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Osteogenesis Imperfecta:     more books (39)

Managing Osteogenesis Imperfecta: A Medical Manual People With Osteogenesis Imperfecta: Michel Petrucciani, Firdaus Kanga, Michael J. Anderson, Atticus Shaffer, Lin Yü-Chih, Nicola Chapman CLINICAL ORTHOPAEDICS AND RELATED RESEARCH NUMBER 159 SEPTEMBER 1981 OSTEOGENESIS IMPERFECTA by J.B. Lipppincott, 1981 The Brittle Bone Syndrome: Osteogenesis Imperfecta by Roger Smith, Martin J. O. Francis, et all 1983-08 What Life Is Like Living with OI: Osteogenesis Imperfecta, Brittle Bones by Patricia Minor, 2006-05-15 IV pamidronate benefits Osteogenesis impertecta. ('Dramatic' Improvement in Bone Pain).: An article from: Pediatric News by Nancy Walsh, 2002-05-01 Mandibular distraction osteogenesis with a small semiburied device in neonates: report of 2 cases.: An article from: Ear, Nose and Throat Journal by Bruno Brevi, Francesco Lagana, et all 2006-02-01 Children with Osteogenesis Imperfecta: Strategies to Enhance Performance Interdisciplinary Treatment Approach for Children with Osteogenesis Imperfecta Osteogenesis Imperfecta: A Guide for Nurses by Osteogenesis Imperfecta Foundation, 2003 Osteogenesis imperfecta: Otologic and maxillofacial aspects (The Laryngoscope) by LaVonne Bergstrom, 1977 Osteogenesis imperfecta The influence of irradiated erosterol and parathyroid extract on the mineral metabolism in osteogenesis imperfecta by Arild Edsten Hansen, 1935 The Official Patient's Sourcebook on Osteogenesis Imperfecta: A Revised and Upda by Icon Health Publications, 2002-01-01

lists with details

21. Osteogenesis Imperfecta Foundation: Fast Facts
    Fast Facts on osteogenesis imperfecta. Definition osteogenesis imperfecta (OI) is a genetic disorder characterized by bones that  
    http://www.oif.org/site/PageServer?pagename=FastFacts

22. MedlinePlus: Osteogenesis Imperfecta
    osteogenesis imperfecta. Printerfriendly version, E-mail this page to a friend. Search MEDLINE for recent research articles on • osteogenesis imperfecta.  
    http://www.nlm.nih.gov/medlineplus/osteogenesisimperfecta.html
    
    Extractions: From the National Institutes of Health Fast Facts on Osteogenesis Imperfecta (Osteoporosis and Related Bone Diseases-National Resource Center) Osteogenesis Imperfecta (Osteoporosis and Related Bone Diseases-National Resource Center) Questions and Answers about Heritable Disorders of Connective Tissue (National Institute of Arthritis and Musculoskeletal and Skin Diseases) General/Overviews Osteogenesis Imperfecta (American Academy of Orthopaedic Surgeons) Anatomy/Physiology Understanding the Structure of Bones (Osteogenesis Imperfecta Foundation) Clinical Trials ClinicalTrials.gov: Osteogenesis Imperfecta

23. MedlinePlus Medical Encyclopedia: Osteogenesis Imperfecta
    osteogenesis imperfecta. Definition Return to top. osteogenesis imperfecta is a congenital (present from birth) condition of abnormal fragility of the bones.  
    http://www.nlm.nih.gov/medlineplus/ency/article/001573.htm
    
    Extractions: @import url(http://www.nlm.nih.gov/medlineplus/images/advanced.css); Skip navigation Other encyclopedia topics: A-Ag Ah-Ap Aq-Az B-Bk ... Z Contents of this page: Pectus excavatum Alternative names Return to top Brittle bone disease Definition Return to top Osteogenesis imperfecta is a congenital (present from birth) condition of abnormal fragility of the bones. Causes, incidence, and risk factors Return to top This bone disorder is usually present at birth as an inherited disease. Osteogenesis imperfecta (OI) is classified into four major types (and further subtypes). All four types of OI are caused by defects in the amount or structure of Type 1 collagen, an important part of the bone matrix. The collagen problem usually results from a dominant genetic defect. This defect may be acquired by several different mechanisms: The defect may be inherited in an autosomal dominant pattern from an affected parent. This means that an affected parent, who carries a single gene for the disorder, has a 50% chance of having children with the disorder. Any child who inherits this gene will be affected. The defect may be acquired by a spontaneous mutation occurring in the individual egg or sperm that formed the child. In this case, neither parent carries a gene for the disorder or is affected by it. The parents, in this case, are no more at risk than the general population for having another child with the disorder.

