: A B C D ... Hy H Ha Haemonchiasis Haemonchiasis Hair Loss Hair Loss in Men And Women Hairy Tongue Tongue, Hairy Halitosis Halitosis Hallermann's Syndrome Hallermann's Syndrome Hallervorden-Spatz Syndrome Hallervorden-Spatz Syndrome Hallucinations Hallucinations Hallux Limitus Hallux Limitus Hallux Rigidus Hallux Rigidus Hallux Valgus Hallux Valgus Hamartoma Syndrome, Multiple Hamartoma Syndrome, Multiple Hand Deformities, Acquired Hand Deformities, Acquired Hand Deformities, Congenital Hand Deformities, Congenital Hand Dermatoses Hand Dermatoses Hand, Foot and Mouth Disease Hand, Foot and Mouth Disease Hantavirus Infection Hantavirus Pulmonary Syndrome Hartnup Disease Hartnup Disease Hay Fever Hay Fever Back To Top ^ He Head and Neck Cancer Hypopharyngeal Cancer Salivary Gland Cancer Parathyroid Cancer Paranasal Sinus And Nasal Cavity Cancer ... Oral Cavity Cancer Head Injuries, Closed Head Injuries, Closed Head Injuries, Penetrating Head Injuries, Penetrating Headache Headache Headache: Tension Tension Headaches Headaches: Cluster Cluster Headaches Hearing Loss, Age-Associated)

48. Diseases Database Disease, Symptom, Sign, Etc Alphabetical Index : L Diseases Da plasma or serum) Lhermitte's sign Lhermitte's syndrome see Internuclear ophthalmoplegiaLhermitteDuclos disease see multiple hamartoma syndrome LHRH see http://www.diseasesdatabase.com/sieve/disease_index_l.asp

Diseases Database [Previous page] [Search] [Index] [Feedback] Diseases Database disease, symptom, sign, etc alphabetical index : L L-DOPA L-xylulose reductase deficiency see Hereditary pentosuria La Crosse virus see California encephalitis virus Lab abnormality (all) see Laboratory finding Labetalol Labhardt-Willi-Prader-Fanconi syndrome see Prader-Willi syndrome Laboratory finding Labour (normal) Labour dysfunction see Dystocia Labyrinthine fistula Labyrinthitis Lacidipine Lack of energy see Fatigue Lacrimal gland enlarged Lacrosse encephalitis see California encephalitis virus Lactase deficiency Lactate dehydrogenase Lactate dehydrogenase levels low (plasma or serum) ... Lactate dehydrogenase levels raised (plasma or serum) Lactate levels raised (plasma or serum) see Lactic acidosis Lacteal cyst see Galactocoele Lactic acidaemia see Lactic acidosis Lactic acidosis Lactitol Lactobacillus acidophilus ... Lactobacillus delbrueckii ss. bulgaricus Lactocele see Galactocoele Lactose intolerance see Lactase deficiency Lactosuria Lactulose Lacunar infarction see Lacunar stroke Lacunar stroke Lafora body disease Lamellar ichthyosis see Collodion baby syndrome Lamivudine Lamotrigine Lamoxactam see Moxalactam Landau-Kleffner syndrome Landouzy-Dejerine disease see Facio-scapulo-humeral muscular dystrophy Lange Nielsen syndrome Langer mesomelic dysplasia syndrome Langer-Giedion syndrome ... Langer-Saldino achondrogenesis Langerhan's cell histiocytosis see Histiocytosis X Lanreotide Lansoprazole Lanugo hair ... Laparotomy Large bowel cancer see Colorectal cancer Large bowel obstruction Large for dates

49. Syndromes In Breast Cancer oral papules). It is also called as multiple hamartoma syndrome. PTENis a tumour suppressor gene located on 10q23 chromosome. The http://www.au-kbc.org/research_areas/bio/projects/bcinfo/gen/synd.html

