41. CancerGene MHAM Name, multiple hamartoma (Cowden syndrome). Locus, 10q22q23. OMIM, 158350, OMIM Title COWDEN DISEASE; CD; COWDEN SYNDROME; CS; multiple hamartoma syndrome; MHAM; http://caroll.vjf.cnrs.fr/cancergene/CG73.html

Infobiogen Search CancerGene CancerGene Homepage Search CancerGene Citations CancerGene Card Symbol MHAM Aliases Name multiple hamartoma (Cowden syndrome) Locus OMIM GDB SwissProt LocusLink MHAM Class DISORDER Diseases Hamartoma Syndrome, Multiple; Neoplastic Syndromes, Hereditary Note For germline mutations in MHAM see the gene PTEN ( CG:639 Selected MEDLINE References: [Link to NCBI] [Link to CancerGene Citation Database] Recent Articles : Kwon CH;Zhu X;Zhang J;Knoop LL;Tharp R;Smeyne RJ;Eberhart CG;Burger PC;Baker SJ Pten regulates neuronal soma size: a mouse model of Lhermitte-Duclos disease. Nat Genet 2001 Dec;29(4):404-11. Backman SA;Stambolic V;Suzuki A;Haight J;Elia A;Pretorius J;Tsao MS;Shannon P;Bolon B;Ivy GO;Mak TW Deletion of Pten in mouse brain causes seizures, ataxia and defects in soma size resembling Lhermitte-Duclos disease. Nat Genet 2001 Dec;29(4):396-403. Fackenthal JD;Marsh DJ;Richardson AL;Cummings SA;Eng C;Robinson BG;Olopade OI Male breast cancer in Cowden syndrome patients with germline PTEN mutations. J Med Genet 2001 Mar;38(3):159-64.

42. NEJM -- Hereditary Gastrointestinal Polyposis And Nonpolyposis Syndromes PeutzJeghers Syndrome. Juvenile Polyposis. Cowden s Disease (multiple hamartoma syndrome). Neurofibromatosis. Hereditary Nonpolyposis Colorectal Cancer Syndromes. http://content.nejm.org/cgi/content/short/331/25/1694

HOME SEARCH CURRENT ISSUE PAST ISSUES ... HELP Please sign in for full text and personal services Previous Volume 331:1694-1702 December 22, 1994 Number 25 Next Hereditary Gastrointestinal Polyposis and Nonpolyposis Syndromes Anil K. Rustgi Since this article has no abstract, we have provided an extract of the first 100 words of the full text and any section headings. Full Text Letters Add to Personal Archive Add to Citation Manager ... PubMed Citation Colon cancer is one of the most frequent cancers in men and women in the United States. There is a 6 percent lifetime risk of colon cancer in the general population. Approximately 160,000 new cases arise every year, and despite advances in detection and therapy, 60,000 people die of colon cancer and its complications each year. Epidemiologic studies have implicated environmental factors in the pathogenesis of the disease. Support for these findings comes from the wide variations in the incidence of colon cancer among different populations. In Western societies, with diets high in fat and low Full Text of this Article Gastrointestinal Polyposis and Nonpolyposis Syndromes Adenomatous Polyposis Syndromes Familial Adenomatous Polyposis Genetic Features of Familial Adenomatous Polyposis Gardner's Syndrome Screening of Kindreds with Familial Adenomatous Polyposis and Gardner's Syndrome Turcot's Syndrome Hamartomatous Polyposis Syndromes Peutz-Jeghers Syndrome Juvenile Polyposis Cowden's Disease (Multiple Hamartoma Syndrome) Neurofibromatosis Hereditary Nonpolyposis Colorectal Cancer Syndromes

43. :: Ez2Find :: M Cancer (22), Moyamoya Disease (6) MPS III (6) MRKH (8) Mucopolysaccharidosis 3 (6) Multiple Chemical Sensitivity (28) multiple hamartoma syndrome (3) Multiple http://ez2find.com/cgi-bin/directory/meta/search.pl/Health/Conditions_and_Diseas

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44. PhosphaBase MMAC1;;PHOSPHATASE AND TENSIN HOMOLOG DELETED ON CHROMOSOME 10 158350 COWDEN DISEASE; CD;;COWDEN SYNDROME; CS;;multiple hamartoma syndrome; MHAM;DYSPLASTIC http://bioinf.man.ac.uk/phosphabase/tyrdisease.html

