Extractions: Bannayan-Riley-Ruvalcaba syndrome,BRRS,Bannayan-Zonana syndrome (BZS),Riley-Smith syndrome,Ruvalcaba-Myhre-Smith syndrome (RMSS),Macrocephaly with multiple lipomas and hemangiomata,Macrocephaly with pseudopapilledema and multiple hemangiomata For Information on Workshops and Seminars for Special Needs Children click here The GAPS INDEX 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. In most cases, infants with Bannayan-Riley-Ruvalcaba syndrome exhibit increased birth weight and length. As affected infants age, the growth rate slows and adults with this disorder often attain a height that is within the normal range.
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.
Diagnosis And Discussion Follicular Hamartoma of the BirtHogg-Dube syndrome are characterized by multiple papular lesions Some of the lesions of the follicular hamartoma syndromes are also characterized by http://www.xmission.com/~bweems/bhddxdis.html
Extractions: DISCUSSION The stromal component of this unusual lesion is modified perifollicular connective tissue. The hair papilla is a special modification of the same mesenchyme. A natural representation of such mesenchyme might be found in a site in which a hair bulb has undergone cytolysis and the immediately adjacent tissue, including the papilla and the connective tissue sheath, has responded by becoming sclerotic ( Fig 10 At least a part of the lesion in question has features of a fibrofolliculoma as seen in the Birt-Hogg-Dube syndrome. Patterns of a characteristic example of the papular and polypoid lesions of the follicular hamartoma syndrome are represented in figs 11- 16 . In Fig 11 , three follicles are represented in cross section. The red arrow points to a follicle showing the pattern of fibrofolliculoma with mantle-like patterns and perifollicular fibrosis. The green arrows identify follicles that are not significantly distorted in the plane of the section but there is perifollicular fibrosis (perifolliculoma pattern). A sebaceous gland is associated with the follicle on the right. The lesion in fig 12 is slightly polypoid. The pattern is mantle-like with perifollicular fibrosis and sebaceous gland lobules (fibrofolliculoma pattern). The lesion in
Extractions: Unfortunately we have collected way too many articles and too much information to affordably publish on one website. Eventually we hope to make all of these available for download from this site. We would like to get this information to you now if you desire. Here is an example of a collection of over 1200 articles and abstracts that have been organized and sorted by manifestation and date. Each category contains a summary of the information along with links to websites with articles and information, definitions of the pertinent terms. Many are full text articles. PDF available for many as well. Dozens of quality photos. Main points of the articles and summary's are highlighted in yellow. This is a great reference tool or resource for you and your health care providers. The entire collection is available on CD Rom. For more information contact the Nevoid Basal Cell Carcinoma Syndrome / Gorlin Syndrome Patient Advocate or you may request a copy of the CD from our Registration Page with articles in either Microsoft Word or soon in Microsoft Works Format. You will be notified of updates if you are a registered member.
MeSH-D Terms Associated To MeSH-C Term Hamartoma Syndrome MeSHD terms associated to MeSH-C term hamartoma syndrome, multiple, G2D Home. The number indicates the strength of the association http://www.bork.embl-heidelberg.de/g2d/c2d.pl?Hamartoma_Syndrome,_Multiple:unkno
Extractions: Extracted from IndMED Khatri ML; Shafi M; Sen NK Departments of Dermatology and Pathology, Faculty of Medicine, A1-Fateh University of Medical Sciences, Tripoli, Libya. Cowden's disease. Indian Journal of Dermatology, Venereology and Leprology. 1996 Sep-Oct; 62(5): 322-4 ABSTRACT: A 24-year-old male patient developed multiple lesions of keratoacanthoma in the epidermal verrucous naevus. He also had multiple papillomatous lesions on the lips, buccal mucosa, gingiva and tongue, with positive family history of similar lesions. He also had multiple skin tags and patchy palmoplantar keratoderma and minimal kyphoscoliosis. KEYWORDS: Hamartoma Syndrome, Multiple/GE; Hamartoma Syndrome, Multiple/PA; Hamartoma Syndrome, Multiple/DI; Meningeal Neoplasms/PA; Neoplasms/ET; Skin Neoplasms/GE; Skin Neoplasms/DI; Skin/PA; Keratoacanthoma/DI; Keratoacanthoma/GE; Neoplasms, Multiple Primary/GE; Papilloma/DI; Adult; Human; Male; Case Report OTHER KEYWORDS: Histopathology References: 6 Record Identifier: TB3765
Clinica De Ortodoncia Dr. Arthur Nouel oral diseases. Cowdens syndrome. Is also known as multiple hamartoma and neoplasia syndrome. It is characterized orally by the 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
New Page 1 Directory Results for M assoicated to Health from Linkspider.org. Keyword Search M assoicated to Health. Search and Browse Information http://www.linkspider.org/index.cgi/Health/ConditionsandDiseases/M/
Extractions: Keyword Search: M assoicated to Health Search For: Match » -All words -Any word -Exact text Content » The Web Jobs / Vacancy Images / Photos FTP / Downloads United Kingdom United States of America Argentina Austria Australia Bangladesh Belgium Bolivia Brazil Bulgaria Canada Chile China Cuba Cyprus Czech Republic Czechoslovakia Denmark Dominican Republic Ecuador Egypt Estonia Finland France Germany Ghana Greece Hong Kong Hungary Iceland India Indonesia Ireland Israel Italy Japan Jordan Kenya Kuwait Latvia Lithuania Luxembourg Malaysia Malta Mexico Moldavia Monaco Morocco Mozambique Nepal Netherlands New Zealand Nicaragua Nigeria North Korea Norway Pakistan Panama Paraguay Peru Philippines Poland Portugal Qatar Romania Russian Federation Saudi Arabia Singapore South Africa South Korea Spain Sri Lanka Sweden Switzerland Taiwan Tanzania Thailand Tunisia Turkey Ukraine United Arab Emirates Uruguay Venezuela Yemen Yugoslavia Zambia Zimbabwe Ranking » On (no duplicate) Off (allow duplicate) Per-Page » default All Results Timeout » default 1 second 2 seconds 3 seconds 4 seconds 5 seconds 6 seconds 7 seconds 8 seconds 9 seconds 10 seconds 12 seconds 15 seconds 20 seconds Search Bar Download Suggest a Site Personalize MAC MPS III MRKH Machado-Joseph Disease ... Measles, German
Extractions: Match » -All words -Any word -Exact text Search » The Web Jobs / Vacancy Images / Photos FTP / Downloads United Kingdom United States of America Argentina Austria Australia Bangladesh Belgium Bolivia Brazil Bulgaria Canada Chile China Cuba Cyprus Czech Republic Czechoslovakia Denmark Dominican Republic Ecuador Egypt Estonia Finland France Germany Ghana Greece Hong Kong Hungary Iceland India Indonesia Ireland Israel Italy Japan Jordan Kenya Kuwait Latvia Lithuania Luxembourg Malaysia Malta Mexico Moldavia Monaco Morocco Mozambique Nepal Netherlands New Zealand Nicaragua Nigeria North Korea Norway Pakistan Panama Paraguay Peru Philippines Poland Portugal Qatar Romania Russian Federation Saudi Arabia Singapore South Africa South Korea Spain Sri Lanka Sweden Switzerland Taiwan Tanzania Thailand Tunisia Turkey Ukraine United Arab Emirates Uruguay Venezuela Yemen Yugoslavia Zambia Zimbabwe Ranking » On (no duplicate) Off (allow duplicate) Add my Site Toolbar Affiliates MAC MPS III MRKH Machado-Joseph Disease ... Replacements.com - M Manufacturers With Silver Patterns
