81. Initial Standing Of The Osteogenesis Imperfecta Patient - Journal Of Prosthetics Discussed is a design approach to a specific osteogenesis imperfecta case whichwas presented to Children's Hospital at Stanford Rehabilitation Engineering http://www.oandp.org/jpo/library/1990_02_103.asp

Search oandp.org JPO Exact Phrase All Words Any Words Boolean Search Home JPO 1990 Vol. 2, Num. 2 Link to Figures Show Figures Article Text Figures References Send Link Send HTML Article Initial Standing of the Osteogenesis Imperfecta Patient Steve Baum, C.O. Patricia Hazard, C.O. Osteogenesis Imperfecta (O.I.) is more commonly known as "brittle bone disease." The bones are abnormally fragile and will fracture with only minor trauma. Other features of O.I. are weakness, deformity and dwarfism. Bowed long bones and barrel shaped chest are also common. Children of this disease have average to above average intelligence and unimpaired hand function. The primary focus of this paper concerns a specific case presented to Children's Hospital at Stanford. Rehabilitation Engineering Center. At age two, RH., diagnosed with O.I. type III, its most severe form, was presented to us with a prescription for "a total containment orthosis for support in an upright position." At birth R.H. sustained approximately 22 fractures due to his fragile nature, and great care was required to move or position him. R.H. rests almost exclusively supine and has never borne weight on his lower extremities. He can be held in an upright position, non-weight bearing for only a short period of time before complaining of dizziness. The physiologic advantages of being upright in an erect position include improved kidney and bladder drainage, better cardiopulmonary function, and enhanced bone strength from the effects of gravity on the skeletal system.

82. Osteogenesis Imperfecta - English Version osteogenesis imperfecta BRITLE BONE DISEASE. CONTENT. 2. PREVALENCE OFosteogenesis imperfecta. osteogenesis imperfecta is a rare disease. http://ourworld.compuserve.com/homepages/AFBOI/OIenglish.htm

OSTEOGENESIS IMPERFECTA - BRITLE BONE DISEASE CONTENT 1.WHAT IS OSTEOGENESIS IMPERFECTA? 2.PREVALENCE OF OSTEOGENESIS IMPERFECTA 3.WHAT DOES CAUSE OSTEOGENESIS IMPERFECTA? 4.HOW IS OSTEOGENESIS IMPERFECTA DIAGNOSED? ... 10.REFERENCES 1.WHAT IS OSTEOGENESIS IMPERFECTA? Osteogenesis imperfecta: a group of heritable connective tissue disorder Osteogenesis imperfecta (OI) is a heritable connective tissue disorder characterized by defective skeletal matrix which leads to osteopenia with brittle bones and skeletal deformities. This disorder is clinically, biochemically and genetically heterogeneous. Each case of OI is different. These differences are seen in the importance of the brittleness, the slow development, the bone deformations, the presence or the absence of dentinogenesis imperfecta,.... Sillence et al. have classified OI in four groups: * Type I (mild form): - normal or slightly shorter stature - bone fragility without significant deformity - osteopenia - blue sclerae * Type II (lethal form): - intra-uterin death of just after birth caused by rib fractures and difficulties to breath - radiographic examinations possible more or less 15 weeks after fecondation * Type III (severe form): - the more severe viable form - fractures at birth usually seen - hight frequency of fractures - short stature - bone deformities - characteristic triangular face - scoliosis that can lead to bearth difficulties - blue sclerea - barrel-shaped rib cage * Type IV (intermediate form between types I and III) : - relatively short stature - relatively bone deformities - relatively hight frequency of fractures - normal sclerae

83. Bone Disorders - Osteogenesis Imperfecta - Methodist Health Care System, Houston osteogenesis imperfecta What is osteogenesis imperfecta? An estimated 20,00050,000people in the US have this disease. What causes osteogenesis imperfecta? http://www.methodisthealth.com/bone/oi.htm

