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         Neurofibromatosis:     more books (99)
  1. Cafe Au Lait Spots May Signal Neurofibromatosis.(Brief Article): An article from: Family Practice News by Nancy Walsh, 2001-03-15
  2. Neurofibromatosis: a young woman's journey--case study.(Case study): An article from: Journal of Neuroscience Nursing by Susan Milliken, 2007-12-01
  3. Tuberous Sclerosis and Neurofibromatosis: Epidemiology, Pathophysiology, Biology, and Management : Proceedings of the International Symposium on Neu (Japan ... Foundation Publishing Series, No. 28) by International Symposium on Neurocutaneous Syndrome, Yasumasa Ishibashi, et all 1990-12
  4. Understanding neurofibromatosis: An introduction for patients and parents by James H Tonsgard, 1993
  5. Neurofibromatosis: January 1984 through June 1987, 720 citations (Literature search) by Jacqueline Van de Kamp, 1987
  6. Joint Resolution Designating November 1992 as "Neurofibromatosis Awareness Month." (SuDoc AE 2.110:102-577) by U.S. National Archives and Records Administration, 1992
  7. Neurofibromatosis Type I: From Genotype to Phenotype (A Volume in the Human Molecular Genetics Series) (Human Molecular Genetics) by M. Upadhyaya, 1980
  8. Descriptive analysis of tibial pseudarthrosis in patients with neurofibromatosis 1 (The James A. Bush memorial research awards) by D. A Stevenson, 1997
  9. Descriptive analysis of tibal pseudarthrosis in patients with neurofibromatosis 1 (The James A. Bush Memorial Research Awards) by David A Stevenson, 1997
  10. Neurofibromatosis (Current problems in surgery) by John V Wander, 1977
  11. Fibroma molluscum, or universal neurofibromatosis by A Ravogli, 1911
  12. Neurofibromatosis (v. Recklinghausen's disease): A clinical -psychiatric and genetic study by Birgitta Samuelsson, 1981
  13. Type 1 neurofibromatosis and the pediatric patient (Current problems in pediatrics) by Vincent M Riccardi, 1992
  14. Las neurofibromatosis (SuDoc HE 20.3520:N 39/SPAN.) by U.S. Dept of Health and Human Services, 2000

61. The Contact A Family Directory - NEUROFIBROMATOSIS
printer friendly, neurofibromatosis, Internet article. THE neurofibromatosisASSOCIATION. The neurofibromatosis Association 82 London
http://www.cafamily.org.uk/Direct/n27.html
printer friendly NEUROFIBROMATOSIS home more about us in your area conditions information ... how you can help search this site Neurofibromatosis (Nf) is an inherited genetic disorder causing tumours on nerve tissue anywhere in the body and often other effects. There are two main types of neurofibromatosis: Nf1 caused by a defect on Chromosome 17 (90% of cases) and Nf2 caused by a defect on Chromosome 22. Major features of Nf2 include bilateral acoustic neuromas (Vestibular schwannomas) which usually begin to cause problems in the late teens or early twenties although rarely some are later onset. Minor features of Nf2 include juvenile lenticular cataracts and possibly CAL spots (but fewer than in Nf1). Complications of Nf2 include brain tumours which are normally benign - the most common type being meningiomas, spinal tumours and skin tumours - Schwannomas which may be similar to neurofibromas in Nf1. Inheritance patterns
Autosomal dominant. 50% of cases result from spontaneous new mutations in families with no previous history of the disorder. Pre-natal diagnosis
Possible in both Nf1 and Nf2. Severity of effect cannot be predicted in Nf1 but can sometimes be predicted in Nf2. Brain scans or genetic studies may allow early diagnosis or presymptomatic diagnosis in Nf2.

62. Health Information Resource Database: Neurofibromatosis, Inc.
neurofibromatosis, Inc. Contact Information. John Vickerman 8855 AnnapolisRoad Suite 110 Lanham, MD 207062924. neurofibromatosis, Inc.
http://www.health.gov/NHIC/NHICScripts/Entry.cfm?HRCode=HR2436

63. Health Information Resource Database: National Neurofibromatosis Foundation
Services.. National neurofibromatosis Foundation. Contact Information.Casandra Gomez 95 Pine Street 16th Floor New York, NY 10005.
http://www.health.gov/NHIC/NHICScripts/Entry.cfm?HRCode=HR0271

64. Neurofibromatosis
Translate this page neurofibromatosis. Esta página se ha movido. Oprima aquí para verla información más actualizada sobre este tema. ©2002 March
http://www.nacersano.org/BibliotecaDeSalud/informatiuas/neurofibromatosis.htm
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Neurofibromatosis
Esta página se ha movido. Oprima aquí para ver la información más actualizada sobre este tema. ©2002 March of Dimes Birth Defects Foundation. Todos los derechos reservados.

