1. EMedicine - Cowden Disease (Multiple Hamartoma Syndrome) : Article By Charles Mi Cowden Disease (multiple hamartoma syndrome) Cowden disease (CD), also termed Cowden syndrome and multiple hamartoma syndrome, is an autosomal dominant http://www.emedicine.com/DERM/topic86.htm

(advertisement) Home Specialties Resource Centers CME ... Patient Education Articles Images CME Patient Education Advanced Search Consumer Health Link to this site Back to: eMedicine Specialties Dermatology Internal Medicine Cowden Disease (Multiple Hamartoma Syndrome) Last Updated: July 10, 2002 Rate this Article Email to a Colleague Synonyms and related keywords: multiple hamartoma syndrome, Cowden syndrome AUTHOR INFORMATION Section 1 of 10 Author Information Introduction Clinical Differentials ... Bibliography Author: Charles Miller, MD , Dermatologist, Department of Dermatology, Southern California Kaiser Permanente Charles Miller, MD, is a member of the following medical societies: American Academy of Dermatology Editor(s): Craig A Elmets, MD , Director of Dermatology, Departments of Dermatology, Professor, Pathology, Environmental Health Sciences, The Kirklin Clinic, University of Alabama at Birmingham; Richard Vinson, MD , Chief, Department of Dermatology, William Beaumont Medical Center; Lester Libow, MD

2. EMedicine - Trichilemmoma : Article Excerpt By: William P Baugh, MD Jadassohn. When many trichilemmomas are present, Cowden disease (multiple hamartoma syndrome) should be suspected. The diagnosis http://www.emedicine.com/derm/byname/trichilemmoma.htm

(advertisement) Excerpt from Trichilemmoma Synonyms, Key Words, and Related Terms: tricholemmoma, benign neoplasms of the follicular epithelium, Cowden syndrome, Cowden’s syndrome, Cowden disease, Cowden’s disease, multiple hamartomas, multiple hamartoma syndrome, nevus sebaceous of Jadassohn Please click here to view the full topic text: Trichilemmoma Background: In 1962, Headington and French first described trichilemmoma as a benign neoplasm with differentiation toward pilosebaceous follicular epithelium. Subtle clinical and distinctive histologic features may characterize these superficial cutaneous tumors. Their significance resides in the association with Cowden disease and the need to differentiate trichilemmomas from other more aggressive cutaneous tumors. Clinically, trichilemmomas present as smooth, asymptomatic papules or verrucoid growths. They may occur as a solitary lesion or as multiple lesions, and they are usually found on the face (see Image 1 ). These lesions often mimic a basal cell carcinoma or a wart. Trichilemmoma should be considered in the differential diagnosis of any indistinct facial papule. Differentiation from a basal cell carcinoma or a trichilemmal carcinoma is needed for appropriate patient management. Trichilemmomas are often reported in association with a nevus sebaceous of Jadassohn. When many trichilemmomas are present, Cowden disease (multiple hamartoma syndrome) should be suspected. The diagnosis of trichilemmoma is usually obtained by microscopic examination, revealing distinct histologic features.

3. Multiple Hamartoma Syndrome Information Diseases Database multiple hamartoma syndrome,Cowden s syndrome,Dysplastic cerebellar gangliocytoma,LhermitteDuclos disease, Disease Database Information. http://www.diseasesdatabase.com/ddb31336.htm

Diseases Database Index Sponsors Contact ... Previous Page Multiple hamartoma syndrome Information Search 4 synonyms or equivalents were found. Multiple hamartoma syndrome aka/or Cowden's syndrome aka/or Dysplastic cerebellar gangliocytoma aka/or Lhermitte-Duclos disease may cause or feature (Follow link for list) may be a risk factor for (Follow link for list) may be allelic with (Follow link for list) belong(s) to the category of (Follow link for list) Multiple hamartoma syndrome: Definition(s) via UMLS Code translations and terms via UMLS Multiple hamartoma syndrome: specific sites Send Multiple hamartoma syndrome to medical search engines (JavaScript enabled browsers only) If your browser has no JavaScript you can still use these: Search using Internet medical databases Search using Internet search engines (non-specialist) We subscribe to the HONcode principles of the Health On the Net Foundation i-medicine.info - the evidence based medicine, informatics and audit portal Valid XHTML 1.0 Served 2004-06-03 00:43:31 Metadata Updated 2004-05-22