Home About PhosphaBase Tutorial and Examples Status ... Contact News and Views Conferences and Meetings Phosphatase of the Month Phosphatase Publications Positions A Protein Phosphatase Information Resource Tyrosine Phosphatases Implicated in Disease

45. Cowden Tellmeabout.co.uk eMedicine Cowden Disease (multiple hamartoma syndrome) Article Cowden Disease (multiple hamartoma syndrome) - Cowden disease (CD), also termed Cowden http://www.tellmeabout.co.uk/directory/c/cowden/readme.htm

46. Displaying Medical Dictionary Terms Starting With Letter MU multiple exostosis multiple fission multiple fracture multiple gestation multiple glandular deficiency syndrome multiple hamartoma syndrome multiple idiopathic http://www.books.md/M/MU.php

Home M /MU Medical Dictionary Search Engine Advertise on this site! A service of health-link-net.com Browse Dictionary Alphabetically A B C D ... Z Displaying all terms starting with letter MU mu mucamide mucase mucate ... Home

47. Blackwell Synergy - Cookie Absent 6, Mallory SB (1995). Cowden syndrome (multiple hamartoma syndrome). Early diagnosis of multiple hamartoma and neoplasia syndrome the role of the dentist. http://www.blackwell-synergy.com/links/doi/10.1034/j.1601-0825.2001.00679.x/enha

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48. Blackwell Synergy - Cookie Absent Sir, Cowden s disease (CD), or multiple hamartoma syndrome, is an uncommon autosomal dominant condition characterized by multiple hamartomas. http://www.blackwell-synergy.com/links/doi/10.1111/j.1365-2133.2003.05770.x/full

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49. Cowden Syndrome - Genetics Home Reference Genetic disorder catalog. What other names do people use for Cowden syndrome? Cowden s disease; Cowden s syndrome; CS; MHAM; multiple hamartoma syndrome. http://ghr.nlm.nih.gov/condition=cowdensyndrome

A service of the U.S. National Library of Medicine Home Search Conditions Genes ... Help Cowden syndrome Related Gene(s) Quick links to this topic NIH Publications National Institutes of Health MedlinePlus Health Information Patient support For patients and families Gene Reviews Clinical summary Gene Tests DNA test labs ClinicalTrials.gov Research studies PubMed Recent literature OMIM Genetic disorder catalog Cowden syndrome What is Cowden syndrome? Cowden syndrome is an inherited disorder characterized by multiple tumor-like growths (called hamartomas) and an increased risk of certain cancers. Almost everyone with this condition has hamartomas. These small, noncancerous growths are most commonly found on the skin and mucous membranes (such as the lining of the mouth and nose), but can also occur in the intestinal tract and other parts of the body. People with Cowden syndrome have an increased risk of developing several types of cancer, including cancers of the breast, thyroid, and uterus. Noncancerous breast and thyroid disease are also common. Other symptoms of Cowden syndrome can include an enlarged head; a rare, noncancerous brain tumor called Lhermitte-Duclos disease; and mental retardation. How common is Cowden syndrome?

50. Mu : On Medical Dictionary Online Dysplasias Multiple Exostoses Multiple Exostoses, Hereditary Multiple Exostosis Multiple Exostosis, Hereditary multiple hamartoma syndrome Multiple Head http://www.online-medical-dictionary.org/?q=~Mu

51. Cowden's Syndrome malignant transformation. Synonyms multiple hamartoma syndrome. ICD9-CM 759.6 other hamartoses, NEC Author(s) Mark R. Dambro, MD http://www.5mcc.com/Assets/SUMMARY/TP0234.html

Cowden's syndrome DESCRIPTION: Autosomal dominant hereditary disease. Characteristics - ectodermal neoplasia, microstomia, trichilemmomas of the face, acral verrucous papules. Usual course - chronic; progressive. CAUSES: ectodermal neoplasia mesodermal neoplasia malignant transformation Synonyms: multiple hamartoma syndrome ICD-9-CM: 759.6 other hamartoses, NEC Author(s): Mark R. Dambro, MD