AU-KBC RESEARCH CENTRE Syndromes associated with breast cancer The incidence of syndrome associated with breast cancer is very low (less than 1%). The various syndromes associated with breast cancer are: Li-Fraumeni syndrome: A large number of sporadic cancers are due to mutation in p53 but when this occurs in germline cells, it results in Li-Fraumeni syndrome. It is characterized by premenopausal breast cancer in combination with childhood soft tissue tumours, brain tumors, leukemia, lymphoma, and adrenocortical carcinoma. The probability that these individuals will develop breast cancer is 60% overall. Germline mutations are mostly seen in the exon 7 of p53 gene. [OMIM] Germline mutations in another gene, hCHK2, have been implicated in the etiology of one classical and two variant Li-Fraumeni families A detailed account of p53 is discussed here Cowden syndrome: It is an autosomal dominant syndrome characterized by hamartomatous lesions in the breast, GI tract (polyps), CNS (Central Nervous System), skin and mucosa, eyes, thyroid, genitourinary tract and bones. Germline mutations in the PTEN gene is responsible for this syndrome. Diagnosis is established through identification of characteristic skin lesions (acral keratosis, facial trichilemmomas, and oral papules). It is also called as multiple hamartoma syndrome. PTEN is a tumour suppressor gene located on 10q23 chromosome. The gene product of PTEN is a phosphatase which plays an important role in regulating cell growth. Mutation in PTEN gene results in loss of protein function leading to uncontrolled cell proliferation and hamartomatous growths.

50. DINO - Language: Englisch - Health - Conditions And Diseases - M Translate this page Link verweist auf eine Haupt-Kategorie Multiple Chemical Sensitivity Dieser Linkverweist auf eine Haupt-Kategorie multiple hamartoma syndrome Dieser Link http://www.dino-online.de/dino_page_24b646b8cd0e55a69f5ef091dac92489.html

Suche Profi-Suche Katalog Video ... Produkte Suchen: Web-Seiten Video Audio Bilder Produkte Schon gewusst? Hier suchen Sie in 2 Milliarden Webseiten. Live-Suche: Was suchen andere Dino-Besucher? You are here: DINO Language Englisch Health ... Conditions and Diseases M M Sprache/Language Categories MAC Machado-Joseph Disease Macular Degeneration Mad Cow Disease Madelung's Disease Malaria Male Turner Syndrome Malignant Atrophic Papulosis Malnutrition Mannosidosis Marburg Marfan Syndrome Marie-Sainton Disease Marinesco-Sjogren Syndrome Mayer Rokitansky Kuster Hauser Syndrome McArdle's Disease Measles, German Measles, Red Meckel-Gruber Syndrome Megaloblastic Anemia Meige Syndrome Melanoma Melorheostosis Menengitis, Cryptococcal Meniere's Disease Meningitis Menkes' Syndrome Menstrual Problems Mental Retardation Meralgia Paresthetica Mesothelioma Metachromatic Leukodystrophy Microphthalmia Microsporidiosis Migraine Miller Fisher Syndrome Minimal Change Disease Mitchell Disease Mitral Valve Disease Mitral Valve Prolapse Syndrome Mobius Syndrome Moersch-Woltmann Syndrome Mood Disorders Morvan Disease Mouth Cancer Moyamoya Disease MPS III MRKH Mucopolysaccharidosis 3 Multiple Chemical Sensitivity Multiple Hamartoma Syndrome Multiple Myeloma Multiple Personality Disorder Multiple Sclerosis Multiple System Atrophy Mumps Murmurs Muscle Disorders Muscular Dystrophies Myalgic Encephalomyelitis Mycoplasmal Myelitis Myelodysplastic Syndromes Myelosyringosis Myocardial Diseases Myocardial Infarction Myopathies Myotonic Dystrophy

51. Irritation Fibroma may represent cases of familial fibromatosis, fibrotic papillary hyperplasia of thepalate, tuberous sclerosis, or multiple hamartoma syndrome (Cowden syndrome http://www.maxillofacialcenter.com/BondBook/softtissue/fibroma.html

Irritation (Traumatic) Fibroma Quick Summary Introduction References Photos ... Prognosis Irritation fibromas under dentures are flat and "leaf-shaped." Quick Review for Patients The irritation fibroma is a painless, localized, mass-producing proliferation of dense fibrous "scar" tissue which can result from a single traumatic episode or from repeated, less severe traumatic episodes; chronic inflammation or infection may also produce a fibroma. The lesion can become more than 3 cm. in size but is usually less than 1 cm. It occurs at all ages and in both genders and specialized forms occur under dentures, along denture edges and on inflamed gingiva. The fibroma is best treated by conservative surgical or laser removal, with a small chance of recurrence should the originating irritation persist. There is no risk of malignant transformation. Top of This Page Introduction Note: click on underlined words for more detail or photos. Irritation fibroma