4. Cowdens Disease (Multiple Hamartoma Syndrome) - Eurorad - Clinical Case 2839 - R teaching files,radiology,Cowdens Disease (multiple hamartoma syndrome),Young man with long standing symptoms, gastrointestinal polyposis, goitre and skin http://www.eurorad.org/case.cfm?uid=2839

5. Multiple Hamartoma Syndrome - Eurorad - Clinical Case 920 - Resident teaching files,radiology,multiple hamartoma syndrome,History of insulin dependent diabetes mellitus complaints of a growing and painful lump in the right breast http://www.eurorad.org/case.cfm?uid=920

6. Multiple Hamartoma Syndrome Other characters, multiple hamartoma syndrome,. Print this article, see Cowden disease. ALB. The Encyclopaedia of Medical Imaging Volume IV1. http://www.amershamhealth.com/medcyclopaedia/medical/Volume IV 1/MULTIPLE HAMART

Amershamhealth.com Search for: Type a word or a phrase. All forms of the word are searchable. Browse entry words starting with: A B C D ... Other characters Multiple hamartoma syndrome, see Cowden disease ALB The Encyclopaedia of Medical Imaging Volume IV:1 Contacts GE Healthcare Making Waves

7. Hamartoma, Oesophageal In patients with multiple hamartoma syndrome they present as numerous very small sessile lesions causing a small sharply demarcated filling defect on double http://www.amershamhealth.com/medcyclopaedia/medical/Volume IV 1/HAMARTOMA OESOP

Amershamhealth.com Search for: Type a word or a phrase. All forms of the word are searchable. Browse entry words starting with: A B C D ... Other characters Hamartoma, oesophageal, benign tumour characterized histologically by metaplastic respiratory epithelium and islets of cartilage in a fibrous stroma. They can be solitary or may be multiple as part of the Cowden disease. Radiographically they have a variable appearance on the barium study of the oesophagus. The solitary form presents as a nonspecific intraluminal pedunculated and smoothly lined filling defect. In patients with multiple hamartoma syndrome they present as numerous very small sessile lesions causing a small sharply demarcated filling defect on double contrast barium study of the oesophagus. Also, see Cowden disease ALB The Encyclopaedia of Medical Imaging Volume IV:1 Contacts GE Healthcare Making Waves

8. HONselect - Hamartoma Syndrome, Multiple English Hamartoma Syndrome, Multiple, Cowden s Disease - multiple hamartoma syndrome - Cowden Disease - Cowdens Disease - Disease, Cowden - Disease, Cowden s. http://www.hon.ch/HONselect/RareDiseases/C04.445.435.html

List of rare diseases: English Deutsch Language: MeSH term: Accepted terms: English: Hamartoma Syndrome, Multiple - Cowden's Disease - Multiple Hamartoma Syndrome - Cowden Disease - Cowdens Disease - Disease, Cowden - Disease, Cowden's Français: HAMARTOME MULTIPLE, SYNDROME - COWDEN, MALADIE - MALADIE COWDEN - SYNDROME HAMARTOME MULTIPLE Deutsch: Cowden-Syndrom - Cowden-Krankheit - Multiple-Hamartome-Syndrom Español: SINDROME DE HAMARTOMA MULTIPLE - ENFERMEDAD DE COWDEN Português: SINDROME DO HAMARTOMA MULTIPLO - DOENCA DE COWDEN HONselect ressources Definition: Yes Articles: Yes Images: No News: No Conferences: No Clinical trials: Yes Web sites: English Yes Français Yes Deutsch No Español No Português No Home About us Site map Feedback ... HONewsletter http://www.hon.ch/HONselect/RareDiseases/C04.445.435.html Last modified: Wed Apr 28 2004

9. Entrez PubMed Cowden syndrome (multiple hamartoma syndrome). Female; Gingival Neoplasms/genetics; Gingival Neoplasms/pathology; Hamartoma Syndrome, Multiple/genetics; http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Abstra

10. Entrez PubMed multiple hamartoma syndrome with osteosarcoma. Female; Hamartoma Syndrome, Multiple/complications; Hamartoma Syndrome, Multiple/pathology*; http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Abstra

