Extractions: HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS This Article Full Text (PDF) Submit a related Letter to the Editor Alert me when this article is cited ... Alert me if a correction is posted Services Email this article to a friend Similar articles in this journal Alert me to new issues of the journal Download to citation manager PubMed Articles by Cetta, F. Francesco Cetta Institute of Surgical Clinics University of Siena 53100 Siena, Italy Some papers and an Editorial recently published in JCEM have dealt with familial nonmedullary thyroid carcinoma ( ). In particular, the paper by Stratakis et al. ) described two patients with thyroid carcinoma (one papillary, one follicular) as a candidate component of the Carney syndrome, an autosomal dominant genetic disease, characterized by spotty skin pigmentation, mixomas, primary pigmented nodular adrenocortical disease, and endocrine overactivity of other glands (pituitary, testis, ovary, breast). Thyroid
Cowdenin Tauti - Kehitysvammahuollon Tietopankki Cowden Disease (multiple hamartoma syndrome), eMedicine, Charles Miller multiple hamartoma syndrome (Cowden s disease) associated with nonHodgkin s http://www.saunalahti.fi/kup/syndroma/cowden.htm
Extractions: Multippeli hamartooma-oireyhtymä Genetics Home Reference -sivulla (2005) kerrottiin, että oireyhtymä on perinnöllinen häiriötila, jota luonnehtivat hamartoomaksi sanotut kasvamat ja lisääntynyt syöpäriski. Pienet kasvamat esiintyvät iholla ja limakalvoissa. Syöpä saattaa puhjeta rinnoissa, kilpirauhasessa ja kohdussa. Muita oireita voivat olla suurikokoinen pää, Lhermitte-Duclosin taudiksi nimitetty aivokasvain ja kehitysvammaisuus. Oireyhtymän esiintyvyydeksi mainittiin 1/200.000. Charles Miller kirjoitti eMedicine -artikkelissaan (2004), että iho-oireita oli ollut 90-100%:lla ja kilpirauhasoireita 66%:lla, etenevää suuripäisyyttä ( makrokefalia ) 80%:lla, silmien kasvaimia 13%:lla, rintasyöpää ( carcinoma of the breast ) 20-36%:lla 38-46-vuotiaista naisista (rintojen kyhmyjä oli ollut 75%:lla) ja paksusuolen epämuodostumia 72%:lla. Suun alueen 1-3 mm pinnallisia papuloita oli esiintynyt n. 80%:lla. Muina oireina mainittiin lintumaiset kasvot, pieni leuka ja korkea kitalaki. OMIM-tietokannan COWDEN DISEASE -artikkelin kliinisessä tiivistelmässä (2001) mainittiin, että keskitasoisesta lievään vaihtelevaa
Extractions: Hamartoma Syndrome, Multiple Definition: 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.
Extractions: 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. Synonyms and Source Vocabularies:
Kprones CowdenID10018 Cowden s disease (multiple hamartoma and neoplasia syndrome) a case report andreview of the English literature. Salem OS, Steck WD. http://www.infobiogen.fr/services/chromcancer/Kprones/CowdenID10018.html
Extractions: Home Genes Leukemias Solid Tumours ... NA Identity Other names Multiple hamartoma syndrome Inheritance autosomal dominant; high penetrance (close to 100% by the age of 30 yrs); highly variable expressivity (between and within families) Clinics Phenotype and clinics clinical manifestations usually occur during the 2nd and 3rd decade; they are dystrophic, hamartomatous or tumoral lesions including the following to variable extend: Overlapping syndromes Bannayan-Riley-Ruvalcaba syndrome including precocious stigmata of Cowden disease (macrocephaly, lipomas, genital pigmented macules, hamartomatous intestinal tract polyps) is considered as a pediatric form of Cowden disease Lhermitte Duclos syndrome or dysplastic gangliocytoma of the cerebelum is a rare and complex hamartomatous condition of the cerebellum which can occur alone but also in association with Cowden disease juvenile polyposis and Peutz Jeghers syndrome : Cowden disease, by its intestinal tract lesions can be linked to the scope of hereditary hamartomatous polyposis; molecular diagnosis can be useful in distinguishing juvenile polyposis, Peutz Jeghers syndrome or Cowden disease/Bannayan
Extractions: Home Genes Leukemias Solid Tumours ... NA Identity Other names Bannayan-Zonana syndrome Riley-Smith syndrome Ruvalcaba-Myhre-Smith syndrome Macrocephaly, pseudopapilledema, multiple hemangiomata Macrocephaly, multiple lipomas, hemangiomata Inheritance autosomal dominant; existence of sporadic cases Clinics Note Bannayan-Riley-Ruvalcaba syndrome is an overgrowth syndrome / hamartomatous polyposis condition with an increased risk of benign and malignant tumours; other overgrowth syndromes at (known) risk of tumourigenesis are : Beckwith-Weideman syndrome Sotos syndrome (cerebral gigantism) Hemihyperplasia (hemihypertrophy), and Simpson Golabi Behemel syndrome Phenotype and clinics onset in chilhood (in contrast with Cowden disease , although an allelic disorder, see below); more often found in male patients (lower penetrance in female patients).
