Bz-update.html This group of syndromes includes PeutzJeghers, multiple hamartoma, juvenilepolyposis, Cronkhite-Canada, and Bannayan-Riley-Ruvalcaba. http://www.indiana.edu/~pietsch/bz-update.html
Extractions: also called Bannayan-Riley-Ruvalcaba syndrome MEDLINE EXPRESS (R) 1/96-1/97 1 of 13 TI: Clinicopathologic findings in the Bannayan-Riley-Ruvalcaba syndrome. AU: Fargnoli-MC; Orlow-SJ; Semel-Concepcion-J; Bolognia-JL AD: Department of Dermatology, Yale University School of Medicine, New Haven, Conn, USA. SO: Arch-Dermatol. 1996 Oct; 132(10): 1214-8 ISSN: 0003-987X PY: 1996 LA: ENGLISH CP: UNITED-STATES MESH: Abnormalities,-Multiple-genetics; Adolescence-; Adult-; Bone-and-Bones-abnormalities; Head-abnormalities; Mental-Retardation-genetics; Skin-pathology; Skin-Diseases-genetics; Skin-Diseases-pathology; Syndrome- MESH: *Abnormalities,-Multiple; *Mental-Retardation; *Skin-Diseases TG: Case-Report; Female; Human; Male
Extractions: This survey of medical eponyms and the persons behind them is meant as a general interest site only. No information found here must under any circumstances be used for medical purposes, diagnostically, therapeutically or otherwise. If you, or anybody close to you, is affected, or believe to be affected, by any condition mentioned here: see a doctor. Achondromatosis with haemangiomata, chondrodysplasia angiomatosis syndrome, chondrodystrophy-haemangiomas syndrome; chondrodystrophy and vascular hamartoma syndrome, chondrodystrophy with angiomatosis, chondrodystrophy with vascular hamartoma, cutaneous dyschondroplasia-dyschromia syndrome, dyschondroplasia-angiomatosis syndrome, dyschondroplasia with haemangioma, dyschondrodysplasia-haemangiomas syndrome; multiple enchondromatosis syndrome; vascular hamartoma-dyschondroplasia syndrome. Syndrome of enchondromas (benign tumours of cartilage), associated with multiple cavernous haemangiomas. Sometimes the patients show pigmentation. Normal at birth; bone and cartilage deformities appear during childhood in the years before puberty and the deformities increase during the period of growth. Complications are pathological fractures and other disorders of nonossified cartilage in the metaphyses and diaphyses of the long bones, chondrosarcoma and angiosarcoma. The skin and bony elsions are asymmetrical and do not coincide anatomically. Usually, no history of pain; orthostatic hypotension in sitting or standing position. Normal intelligence. Males are more frequently affected. Both sexes affected. Most cases are sporadic, but some instances of familial occurrence have been reported.
Extractions: 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
Radiology -- Table Of Contents (137 [2]) H Hauser, B Ody, O Plojoux, and P Wettstein Radiological findings in multiplehamartoma syndrome (Cowden disease) a report of three cases http://radiology.rsnajnls.org/content/vol137/issue2/
Extractions: [Search ALL Issues] To see an article , click its [Full Text] link. To review many abstracts , check the boxes to the left of the titles you want, and click the 'Get All Checked Abstract(s)' button. To see one abstract at a time , click its [Abstract] link. SH Levitt Erskine Memorial Lecture, 1979. In memory of Arthur W. Erskine, M.D. Introduction of the orator, Luther W. Brady, M.D
FSP Syndromes Clinical Pure spastic paraparesis, or Complicated syndromes Other COL9A3mutations cause multiple epiphyseal dysplasia, Type3 http://www.neuro.wustl.edu/neuromuscular/spinal/fsp.html