11. Hamartoma Syndrome, Multiple Cowden s Disease; multiple hamartoma syndrome; Cowden Disease; Cowdens Disease; Disease, Cowden; Disease, Cowden s; Syndrome, Multiple Hamartoma. http://medical.webends.com/kw/Hamartoma Syndrome, Multiple

Medical.WebEnds.com - Medical Terminology Dictionary A B C D ... Z WWW Medical.WebEnds.com Hamartoma Syndrome, Multiple A hereditary disease characterized by multiple ectodermal, mesodermal, and endodermal nevoid and neoplastic anomalies. Papules of the face and oral mucosa are the most characteristic lesion. Other changes occur in the skin , in the thyroid, the breast , the gastrointestinal system, and the nervous system Google links Processing time was 0.27982497215271 seconds.

12. ORPHANET - Rare Diseases - Orphan Drugs détaillée de la maladie,...... Printing version, DISEASE Cowden syndrome, Synonym(s) multiple hamartoma syndrome, ICD Q85.8, No description is available, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=201

13. Disease Directory : Cowden Syndrome (multiple Hamartoma Syndrome). Diseases Genetic Disorders Cowden Syndrome Cowden syndrome (multiple hamartoma syndrome). Title Cowden syndrome (multiple hamartoma syndrome). http://www.diseasedirectory.net/detailed/26326.aspx

Wednesday, June 02, 2004 Genetic Disorders Aarskog Syndrome Aase Syndrome Ablepharon-Macrostomia Syndrome ... Cowden Syndrome : Cowden syndrome (multiple hamartoma syndrome). Directory Listing Title: Cowden syndrome (multiple hamartoma syndrome). Description: Cowden syndrome (multiple hamartoma syndrome). Mallory SB. Department of Internal Medicine, Washington University School of Medicine, St. Louis, Missouri, USA. Date Added: 2/17/2004 10:37:54 AM URL:

14. Disease Directory : EMedicine - Cowden Disease (Multiple Hamartoma Syndrome) : A Diseases Genetic Disorders Cowden Syndrome eMedicine Cowden Disease (multiple hamartoma syndrome) Article Directory Listing. http://www.diseasedirectory.net/detailed/26315.aspx

Wednesday, June 02, 2004 Genetic Disorders Aarskog Syndrome Aase Syndrome Ablepharon-Macrostomia Syndrome ... Cowden Syndrome : eMedicine - Cowden Disease (Multiple Hamartoma Syndrome) : Article ... Directory Listing Title: eMedicine - Cowden Disease (Multiple Hamartoma Syndrome) : Article ... Description: Cowden Disease (Multiple Hamartoma Syndrome) - Cowden disease (CD), also termed Cowden syndrome and multiple hamartoma syndrome, is an autosomal dominant Date Added: 2/17/2004 10:37:53 AM URL: http://www.emedicine.com/DERM/topic86.htm

15. Penn State Faculty Research Expertise Database (FRED) Faculty Research Expertise Database. Hamartoma Syndrome, Multiple. Related Terms, Cowden s Disease, multiple hamartoma syndrome. Cowden Disease, Cowdens Disease. http://fred.hmc.psu.edu/ds/retrieve/fred/meshdescriptor/D006223

16. Bannayan Riley Ruvalcaba Syndrome Comparisons may be useful for a differential diagnosis multiple hamartoma syndrome, also known as Cowden disease, is an extremely rare inherited disorder http://www.bchealthguide.org/kbase/nord/nord1105.htm

document.write(''); var hwPrint=1; var hwDocHWID="nord1105"; var hwDocTitle="Bannayan Riley Ruvalcaba Syndrome"; var hwRank="1"; var hwSectionHWID="nord1105"; var hwSectionTitle=""; var hwSource="cn6.0"; var hwProdCfgSerNo="wsh_html_031_s"; var hwDocType="NORD"; National Organization for Rare Disorders, Inc. Bannayan Riley Ruvalcaba Syndrome Important 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. Synonyms BRRS Bannayan-Zonana syndrome (BZS) Riley-Smith syndrome Ruvalcaba-Myhre-Smith syndrome (RMSS) Macrocephaly, multiple lipomas, and hemangiomata Macrocephaly, pseudopapilledema, and multiple hemangiomata Disorder Subdivisions None Related Disorders List Information on the following diseases can be found in the Related Disorders section of this report: Multiple hamartoma syndrome (Cowden disease) Sotos syndrome Associated congenital disorders General Discussion Bannayan-Riley-Ruvalcaba syndrome is a rare inherited disorder characterized by excessive growth before and after birth; an abnormally large head (macrocephaly) that is often long and narrow (scaphocephaly); normal intelligence or mild mental retardation; and/or benign tumor-like growths (hamartomas) that, in most cases, occur below the surface of the skin (subcutaneously). The symptoms of this disorder vary greatly from case to case.