Extractions: Women's Health I've divided this page into two sections. The first provides you with some tips on searching for material on Medline, and the second provides links to other Australian and overseas web resources, including some full text report and journal literature. You will find material on cancer in Medline, but you will need to be aware of the thesaurus (MeSH) terms used to search for topics in this area. For example, if you look up the term Cancer in the Medline Thesaurus you will find the following. Cancer is not a MeSH term, but it is associated with the MeSH term Neoplasms In other words Medline does not use the word "cancer" in its list of terms. You will need to search the word "neoplasms". This term has an extensive number of more specific terms associated with it.
All Lipid Phosphatases Bannayan Zonana syndrome, BZS, ITGA 2, MGC11227, MHAM, MMAC1, multiple hamartoma Reacts with Mouse. Predicted to react with Human (100% identity with http://www.abcam.com/?c=2146
MeSH-D Terms Associated To MeSH-C Term Hamartoma Syndrome, Multiple MeSHD terms associated to MeSH-C term hamartoma syndrome, multiple, G2D Home the association of the corresponding term to hamartoma syndrome, multiple. http://www.bork.embl-heidelberg.de/g2d/c2d.pl?Hamartoma_Syndrome,_Multiple:unkno
Bannayan-zonana1999.html MINOR MESH HEADINGS hamartomasyndrome,-multiple-pathology; Head-pathology.MAJOR MeSH HEADINGS *hamartoma-syndrome,-multiple-genetics; http://www.indiana.edu/~pietsch/bannayan-zonana1999.html
Extractions: also called Bannayan-Riley-Ruvalcaba syndrome Record 1 of 6 in MEDLINE EXPRESS (R) 1999/11-1999/12 TITLE: Screening SMAD1, SMAD2, SMAD3, and SMAD5 for germline mutations in juvenile polyposis syndrome. AUTHOR(S): Bevan-S; Woodford-Richens-K; Rozen-P; Eng-C; Young-J; Dunlop-M; Neale-K; Phillips-R; Markie-D; Rodriguez-Bigas-M; Leggett-B; Sheridan-E; Hodgson-S; Iwama-T; Eccles-D; Bodmer-W; Houlston-R; Tomlinson-I ADDRESS OF AUTHOR: Section of Cancer Genetics, Haddow Laboratories, Institute of Cancer Research, Sutton, UK. SOURCE (BIBLIOGRAPHIC CITATION): Gut. 1999 Sep; 45(3): 406-8 INTERNATIONAL STANDARD SERIAL NUMBER: 0017-5749 PUBLICATION YEAR: 1999 LANGUAGE OF ARTICLE: ENGLISH COUNTRY OF PUBLICATION: ENGLAND MINOR MESH HEADINGS: Adolescence-; Genetic-Markers; Phosphoproteins-genetics; Polymorphism-Genetics; Trans-Activators-genetics
Clinica De Ortodoncia Dr. Arthur Nouel Is also known as multiple hamartoma and neoplasia syndrome. It is characterizedorally by the appearance of multiple lesions which are very similar to http://www.infocompu.com/adolfo_arthur/ingles/s_cowden.htm
Extractions: Portal de ortodoncia y enfermedades de la boca Home Virtual visit Clinic profile Our procedures Services Orthodontics Radiographs Diagnosis Educational Clinical cases Oral diseases Maxillofacial surgery Oral surgery Radiology Index News Products we use Te invitamos a visitar la sección de Cirugía Bucal, con las técnicas quirúrgicas más comunes de la especialidad. oral diseases Is also known as multiple hamartoma and neoplasia syndrome. see other photographs Home Virtual visit Clinic profile ... News
Hamartoma Syndrome, Multiple Terms And Definitions At Www hamartoma syndrome, multiple Definitions and Terms. MedicalGlossary.org is designedas a free, browsable resource for all. The medical terms and definitions http://www.medicalglossary.org/hamartoma_hamartoma_syndrome_multiple_definitions