65. Neurofibromatosis NETWORK, Von Recklinghausen, NF, NF1, NF2
Although it is maintained by this association it is in no way subject to itnor is it dependent on any other association. neurofibromatosis Webring.
http://www.neurofibromatosis-network.org/
NF NET ORK European Ass European Contacts NF World Links Personal Websites ... Page d'accueil IMPORTANT NOTICE -The European Year of People with Disabilities... EUROP E AN NEUROFIBR OM ATOSIS ASSOC I ATIONS PARTNERS SOLIDARITY Together we can: T rust, O vercome, G row, E ncourage, T eam up, H ope, E stablish, R eassure SOLIDARITY C reat ion in N umber of visitors - Last modified Contact us No request for medical help will be posted on this site and the webmanager is not responsible for anyone linked to this site who does offer such help. This site is maintained and designed by Ms L. Clare Savoca, president of the 'Groupe d'entraide romand - NF', a Swiss Romande association for the French speaking part of Switzerland. Although it is maintained by this association it is in no way subject to it nor is it dependent on any other association.
This Neurofibromatosis Webring
owned by NF NETWORK
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66. Neurofibromatosis
Professionals only. neurofibromatosis,, Print this article, an Fora general description, see neurofibromatosis. Eight subtypes of
http://www.amershamhealth.com/medcyclopaedia/Volume III 1/neurofibromatosis.html
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*For Medical Professionals only, registration required Neurofibromatosis, an autosomal dominant disorder involving multiple systems, which is characterized by a clinical triad of cutaneous lesions, mental deficiency and skeletal deformities. For a general description, see neurofibromatosis Eight subtypes of the disease have been identified, although only two subtypes (neurofibromatosis-1 and neurofibromatosis-2) account for 99% of cases. Neurofibromatosis-1 is also known as von Recklinghausen's disease. Cafè au lait spots and the lesions of molluscum fibrosum are common. Another typical manifestation is a lesion of the iris termed the Lisch nodule . These nodules may be neurofibromas arising from peripheral schwannian elements or melanocytic hamartomas of neural crest origin. Bone abnormalities involve the cranium, spine and other sites.

67. Neurofibromatosis
neurofibromatosis,, Print this article, a group of heterogeneous conditions.According to the National Institutes of Health (NIH) only
http://www.amershamhealth.com/medcyclopaedia/Volume VI 1/neurofibromatosis.html
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*For Medical Professionals only, registration required Neurofibromatosis, a group of heterogeneous conditions. According to the National Institutes of Health (NIH) only two types of neurofibromatosis are defined: neurofibromatosis type 1 (NF1) also called von Recklinghausen's disease; and neurofibromatosis type 2 (NF2) or bilateral eighth nerve schwannomas syndrome. The definition of "peripheral" and "central" neurofibromatosis, referred in the past to NF1 and NF2, respectively, has now been abandoned since the two conditions often have central and peripheral manifestations together. Neurofibromatosis Type 1 (NF1) NF1 is an autosomal dominant disorder with high penetrance but variable expressivity. The gene responsible is on the long arm of chromosome 17 and normally acts as a tumour-suppressor oncogene. The lack of both copies of the gene induces the growth of a variety of neoplasms and non-neoplastic lesions. The major target organs are both peripheral (PNS) and central (CNS) nervous system and the skin, but virtually widespread multiple organ system involvement occurs. NF1 is far more common than NF2 and affects approximately 1 in every 2,000–3,000 births.

68. Neurofibromatosis
neurofibromatosis. Case 50year-old female. The patient had a tumorousmass at the right hard palate for 20 years. The mass is asymptomatic.
http://w3.dh.nagasaki-u.ac.jp/cgi-bin/t_file2?code=JOG

69. Eye Conditions > Neurofibromatosis -- EyeMDLink.com
Last Updated 10/21/2001. neurofibromatosis. neurofibromatosis is an inheriteddisorder characterized by the growth of tumors known as hamartomas.
http://www.eyemdlink.com/Condition.asp?ConditionID=299