17. Gardner Syndrome (For more information on this disorder, choose Turcot as your search term in the Rare Disease Database.) multiple hamartoma syndrome, also known as Cowden http://www.bchealthguide.org/kbase/nord/nord152.htm

document.write(''); var hwPrint=1; var hwDocHWID="nord152"; var hwDocTitle="Gardner Syndrome"; var hwRank="1"; var hwSectionHWID="nord152"; var hwSectionTitle=""; var hwSource="cn6.0"; var hwProdCfgSerNo="wsh_html_031_s"; var hwDocType="NORD"; National Organization for Rare Disorders, Inc. Gardner Syndrome Important 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. Synonyms Bone Tumor-Epidermoid Cyst-Polyposis Familial Adenomatous Polyposis with Extraintestinal Manifestations FAPG GRS Intestinal Polyposis III Oldfield Syndrome Polyposis, Gardner Type Polyposis-Osteomatosis-Epidermoid Cyst Syndrome Disorder Subdivisions None Related Disorders List Information on the following diseases can be found in the Related Disorders section of this report: Familial Polyposis Peutz-Jeghers Syndrome Cronkhite-Canada Disease Turcot Syndrome General Discussion Gardner syndrome is a rare, inherited disorder characterized by multiple growths (polyps) in the colon (often 1,000 or more), extra teeth (supernumerary), bony tumors of the skull (osteomas), and fatty cysts and/or fibrous tumors in the skin (fibromas or epithelial cysts). Gardner syndrome is a variant of familial adenomatous polyposis, a rare group of disorders characterized by the growth of multiple polyps in the colon. Gardner syndrome is inherited as an autosomal dominant trait.

18. Diagnosis - Hypertrichosis Table Cowden syndrome, multiple hamartoma syndrome, 158350. Denervation, (Various), List. multiple hamartoma syndrome, Cowden syndrome, 158350. Neoplasm, (Various), List. http://www.keratin.com/ab/ab007.shtml

hypertrichosis table Home Forums Privacy Advertising ... Home On this page... Introduction List of disorders involving excess hair growth (hypertrichosis) as a secondary symptom List of disorders involving excess hair growth (hypertrichosis) as a primary symptom Introduction The tables below records disorders known to involve hypertrichosis. The first table lists disorders where hypertrichosis is a primary symptom. The second table lists disorders where hypertrichosis can be one of several symptoms. Typically the other symptoms are of greater concern and health/life threatening. The clinical distinction between hypertrichosis and hirsutism is that hypertrichosis involves hair growth on any hair bearing area of skin. The excess hair growth may induced by a wide variety of environmental or genetic factors. Hirsutism is the growth of hair in a secondary sexual characteristic pattern. In women hirsutism involves unwanted excess hair limited to regions including the mustache, beard, chest and/or escutcheon areas. Hirsutism is typically induced by hormonal imbalance, especially androgen excess. This is not necessarily a complete list of disorders involving hypertrichosis. Links to relevant web pages on the Online Mendelian Inheritance in Man (OMIM) web database are also given where possible.

19. Anais Brasileiros De Dermatologia - multiple hamartoma syndrome is reported. Keywords multiple hamartoma syndrome; Mouth diseases. INTRODUÇO. http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962003000200008&l

20. An. Bras. Dermatol.  Vol.78 no.2; Abstract: S0365-05962003000200008 ISSN 03650596. A case of Cowden s disease or multiple hamartoma syndrome is reported. Keywords multiple hamartoma syndrome; Mouth diseases. http://www.scielo.br/scielo.php?script=sci_abstract&pid=S0365-05962003000200008&

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