52. THE LIGHTNING HYPERTEXT OF DISEASE. syndrome = Langer mesomelic dysplasia syndrome Hamartomatosis = Hamartosis Cowdensyndrome = multiple hamartoma syndrome Encephalotrigeminal angiomatosis http://www.pathinfo.com/cgi-bin/lh.cgi?tx=ballergerold

53. GeneCard For PTEN the predominant phenotype for cs is multiple hamartoma syndrome, in many organ systemsincluding the breast (70% of cs patients), thyroid (4060%), skin, cns http://bioinfo.cnio.es/cgi-bin/db/genecards/carddisp?PTEN

54. MUMS List Of Disorders - C Syndrome (7) * ; Cowden Syndrome (multiple hamartoma syndrome) (4)*; CranioFronto-Nasal Dysplasia (2); Craniodiaphyseal Dysplasia http://www.netnet.net/mums/mum_c.htm

Return to MUMS Home Page MUMS: List of Disorders C Number in parentheses indicates number of matches. indicates there is a support group which covers that diagnosis. C-PAP (14) CATCH 22 Syndrome(DiGeorge+Velo-Cardio-Facial+Conotruncal) (5) * CHARGE Syndrome (49) * CHARGE-VATER Syndrome (2) Calcium Deficiency (26) Campomelic Dysplasia Syndrome (11) * Camptodactyly (5) Canavan's Leukodystrophy (3) * www.canavan.org/ Cancer (135) * www.cancer.org and www.candlelighters.org Cancer, Acute Lymphatic Leukemia (ALL) (6)* Cancer, Anoplastic Oligodendroglioma Tumor (1) Cancer, Chordoma (Spinal Tumor) (1) * Cancer, Ewings Sarcoma (6) * Cancer, Ovaries (1) * Cancer, Primary Neuroectodermal Tumor of the Spine (PNET) (2) * Cancer, Rhabdomyosarcoma (4)* Candida Yeast Infection (7) Carbamyl Phosphate Synthetase Deficiency (CPS) (2) * Carbohydrate-Deficient Glycoprotein Syndrome (CDGS) (8) * Carbon Monoxide Poisoning (2) Cardiac Pacemaker (23) Cardio-Facio-Cutaneous Syndrome (19) ** Cardiomyopathy (36) * www.childrenscardiomyopathy.org

55. Thyrolink - Recently Published Editions J Clin Endocrinol Metab 2000, 85 286 292. Mallory SB. Cowden Syndrome(multiple hamartoma syndrome). Dermatologic Clinics 1995, 13 27-31. http://www.thyrolink.com/literature/report2000_4/seite08.html

References Ball D.W., Baylin S.B., De Butros A.C. Medullary thyroid carcinoma, In : Werner and Ingbar’s The Thyroid, Eighth Edition. Braverman L.E. and Utiger R.E. (Eds). Lippincott-Williams-Wilkins, Philadelphia, 2000, 930- 943. Donovan D.T., Gagel R.F. Medullary thyroid carcinoma and the Multiple Endocrine Neoplasia Syndromes. In: Thyroid Diseases: endocrinology, surgery, nuclear medicine and radiotherapy, 2nd Edition, Falk. A (Ed) Lippincott-Raven. Philadelphia,1997: 619-644. Mathew C.G.P., Chin K.S., Easton D.F., Thorpe K., Carter C, Liou G.I., Fong S.L., Bridges C.D.B., Haak H, Nieuwenhuijzen Kruseman A.C., Schifter S., Hansen H.H, Telenius H., Telenius-Berg M., Ponder B.A.J. A linked genetic marker for multiple endocrine neoplasia type 2A on chromosome 10. Nature 1987, 328: 527-528. Simpson NE, Kidd KK, Goodfellow PJ, Mc Dermid H, Myers S, Kidd JR. Assignment of multiple endocrine neoplasia type 2A to chromosome 10 by linkage. Nature 1987, 328: 528-530. Donis-Keller H., Dou S., Chi D., Carlson K.M., Toshima K., Lairmore T.C., Howe J.R., Moley J.F., Goodfellow P., Wells S.A. Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC. Hum Mol Genet 1993, 2: 851-856. Hofstra R.M, Landsvater R.M., Ceccherini I., Stulp R.P., Stelwagen T., Luo Y., Pasini B., Hoppener J.W.M., Ploos Van Amstel H.K., Romeo G, Lips C.J.M., Buys C.H.C.M. Amutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma. Nature 1994, 367: 375-376.