Bone Disorders Home Page Las Enfermedades de los Huesos (en español) Clinical Services The Methodist Hospital Methodist Diagnostic Hospital Methodist Sugar Land Hospital Methodist Willowbrook Hospital ... Appointment Osteogenesis Imperfecta What is osteogenesis imperfecta? Osteogenesis imperfecta (OI), also known as brittle-bone disease, is a genetic disorder characterized by bones that easily break. There may not be a particular cause for the broken bones. An estimated 20,000-50,000 people in the US have this disease. What causes osteogenesis imperfecta? The cause of OI is believed to be due to a genetic defect that causes imperfectly-formed, or an inadequate amount of, bone collagen a protein found in the connective tissue. What are the types and symptoms of OI? 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 this information from the National Institutes of Health Osteoporosis and Related Bone Diseases National Resource Center, the types and their symptoms include:

84. Osteogenesis Imperfecta osteogenesis imperfecta. Definition. Osteogenesis In osteogenesis imperfecta,the collagen produced is abnormal and disorganized. This http://www.healthatoz.com/healthatoz/Atoz/ency/osteogenesis_imperfecta.html

Encyclopedia Index O Home Encyclopedia Encyclopedia Index O Osteogenesis imperfecta Definition Osteogenesis imperfecta (OI) is a group of genetic diseases of collagen in which the bones are formed improperly, making them fragile and prone to breaking. Description Collagen is a fibrous protein material. It serves as the structural foundation of skin, bone, cartilage, and ligaments. In osteogenesis imperfecta, the collagen produced is abnormal and disorganized. This results in a number of abnormalities throughout the body, the most notable being fragile, easily broken bones. There are four forms of OI, Types I through IV. Of these, Type II is the most severe, and is usually fatal within a short time after birth. Types I, III, and IV have some overlapping and some distinctive symptoms, particularly weak bones. Evidence suggests that OI results from abnormalities in the collagen gene COL1A1 or COL1A2, and possibly abnormalities in other genes. In OI Type I, II, and III, the gene map locus is 17q21.31-q22, 7q22.1, and in OI Type IV, the gene map locus is 17q21.31-q22. In OI, the genetic abnormality causes one of two things to occur. It may direct cells to make an altered collagen protein and the presence of this altered collagen causes OI Type II, III, or IV. Alternately, the dominant altered gene may fail to direct cells to make any collagen protein. Although some collagen is produced by instructions from the normal gene, an overall decrease in the total amount of collagen produced results in OI Type I.

85. The Contact A Family Directory - BRITTLE BONE DISEASES Osteogenesis Imperfecta printer friendly, BRITTLE BONE DISEASES osteogenesis imperfecta, It isconventional to describe four varieties of osteogenesis imperfecta. http://www.cafamily.org.uk/Direct/b27.html

printer friendly BRITTLE BONE DISEASES Osteogenesis Imperfecta home more about us in your area conditions information ... how you can help search this site Brittle Bone Diseases; Osteogenesis Imperfecta (OI) Brittle bone diseases are caused by an abnormality in collagen protein that the body needs for bones as well as other structures such as skin, ligaments and teeth. The condition often leads to an increased likelihood of fractures. Abnormalities in other collagen containing tissues leads to additional problems in some patients such as lax joints, fragile teeth, blue or grey sclera (whites of eyes) and bruising. Some people with OI have short stature and some develop deafness, particularly in the teenage years or their twenties. There are a number of types of brittle bone disease that can vary in severity from mild, in which the patient may not be correctly diagnosed and children may simply be thought to be accident prone, through to severe in which babies have multiple fractures even before birth. The frequency of fractures may increase in adolescence, following childbirth in women and during late adulthood. Fractures need to be treated but the immobilisation period should be kept to a minimum as activity allows muscles and bones to stay as strong as possible. It is important for someone with OI to have a well balanced diet with adequate calcium. There is no specific drug therapy for OI but it has been shown by that a bisphosphonate, pamidronate, can reduce bone loss, the number of fractures and the chronic pain experienced by these children; most children also become more mobile. Most children obtain maximum benefit from this drug over the first two years of treatment. Further research is needed to assess the benefits of treating children with brittle bone disease with this group of drugs. Some children may benefit from insertion of rods to support the bones. Regular monitoring of other functions such as hearing is required.