24. Ms. Dee Dee "B"
    Has a brittle bone disease called, osteogenesis imperfecta. Loves designing webpages, and graphics.  
    http://hometown.aol.com/sweetd484/DD.html

25. NIH ORBD~NRC - Fast Facts On Osteogenesis Imperfecta
    Fast Facts on osteogenesis imperfecta. Definition. Osteogenesis For more information about osteogenesis imperfecta, contact Osteogenesis  
    http://www.osteo.org/newfile.asp?doc=i101i&doctype=HTML Fact Sheet&doctitle=Fast

26. Página En Español Sobre Osteogénesis Imperfecta
    Contiene informaci³n sobre la enfermedad, sus posibles causas, investigaciones relacionadas, y datos del hijo del autor, que sufre la llamada enfermedad de los huesos de cristal .  
    http://osteogenesis.info/
    
    Extractions: imperfecta Qué es la osteogénesis imperfecta Investigación y terapia Organizaciones Foros ... Apadrinar a un niño Bienvenidos Me llamo María Barbero. Mi hijo Pablo tiene osteogénesis imperfecta, una enfermedad congénita bastante rara que afecta a los huesos y a otros tejidos del organismo. Se la suele llamar «la enfermedad de los huesos de cristal», y se abrevia internacionalmente como OI. Se trata de una dolencia con una incidencia relativamente baja entre la población. Los médicos no suelen estar familiarizados con ella; son muy pocos los que tienen experiencia con estos enfermos, y menos aún los que pueden considerarse especialistas. Como ocurre con tantas otras enfermedades, un tratamiento no adecuado puede ocasionar graves perjuicios a los enfermos. Mi intención al preparar mi página es ofrecer a los interesados información general en español sobre la osteogénesis imperfecta y algunos enlaces interesantes (principalmente en inglés) sobre esta enfermedad. No tengo formación médica ni pretendo sentar cátedra con mis opiniones y mis experiencias con la OI. Aunque soy miembro de varias asociaciones de OI, mi página no depende de nadie. Durante los últimos años he ido recopilando información sobre la enfermedad y me gustaría ponerla al alcance de otras familias de afectados, para que no empiecen su búsqueda dando palos de ciego, como yo empecé.

27. Brittle Bone Society - The UK Charity For Osteogenesis Imperfecta
    Gives support to anyone affected by osteogenesis imperfecta, a rare genetic condition which leads to severe and painful fractures.  
    http://www.brittlebone.org/

28. AAOS Online Service Fact Sheet Osteogenesis Imperfecta
    osteogenesis imperfecta. osteogenesis imperfecta (OI) literally means imperfectly formed bones. People with OI have an error (mutation  
    http://orthoinfo.aaos.org/fact/thr_report.cfm?Thread_ID=308&topcategory=About Or

29. OI_mail_list.html
    For the discussion of any issues relating to OI. Open to both professionals and families.  
    http://www.ptialaska.net/~sturm/OI_mail_list.html

30. NFOI
    Norsk Forening for osteogenesis imperfecta The Norwegian osteogenesis imperfecta Foundation.  
    http://home.c2i.net/nfoi/

31. Osteogenesis Imperfecta - About Osteogenesis Imperfecta
    Next . osteogenesis imperfecta. Frederick A. Matsen III, MD. Last updated June 7, 2003 About osteogenesis imperfecta. What is it?  
    http://www.orthop.washington.edu/arthritis/types/osteogenesis/01?close

32. Suomen Osteogenesis Imperfecta -yhdistys R.y.
    Hupsista Selaimesi ei tue kehyksiä! Olisi ehkä syytä hankkia käyttöösi uudempi wwwselain, esimerkiksi viimeisin Internet Explorer.  
    http://www.suomenosteogenesisimperfecta.fi/

33. Osteogenesis Imperfecta / Family Village Library
    Library O P. osteogenesis imperfecta. OI_ADULTS For people who are at least 18 and have osteogenesis imperfecta. Learn More About It.  
    http://www.familyvillage.wisc.edu/lib_oste.htm
    
    Extractions: Web: http://www.oif.org/ The Osteogenesis Imperfecta Foundation is dedicated to helping people cope with the problems associated with OI, by improving the quality of life through education, awareness, mutual support and research into the treatment and potential cure of the disorder. They have local chapters and provide assistance to persons wishing to start a support group in their locality. Additionally, the Foundation provides parent-to-parent matching. The Foundation publishes a quarterly newsletter, Breakthrough , and brochures including, " The Education of a Child with Osteogenesis Imperfecta," in English and Spanish, "The Care of a Baby and Child with Osteogenesis Imperfecta,""OIF General Information," and "I Have OI and Can....".

34. What Is Osteogenesis Imperfecta?
    osteogenesis imperfecta is a genetic disorder characterized by bones that break easily, often from little or no apparent cause.  
    http://allsands.com/Health/Diseases/osteogenesisimp_ryy_gn.htm
    
    Extractions: What is osteogenesis imperfecta? Osteogenesis Imperfecta is a genetic disorder characterized by bones that break easily, often from little or no apparent cause. There are at least four forms of this disorder, ranging in severity. What is OI caused from? bodyOffer(892) OI is caused by a genetic defect that affects the body's production of collagen. Collagen is the major protein of the body's connective tissue. A person who has OI has either not enough collagen or a poor quality of collagen, this leads to weak bones that fracture easily. What are the four types of OI and their characteristics? There are four types of Osteogenesis Imperfecta, they are typed for the severity and charactaristics. Type I: Type one OI is the most common and least severe form of OI. A person with type one would have one or more of the following characteristics: Bones that fracture easily, normal or near normal stature. Loose joints and low muscle tone. Sclera (whites of the eyes) usually have a blue, purple or gray tint. Triangular face, thay have a tendency toward spinal curvature. Bone deformity absent or minimal. Brittle teeth and hearing loss are a possibility. Type II: Type two is the most severe form of OI. Most cases have reported death at birth or shortly after. Numerous fractures and severe bone deformity is normal. Small stature with underdeveloped lungs. Collagen is improperly formed.

