Is osteogenesis imperfecta curable ?


Answer:
Osteogenesis imperfecta is a heritable collagen disorder cause diffuse unusual fragility of bone and sometimes accompany by sensorineural audible range loss, blue sclerae, dentinogenesis imperfecta, and communal hypermobility.
There is no specific treatment for Osteogenesis Imperfecta.
Please see the trellis page for more details on Osteogenesis imperfecta.
softly curable.
no !
NOT YET.
Synonyms

* Brittle Bone Disease
* Ekman-Lobstein Disease
* Lobstein Disease (Type I)
* OI
* Vrolik Disease (Type II)

Disorder Subdivisions

* Osteogenesis Imperfecta Type I
* Osteogenesis Imperfecta Type II
* Osteogenesis Imperfecta Type III
* Osteogenesis Imperfecta Type IV

General Discussion

Osteogenesis imperfecta (OI) is a group of bloody disorders affecting the connective tissue and characterized by extremely fragile bones that break or fracture smoothly (brittle bones), repeatedly lacking adjectives lead to. The specific symptoms and physical findings associated near OI come and go greatly from skin to crust. The severity of OI also vary greatly, even among individuals of one and the same family unit. OI may be a mild disorder or may result within severe complications. Four biggest types of OI own be identified. OI type I is the most adjectives and the mildest form of the disorder. OI type II is the most severe. In most cases, the multiple forms of osteogenesis imperfecta are adjectives as autosomal dominant traits.
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Resources

March of Dimes Birth Defects Foundation
1275 Mamaroneck Avenue
White Plains, NY 10605
Tel: (914)428-7100
Fax: (914)997-4763
Tel: (888)663-4637
Email: Askus@marchofdimes.com
Internet: http://www.marchofdimes.com

Osteogenesis Imperfecta Foundation, Inc.
804 West Diamond Avenue
Suite 210
Gaithersburg, MD 20878
USA
Tel: 3019470083
Fax: 3019470456
Tel: 8009812663
Email: bonelink@oif.org
Internet: http://www.oif.org

NIH/National Arthritis and Musculoskeletal and Skin Diseases Information Clearinghouse
1 AMS Circle
Bethesda, MD 20892-3675
USA
Tel: 3014954484
Fax: 3017186366
Tel: 8772264267
TDD: 3015652966
Email: NIAMSinfo@mail.nih.gov
Internet: http://www.niams.nih.gov

Whyte, Michael P., M.D.
Metabolic Research Unit
Shriners' Hospital for Crippled Children
2001 S. Linbergh Blvd.
St. Louis, MO 63131
Tel: (314)532-3600

Canadian Osteogenesis Imperfecta Society
208 Ramona Blvd
Markham
Ontario, L3P 2K8
Canada
Tel: 905-294-5340
Email: rkhayes@ccat.on.ca
Internet: http://www.oif.org

Children's Brittle Bone Foundation
7701 95th St
Pleasant Prairie, WI 53158
Tel: (866)694-2223
Fax: (262)947-0724
Email: info@cbbf.org
Internet: http://www.cbbf.org

NIH/National Institute of Child Health and Human Development
31 Center Dr
Building 31, Room 2A32
MSC2425
Bethesda, MD 20892
Tel: (301)496-5133
Fax: (301)496-7101
Internet: http://www.nih.gov/hichd/

Sjaeldne Diagnoser / Rare Disorders Denmark
Frederiksholms Kanal 2, 3rd Floor
Copenhagen K, 1220
Denmark
Tel: 45 33 14 00 10
Fax: 45 33 14 55 09
Email: mail@sjaeldnediagnoser
Internet: http://www.raredisorders.dk

Let Them Hear Foundation
1900 University Ave #101
East Palo Alto, CA 94303
Tel: (650)462-3143
Fax: (650)462-3143
Tel: (877)735-2929
Email: info@letthemhear.org
Internet: http://www.letthemhear.org

For a Complete Report:

This is an abstract of a report from the National Organization for Rare Disorders, Inc. (R) (NORD). A copy of the complete report can be obtain for a small duty by visit the NORD website. The complete report contains secondary information including symptoms, cause, artificial population, related disorders, standard and investigational treatments (if available), and reference from medical literature. For a full-text journal of this topic, see http://www.rarediseases.org/search/rdbli...

The information provided surrounded by this report is not intended for diagnostic purposes. It is provided for informational purposes solely. NORD recommend that artificial individuals aim the direction or counsel of their own personal physicians.

It is possible that the title of this topic is not the entitle you preferred. Please check the Synonyms fact list to find the alternate name(s) and Disorder Subdivision(s) covered by this report.

This disease entry is base upon medical information available through the date at the closing of the topic. Since NORD's resources are constrained, it is impractical to preserve every entry contained by the Rare Disease Database completely current and accurate. Please check near the agencies planned within the Resources partition for the most current information almost this disorder.

For spare information and assistance just about unusual disorders, please contact the National Organization for Rare Disorders at P.O. Box 1968, Danbury, CT 06813-1968; phone (203) 744-0100; pattern site www.rarediseases.org or email orphan@rarediseases.org

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