70. Neurofibromatosis
neurofibromatosis. neurofibromatosis Resources. NF Network. The National neurofibromatosisFoundationneurofibromatosis Clinics Association, Inc. new.
http://theresourcesite.com/disabilityresources/neurofibromatosis.htm
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Neurofibromatosis Resources NF Network The National Neurofibromatosis Foundation Neurofibromatosis Clinics Association, Inc. new The Neurofibromatosis Association UK new Neurofibromatosis, Inc Neurofibromatoses. fact sheet from the March of Dimes new The Neurofibromatoses new feedback link to The Resource Site

71. HealthlinkUSA Neurofibromatosis Links
medical and health related topics. FindWhat. Click here for page 1 ofneurofibromatosis information from the HealthlinkUSA directory.
http://www.healthlinkusa.com/223ent.htm

72. Neurofibromatosis
neurofibromatosis type I, or von Recklinghausen disease, is a autosomal dominantdisorder affecting the mesodermal and neuroectodermal tissues.
http://www.stevensorenson.com/residents6/neurofibromatosis.htm

Home
Up [ Neurofibromatosis ] Pyknodysostosis Mucopolysaccharidoses Multiple hereditary exostoses Ollier disease ... Dyschondrosteoses Neurofibromatosis type I, or von Recklinghausen disease, is a autosomal dominant disorder affecting the mesodermal and neuroectodermal tissues. Fifty percent of cases are due to spontaneous mutations. The incidence is 1 in 2,000 to 4,000 births. This is most common phakomatosis. Clinically, neurofibromas, cafe au lait spots, axillary/inguinal freckling, Lisch nodules (iris hamartomas), and osseous lesions are observed. A sharp angled scoliosis is characteristic of the disease, causing dwarfism. On occasion, the disease may produce a shortened limb due to bowing and pseudarthrosis, focal gigantism is more common, due to overgrowth of an ossification center, causing marked enlargement of a digit in the hand or foot. Treatment consists of scoliosis management. Usually, the scoliosis is refractory to bracing, and fusion may be required. REFERENCES Liebermann F, Korf BR. Emerging approaches toward the treatment of neurofibromatoses. Genet Med. 1999 May-Jun;1(4):158-64; quiz 165-6. Parada LF. Neurofibromatosis type 1. Biochim Biophys Acta. 2000 Jul 31;1471(1):M13-9.

73. Online Dermatology Image Library
Dermatlas Dermatology neurofibromatosis,neurofibroma,neurofibroma,neurofibroma,neurofibroma,freckles,dermatologyimage,café au lait spot, plexiform
http://dermatlas.med.jhmi.edu/derm/result.cfm?Diagnosis=83

74. Expert Advice -- Neurofibromatosis
neurofibromatosis Could you tell me about neurofibromatosis. neurofibromatosis (NF)is a inherited genetic disorder which causes typical skin and nerve tumors.
http://www.parentsoup.com/experts/ped/qas/0,,200533_417046,00.html
var cimsCid = ''; var cimsUid = '417046';
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TOPICS Activities and fun Ages and stages Behavior problems Child health ... Parenting A-Z FEATURES Boards Chats Debates Experts ... Workshops FREE NEWSLETTERS Parent Soup ParentsPlace more newsletters Neurofibromatosis Could you tell me about neurofibromatosis. My daughter has NF1 in her brain, back, and right foot. Robert Steele, M.D.

75. Neurofibromatosis
neurofibromatosis. neurofibromatosis is well known and was first feltto be occurring in James Merrick, or the elephant man . Today
http://www.worldcf.org/neurofibro.html
World Craniofacial Foundation
7777 Forest Lane, Ste C-621
P.O. Box 515838
Dallas, TX 75251-5838
fax 972-566-3850
worldcf@worldnet.att.net
Neurofibromatosis Neurofibromatosis is well known and was first felt to be occurring in James Merrick, or the "elephant man". Today we know that his diagnosis was Proteus syndrome. The cause of neurofibromatosis, or von Recklinghausen disease, is unknown but there is a genetic predisposition. The characteristics present in an infant with simple cafe au lait spots and minimal deformity. In time, this may progress into more massive deformities. Three basic types exists. Plexiform neurofibroma are flat lesions of moderate size which tend to follow the the nerve or nerve axis with marked enlargement. It infiltrates through the skin, subcutaneous tissue, deep planes, and even cause distortion of growth of the bone. Mollusca fibrosa are small round nodules which may be present in large numbers. Elephantiasis neurofibromatosa is the most impressive manifestation due to its size. In this setting the lesion will lead to massive overgrowth of both the skin and the associated soft tissue. Frequent, repeated surgical excision is performed and can give improvement. But since infiltration is throughout all of the planes of the tissues involved, it can be a long term progressive problem.