35. Osteogenesis Imperfecta
    osteogenesis imperfecta. This baby s extremities are positioned oddly because there have been multiple fractures due to osteogenesis imperfecta (OI).  
    http://medgen.genetics.utah.edu/photographs/pages/osteogenesis_imperfecta.htm
    
    Extractions: This baby's extremities are positioned oddly because there have been multiple fractures due to osteogenesis imperfecta (OI). This disease leads to multiple fractures. The basic problem is a defect in the formation of type 1 collagen that forms bone matrix. There are several types of OI with different inheritance patterns. This is a lethal form of osteogenesis imperfecta (OI) in which the fractures even appear in utero, as revealed by this radiograph of a stillborn fetus. Note the irregular motheaten appearance of the long bones of the arm. Examinations Photographs Movies Links ... noJava Home

36. Osteogenesis Imperfecta Study
    New Hope for Children with osteogenesis imperfecta. The Shriners Hospital for Children in Tampa is participating in a multicenter  
    http://www.shrinershq.org/shc/tampa/news/02/oistudy.html
    
    Extractions: Donate to Shriners Hospitals for Children online Back to Tampa Shriners Hospital The Shriners Hospital for Children in Tampa is participating in a multicenter research study to evaluate the oral drug, alendronate as a possible medical treatment for children with severe Osteogenesis Imperfecta (OI). Alendronate is a drug currently approved by the FDA for use in the treatment of osteoporosis. We wish to determine if taking alendronate for two years will result in thicker, stronger bones, reduce skeletal pain, improve how well patients get about and reduce fracture rates in children with OI. Osteogenesis Imperfecta can literally be translated as "imperfectly formed bones." Most forms of OI are caused by imperfectly formed bone collagen that results from a genetic defect. It is believed that there are between 20, 000 and 40, 000 people with OI in the United States. Patients age 4-18 years who are eligible to participate in this study include type III or IV OI and type I OI with either: chronic pain, 3 or more fractures per year for the previous 2 years, or limb deformity requiring surgical correction. To find out more about this alendronate research study at the Shriners Hospital for Children in Tampa, please contact the Clinical Research Associate, Nancy Pisciotto, RN, ONC at 813-975-7130, or email

37. Osteogenesis Imperfecta-Bone Diseases And Disorders
    Bone Diseases. osteogenesis imperfecta. What is osteogenesis imperfecta? OI can affect males and females of all races. What causes osteogenesis imperfecta?  
    http://www.umm.edu/bone/oi.htm
    
    Extractions: Osteogenesis imperfecta (OI), also known as brittle-bone disease, is a genetic (inherited) disorder characterized by bones that break easily without a specific cause. An estimated 20,000 to 50,000 people in the US have this disease. The disorder occurs in one out of 20,000 to one out of 60,000 live births. OI can affect males and females of all races. What causes osteogenesis imperfecta? The following are the most common symptoms for osteogenesis imperfecta. However, each individual may experience symptoms differently. Although symptoms may vary, generally they are used to classify the four forms of OI, each of which represents the severity of the condition. According to the Osteoporosis and Related Bone Diseases National Resource Center, part of the National Institutes of Health (NIH), the types of OI and their symptoms include the following:

38. Pedersen Family Home Page & Osteogenesis Imperfecta
    Pedersen Family Home Page, Our home page is a bit about us but mostly about our daughter Danilee who has osteogenesis imperfecta or as it is more commonly  
    http://www3.bc.sympatico.ca/orp/main.html

39. Osteogenesis Imperfecta
    Beginpagina — Ziekten en aandoeningen — osteogenesis imperfecta (OI) osteogenesis imperfecta (OI) Korte beschrijving Osteogenesis  
    http://www.erfocentrum.nl/zena/osteo.php
    
    Extractions: Osteogenesis imperfecta (OI) is een zeldzame aangeboren aandoening van het steungevende weefsel. Daartoe behoren ondermeer botten, tandbeen, gewrichtskapsels en het steunweefsel van de huid. Door de afwijkende bouw zijn deze weefsels minder stevig: botten kunnen bijvoorbeeld makkelijk breken of kromgroeien. Ook kunnen andere verschijnselen voorkomen zoals blauw oogwit, doofheid, achterblijven in groei, abnormaal beweeglijke gewrichten en afwijkingen aan het gebit. Diagnose

40. Osteogenesis Imperfecta
    osteogenesis imperfecta. osteogenesis imperfecta is divided into the type which is diagnosed at birth (congenita) and the type that is diagnosed later (tarda).  
    http://www.dbpeds.org/conditions/conditions.cfm?Abbrev=osteogenesis_imperfecta

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