86. SVOI / ASOI: Osteogenesis Imperfecta In Switzerland Translate this page Die Homepage von SVOI-ASOI befasst sich mit der Behinderung osteogenesis imperfecta(Glasknochenkrankheit), mit primärem Bezug auf Betroffene in der Schweiz. http://www.svoi-asoi.ch/

Homepage SVOI-ASOI Willkommen bei SVOI! Schweizerische Vereinigung Osteogenesis Imperfecta Bienvenue chez ASOI! Association Suisse Osteogenesis Imperfecta Suchen Sie Informationen Vous cherchez des informations Deutschsprachiger Teil unserer Website Kontakt mit SVOI WIEDMER MEDIA ... Contacte avec ASOI

87. Aortic Insuf And Osteogenesis Imperfecta And A New Drug Pamidronate Subject Aortic Insuf and osteogenesis imperfecta and a new Drug Pamidronate TopicArea Congenital Heart Forum The Heart Forum Question Posted By lori on http://www.medhelp.org/forums/cardio/messages/32897a.html

Advertisement Heart Forum Sponsor Developed with The American Heart Association, Med Help and Nexcura encourage you to log on to the FREE Heart Profiler and take advantage of this helpful tool. Med Help International A not-for-profit organization Questions in The Heart Forum are being answered by doctors from The Cleveland Clinic Heart Center , consistently ranked the #1 Heart Center in America. Subject: Aortic Insuf and Osteogenesis Imperfecta and a new Drug Pamidronate Topic Area: Congenital Heart Forum: The Heart Forum Question Posted By: lori on Friday, July 06, 2001 I am a 28 year old female who has Osteogenesis Imperfecta. I have Aortic Regirg Mild to Moderate. I am consisdering starting a drug called PAMIDRONATE in efforts to increase my bond densisty. I was wondering if this drug would impact my heart condition in a negative way.This drug has been around for a while and is used with cancer patients but is showing promise with OI.. Thank you for your assistance. Answer Posted By: CCF-M.D.-CRC on Friday, July 06, 2001

88. ¿QUÉ ES LA OSTEOGENESIS IMPERFECTA? Translate this page Que es la osteogenesis imperfecta? La osteogenesis imperfecta (OI)es una enfermedad cuyo principal problema es la fragilidad ósea. http://www.valentina.8m.net/que es la OI.htm

Free Web site hosting - Freeservers.com Volver a la Portada Signos y Sintomas Tratamientos La atención medica de un niño con OI Lo más importante para un niño con OI ... Tratamiento en Buenos Aires ¿Que es la Osteogenesis Imperfecta? La Osteogenesis Imperfecta (OI) es una enfermedad cuyo principal problema es la fragilidad ósea. En la mayoría de los casos, la enfermedad se genera en forma espontánea pero una vez contraída, puede transmitirse a la descendencia. El hueso normalmente esta formado por la matriz ósea y las fibras de colágeno, constituyendo un tejido y, sobre éste, se depositan los minerales como el calcio y los fosfatos. En la OI, el problema no esta ni en la matriz ósea, ni en el calcio, sino en las fibras de colágeno, que son anormales. La alteración del colágeno es muy variable, puede ser una disminución de la cantidad pero con una estructura normal, o una alteración de la calidad de la fibra. Estas variaciones determinan distintas gravedades de la enfermedad. Si bien los huesos son frágiles, la capacidad de recuperación no está perturbada y las fracturas sueldan muy bien. Comunícate con Nosotros Links Importantes de OI juliosandin@hotmail.com

89. OSTEOGENESIS IMPERFECTA - BOLEST KRHKIH KOSTIJU HRVATSKA UDRUGA osteogenesis imperfecta osteogenesis imperfecta BOLESTKRHKIH KOSTIJU. osteogenesis imperfecta Federation Europe (OIFE). http://smk.mef.hr/osteogenesis/

HRVATSKA UDRUGA OSTEOGENESIS IMPERFECTA OSTEOGENESIS IMPERFECTA BOLEST KRHKIH KOSTIJU Ingeborg Barišiæ : NASLJEÐIVANJE Ingeborg Barišiæ : KLINIÈKA SLIKA ... : MOLEKULARNA PODLOGA OSTEOGENESIS IMPERFECTE PRIRUÈNIK ZA OBOLJELE, NJIHOVE OBITELJI I MEDICINSKO OSOBLJE Osteogenesis Imperfecta Federation Europe (OIFE) Središnja medicinska knjižnica