76. Neurofibromatosis
neurofibromatosis, research index site with links for disability users, 1000'sof search engines and with live java games, chat's, kids internet, irc, jobs
http://www.ability.org.uk/neurofib.html
Our Aims Services Stats ... Z Neurofibromatosis National Neurofibromatosis Foundation - info about neurofibromatosis and the Foundation. Webmaster . Site Design by Ability "see the ability, not the disability" Acknowledgments

77. © The Centre For Genetics Education
Fact Sheet 26, Last Updated May 2002. neurofibromatosis. Producedby the Centre for Genetics Education. WHAT IS neurofibromatosis?
http://www.genetics.com.au/Genetics2003/FactSheets/26.asp
GENETIC FACT SHEETS
Fact Sheet 26 Last Updated: May 2002 NEUROFIBROMATOSIS Produced by the Centre for Genetics Education. Fax: (02) 9906 7529 Email: genetics@med.usyd.edu.au Internet: www.genetics.com.au
Adobe Acrobat PDF Printable Version (14 KB)
WHAT IS NEUROFIBROMATOSIS?
Neurofibromatosis (NF) is a disorder in which benign (noncancerous) "lumps" or tumours develop in the tissue of the body's nervous system. The tumours, called neurofibromas, grow in, and also around, nerves in various parts of the body, particularly the skin.
NF affects both sexes equally and is found in all nationalities. It affects about 1 person in every 3,000 throughout the world. Doctors have identified several different types of neurofibromatosis.
WHAT ARE THE DIFFERENT TYPES OF NEUROFIBROMATOSIS?
There are two main types of NF: type 1 and type 2. The main characteristics of the two types are described below.
1. Neurofibromatosis type 1
Neurofibromatosis type 1 (NF1) is the most common type, affecting about 90% of those people with NF. It was first described by a German doctor named Frederich von Recklinghausen in 1882 and thus the condition is also known as Von Recklinghausen's disease.
People affected with NF1 vary greatly in the expression of the symptoms. Some are mildly affected, having only one or two of the symptoms while others, even in the same family, are more severely affected. Regular medical review is recommended for children with NF1.

78. NIH Guide: NEUROFIBROMATOSIS
neurofibromatosis NIH GUIDE, Volume 21, Number 9, March 6, 1992 PA NUMBER PA92-47PT 34 Keywords AIDS Biology, Cellular Molecular Genetics Pathophysiology
http://grants.nih.gov/grants/guide/pa-files/PA-92-047.html
Return to 1992 Index Return to NIH Guide Main Index
Department of Health
and Human Services
National Institutes of Health (NIH)
9000 Rockville Pike
Bethesda, Maryland 20892

79. Neurofibromatosis Type 1
CASE STUDY No. 10. neurofibromatosis Type 1. At the time of Why doesour child have neurofibromatosis? neurofibromatosis is one of
http://www.intouchlive.com/cancergenetics/nf1.htm
CASE STUDY No. 10
Neurofibromatosis Type 1
At the time of his birth, BG was noted to have large brown spots over his abdomen and upper thighs. In the nursery, the pediatrician raises with the parents the possibility that their child may have neurofibromatosis type 1. Before any formal genetic counseling, they quickly go to their nearby library, and using a series of medical reference books, learn to their horror that neurofibromatosis type 1 is a serious, disfiguring genetic disorder associated with a propensity to develop various forms of life-threatening cancers. Attending a multidisciplinary clinic that evaluates children and adults for neurofibromatosis, the staff, including a medical geneticist and a dermatologist, reaffirm their pediatrician's initial concern and attempt to provide detailed medical information to the parents about the potential clinical effects of neurofibromatosis type 1. The parents are informed that neurofibromatosis type 1 is a genetic disorder characterized by:
  • café-au-lait (coffee-with-cream colored) spots of the skin (six or more spots exceeding 5 mm in diameter are considered diagnostic);

80. Neurofibromatosis, NF1, NF2, Support
Translate this page A resource for those who have neurofibromatosis to communicate with eachother using the internet. neurofibromatosis, NF1, NF2, Support.
http://home.sunrise.ch/burch
Main Topics:

Page construction: 26 May 1996
Last update: June 21, 1999
What's new since April 1:
Purpose: A resource for those who have Neurofibromatosis to communicate with each other using the internet. Also, parents of affected children may find or give support.
Translation:
  • Bjorn is willing to translate Italian - English. Sono disposto a tradurre gratuitamente dall'inglese per coloro che cercano informazioni sulle Neurofibromatosi nell'Internet.
  • The Webmaster is willing to translate information regarding NF on this home page. English, Dutch, German, Swiss-German and French.

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