52. Www.nlm.nih.gov/cgi/mesh/2K/MB_cgi?term=Hamartoma+Syndrome,+Multiple Genetics of PTEN in Cowden Syndrome and Sporadic Breast Cancer International Cowden Consortium. CS is an inherited multiple hamartoma syndrome with a high risk of breast and thyroid cancer. The PT has http://www.nlm.nih.gov/cgi/mesh/2K/MB_cgi?term=Hamartoma Syndrome, Multiple

53. Health, Conditions And Diseases, Genetic Disorders: Cowden Syndrome Cowden disease (CD), also termed Cowden syndrome and multiple hamartoma syndrome, is an autosomal dominant condition with variable expression that results from http://www.combose.com/Health/Conditions_and_Diseases/Genetic_Disorders/Cowden_S

Top Health Conditions and Diseases Genetic Disorders ... Cowden Syndrome Related links of interest: Health:Conditions and Diseases:Rare Disorders Cowden Syndrome - A CHORUS notecard document about this syndrome. Cowdens Syndrome Support Group - Offers information and message boards for families and patients affected by the disease. Emergency Medicine - A introduction of Cowden disease followed by an in depth report, including treatment, medication and follow up. Cowden disease (CD), also termed Cowden syndrome and multiple hamartoma syndrome, is an autosomal dominant condition with variable expression that results from a mutation in the PTEN gene on chromosome arm 10q, as reported by Liaw et al. CD causes hamartomatous neoplasms of the skin and mucosa, GI tract, bones, central nervous system (CNS), eyes, and genitourinary tract. Skin is involved in 90-100% of cases; the thyroid in 66%. Help build the largest human-edited directory on the web. Submit a Site Open Directory Project Become an Editor The combose.com directory is based on the Open Directory and has been modified and enhanced using our own technology.

54. SearchBug Directory: Health: Conditions_and_Diseases: M Motion Sickness (6), Mouth Cancer (23) Moyamoya Disease (6) MPS III (6) MRKH (10) Multiple Chemical Sensitivity (28) multiple hamartoma syndrome (3) Multiple http://www.searchbug.com/directory.aspx/Health/Conditions_and_Diseases/M/

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55. Favorites Acute hemorrhagic pancreatitis Acute pancreatitis PeutzJeghers syndrome Biliary ascariasis Cowdens Disease (multiple hamartoma syndrome) CT evaluation of http://www.radquiz.com/favorites.htm

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57. Karger Publishers an uncommon, peculiar type of predominantly collagenous fibroma that was first reported as a component of Cowden s disease (multiple hamartoma syndrome) 1, 2 http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowFulltext&ProduktNr=

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59. Bini Et Al.: Multiple Chondromatous Hamartomas... Cowden disease is a multiple hamartoma syndrome characterized by mucocutaneous lesions, multiple benign tumors of internal organs and increased risk for breast http://www1.elsevier.com/gej-ng/10/22/71/61/52/31/article.html

Interactive Cardiovascular and Thoracic Surgery, Vol. 1 (2) (2002) pp. 78-80 PII: S1569-9293(02)00058-0 Case report Multiple chondromatous hamartomas of the lung A. Bini, M. Grazia, F. Petrella fpetrella@libero.it and M. Chittolini Department of General and Thoracic Surgery, University of Bologna, S. Orsola - Malpighi Hospital, Bologna, Italy Received 12 June 2002; received in revised form 21 August 2002; accepted 26 August 2002 Abstract Multiple chondromatous hamartomas (MCH) of the lung are very rare: only 16 cases have been reported to date. In young women, the tumours may be a manifestation of Carney triad (gastric leiomyoblastoma, pulmonary hamartoma and extra-adrenal paraganglioma) or Cowden syndrome (mucocutaneous lesions, multiple benign tumors of internal organs and increased risk for breast, thyroid, urogenital and digestive tract cancer). We report the 17th case of MCH of the lung, diagnosed accidentally in a 66 year-old male patient, with suspected concomitant hamartomas and malignant tumours. Keywords: Multiple chondromatous hamartomas of the lung Carney triad Cowden syndrome Corresponding author. Tel.: +39-338-823-1311

60. Article : Radiological Quiz - Neuroradiology ; Author : SUREKHA K ; Co-Author(s) leontiasis ossea. Coexisting conditions in LDD include Cowden s disease, which is also called multiple hamartoma syndrome. It is http://www.ijri.org/articles/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.

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