Extractions: Definition: 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. Notes: do not use /blood supply /chem /second /secret /ultrastruct Previously Indexed: Hamartoma (1966-1986),Neoplasms, Multiple Primary (1966-1986) MedicalGlossary.org is designed as a free, browsable resource for all. The medical terms and definitions are not intended to replace medical informaion provided by licensed healthcare professionals. Please see a doctor if you need medical assistance. Don't see the medical term you were researching? Send us an e-mail from our "about us" page. We will do our best to research and classify new medical terms in a timely manner. Our current list of medical terms is over 26,000. Data sources include the U.S. National Library of Medicine, 2004 Medical Subject Headings. About Us Link to Us Main Categories: Anatomy Organisms Diseases Chemicals and Drugs ... Analytical, Diagnostic and Therapeutic Techniques and Equipment
La Maladie De Cowden multiple hamartoma and neoplasia syndrome). A case report andreview of the English literature. J Am Acad Dermatol 1983; 8 686-696. http://www.orpha.net/data/patho/FR/fr-cowden.html
Extractions: PTEN PTEN 1. Bonneau D and Longy M. Mutations of the human PTEN gene. Hum Mutat 2. Bronstein MH, Wolf M, Birowski JB. Cowden's disease: a cutaneous marker of breast cancer. Cancer 3. Erbe KW and Compton CC. Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 24-1987. A 56-year-old man with a substernal goiter, multiple cutaneous and mucosal lesions, and a positive stool test for occult blood. N Eng J Med 4. Fackenthal JD, Marsh DJ
Lentigo Carney complex in a patient with multiple blue naevi and lentigines, The classic hamartoma syndromes and the related conditions discussed in this http://www.thedoctorsdoctor.com/diseases/lentigo.htm
Extractions: Background This is a common and benign pigmented lesion of the skin, composed of an increase in melanocytes at the dermal-epidermal junction. It is closely related to the melanocytic nevus and indeed, some junctional nevi share histologic features with lentigos, occasionally called jentigos. OUTLINE Epidemiology Disease Associations Pathogenesis Laboratory/Radiologic/Other Diagnostic Testing ... Internet Links EPIDEMIOLOGY CHARACTERIZATION INCIDENCE Common AGE RANGE-MEDIAN All SEX (M:F) Both DISEASE ASSOCIATIONS CHARACTERIZATION CARNEY COMPLEX Carney complex: in a patient with multiple blue naevi and lentigines, suspect cardiac myxoma. Bleasel NR, Stapleton KM. Department of Dermatology, Royal Hobart Hospital, Tasmania, Australia. Australas J Dermatol 1999 Aug;40(3):158-60 Abstract quote Carney complex is characterized by spotty pigmentation (blue naevi and lentigines), myxomas (cardiac, cutaneous, mammary), endocrine over-activity (Cushing's syndrome, acromegaly), testicular tumours, and schwannomas. We report a male with multiple blue naevi, lentigines, testicular large cell calcifying Sertoli-cell tumour and four cardiac myxomas. The myxomas caused two cerebrovascular accidents and a myocardial infarction. All patients with multiple blue naevi or lentigines should be investigated for the life-threatening association of cardiac myxomas.
Birth Disorder Information Directory - M multiple Epiphyseal Dysplasia. See Beighton Goldberg Hoff syndrome. multipleHamartoma syndrome. See Cowden syndrome. multiple Hereditary Exostoses http://www.bdid.com/defectm.htm
Extractions: HOME Machado Joseph Disease (Autosomic Dominant Spinocerebellar Ataxia, Autosomic Dominant Cerebellar Ataxia, Cerebelloolivary Atrophy, Olivopontocerebellar Atrophy, Pierre Marie Cerebellar Ataxia) Macrencephaly Macrocephaly Macrodactyly/Megalodactyly Macroglossia Macrogyria Macular Dystrophy Macules Madelung's Deformity Majewski Syndrome Mal de Meleda Male Pseudohermaphroditism Due to Androgen Insensitivity Male Turner Syndrome Malignant Hyperthermia See Hyperthermia, Malignant