56. Inflammatory Papillary Hyperplasia inflammatory papillary hyperplasia verruca vulgaris multiple squamous papillomasoral mucosal lesions of Cowden´s or multiple hamartoma syndrome lesions of http://www.dental.mu.edu/oralpath/lesions/flphyp/inflamhyperplasia.htm

Inflammatory Papillary Hyperplasia (Denture Papillomatosis) A reactive tissue growth that usually develops beneath a denture. Clinical Features: "raspbery" appearce (multiple small erythematous nodules) may become symptomatic with secondary infection of Candidia albicans occurs on the palate more common in patients who wear dentures continuously Differential Diagnosis: condyloma acuminatum inflammatory papillary hyperplasia verruca vulgaris multiple squamous papillomas pyostomatitis vegetans Tissue of Origin: mucosa Histologic Features: epithelium and connective tissue papillary configuration inflamed connective tissue inflammatory cells may penetrate epithelium Main Pathologic Process: benign hyperplasia and inflammation Treatment: removing appliances for prolonged periods of time and using tissue conditioner on the base of the dentures use of antifungal agent possible surgical intervention Prognosis: seldom resolves completely, fibrous tissue does not return to normal Webmaster © 2001 - Marquette University School of Dentistry - P.O. Box 1881 - Milwaukee, WI 53201-1881

57. Mioti: Medical Condition Condition Cowden Disease. Cowden Disease (multiple hamartoma syndrome).Information from eMedicine. Cowden disease and the PTEN gene. http://www.mioti.com/cat/condition/condition.asp?Cat=CowdenDisease

58. Hamartoma Syndrome, Multiple A collection of medical, dental and veterinary images for use in teaching. hamartoma syndrome, multiple http://www.brisbio.ac.uk/ROADS/subject-listing/hamartomasyndromemultiple.html

A collection of medical, dental and veterinary images for use in teaching. Home About the Archive FAQ Terms and Conditions ... Help Hamartoma Syndrome, Multiple Cowden's syndrome Cowden's syndrome Cowden's syndrome

59. Hamartome Multiple, Syndrome : Sites Et Documents Francophones Le mot clé hamartome multiple, syndrome hamartoma multiple, syndrome est présent au sein de plusieurs arborescences http://www.chu-rouen.fr/ssf/pathol/hamartomemultiplesyndrome.html

Hamartome Multiple, Syndrome Menu général CISMeF Synonyme(s) cowden, maladie ; maladie cowden ; syndrome hamartome multiple Arborescence(s) hamartome multiple, syndrome hamartoma multiple, syndrome maladies et malformations congénitales, héréditaires et néonatales tumeurs 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 : guide ressources Cowden, syndrome de - synonyme(s) et inclusion(s) : Hamartomes multiples [Par Dr Longy M, Dr Lasset C. Site éditeur Orphanet base de données sur les maladies rares et les médicaments orphelins. Direction Générale de la Santé / INSERM ; ; langue : français ; format : html ; accès : gratuit ; non parrainé ; daté de : 1999 ; visité le : 12/10/2000]. mots clés : * hamartome multiple, syndrome hamartome multiple, syndrome diagnostic type(s) : guide ressources structure recherche texte association patients 20 janvier 2003 courriel Menu général CISMeF Haut de page © CHU de Rouen . Toute utilisation partielle ou totale de ce document doit mentionner la source.

60. HON - List Of Rare Diseases Hallermann's syndrome, HallervordenSpatz syndrome. hamartoma syndrome, multiple,Hand-Schueller-Christian syndrome. Hartnup Disease, Hemoglobinuria, Paroxysmal. http://www.hon.ch/HONselect/RareDiseases/

List of rare diseases: English Deutsch Acrocephalosyndactylia Acrodermatitis ... HONewsletter http://www.hon.ch/HONselect/RareDiseases/index.html Last modified: Thu Sep 26 2002

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