90. Osteogenesis Imperfecta (Brittle Bone Disease, Lobstein Disease) HOME osteogenesis imperfecta (Congenita) (Brittle Bone Disease, LobsteinDisease). alt IV; osteogenesis imperfecta, TYPE IV; OI4. HOME http://www.bdid.com/oi.htm

HOME Osteogenesis Imperfecta (Congenita) (Brittle Bone Disease, Lobstein Disease) alt.support.osteogenesis.imperfecta OI Osteogenesis Imperfecta (Includes X-Rays) osteogenesis imperfecta OSTEOGENESIS IMPERFECTA (Includes Images) OSTEOGENESIS IMPERFECTA (Includes Images) OI Links Description OSTEOGENESIS IMPERFECTA CONGENITA; OIC The Osteogenesis Imperfecta Foundation ... Case Sixteen - Osteogenesis Imperfecta (Includes X-Rays) Type I osteogenesis imperfecta type I Two pregnancies after preimplantation genetic diagnosis for osteogenesis imperfecta type I and type IV OSTEOGENESIS IMPERFECTA, TYPE I Osteogenesis Imperfecta Type 1: Jojo's Story Type II Osteogenesis imperfecta (Type 2) 15801 Fetus (Includes Photo) OI Type 2 Osteogenesis imperfecta type 2 de Sillence ou Vrolik (Includes Photos and X-Rays) Abnormalities in Central Nervous System Development in Osteogenesis Imperfecta Type II Type III (Progressively Deforming, with Normal Sclerae) OSTEOGENESIS IMPERFECTA, PROGRESSIVELY DEFORMING, WITH NORMAL SCLERAE Type IV Two pregnancies after preimplantation genetic diagnosis for osteogenesis imperfecta type I and type IV OSTEOGENESIS IMPERFECTA, TYPE IV; OI4

91. Osteogenesis Imperfecta osteogenesis imperfecta. Osteogenesis For more information on OsteogenesisImperfecta, contact the following organizations Osteogenesis http://www.clevelandclinic.org/health/health-info/docs/2600/2610.asp?index=9500

92. Loyola University Health System - Bone Disorders - Osteogenesis Imperfecta osteogenesis imperfecta. What is osteogenesis imperfecta? OI can affectmales and females of all races. What causes osteogenesis imperfecta? http://www.luhs.org/health/topics/bone/oi.htm

You are here: Home Health Information Health Topics Bone Disorders Osteogenesis Imperfecta What is osteogenesis imperfecta? 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 cause of OI is believed to be due to a genetic defect that causes imperfectly-formed, or an inadequate amount of, bone collagen a protein found in the connective tissue. What are the types and symptoms of OI?

93. Entrada Do Site OSTEOGÊNESIS imperfecta Site Brasileiro A.B.O.I. Associação Brasileira de Osteogênesis imperfecta Criado e mantido por Rita Amaral 1998 http://www.aguaforte.com/oi

Site Brasileiro A.B.O.I Criado e mantido por Rita Amaral

94. Short Description Of Cell Lines. Pathology: Osteogenesis Imperfecta #166210 Version 4.200205, Short description of cell lines. Pathology osteogenesisimperfecta 166210 OMIM record. By selecting the cell http://www.biotech.ist.unige.it/cldb/pat30.html

Version Short description of cell lines. Pathology: osteogenesis imperfecta OMIM record By selecting the cell line name , you will receive the detailed description of the cell line By selecting one of the terms between parentheses, you will receive the list of all relevant cell lines You can search any term of the list by using the 'Find' utility of your browser human, Caucasian fibroblast GGB human, Caucasian ... By Beatrice...

95. OIFE_TRANSFER *** TRANSFER ***. The OIFE web pages have been moved to our own domain http//www.oife.org/you will be moved there automatically in 10 seconds. http://www.phys.tue.nl/oife/

*** TRANSFER *** The OIFE web pages have been moved to our own domain http://www.oife.org/ you will be moved there automatically in 10 seconds Or you can click here for immediate transfer

96. Deutsche Gesellschaft Für OI Betroffene E.V. Translate this page Die Seite der deutschen OI-Gesellschaft! http://www.oi-gesellschaft.de/

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97. Dfoi.dk http://www.dfoi.dk/

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