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What is Osteogenesis imperfecta, type 2?

What is Osteogenesis imperfecta, type 2?

  • Osteogenesis imperfecta, type 2: A rare lethal form of the genetic connective tissue disorder characterized by fragile bones, blue sclerae and facial and tooth abnormalities.

Osteogenesis imperfecta, type 2: Introduction

Types of Osteogenesis imperfecta, type 2:

Broader types of Osteogenesis imperfecta, type 2:

How serious is Osteogenesis imperfecta, type 2?

Complications of Osteogenesis imperfecta, type 2: see complications of Osteogenesis imperfecta, type 2

What causes Osteogenesis imperfecta, type 2?

Causes of Osteogenesis imperfecta, type 2: see causes of Osteogenesis imperfecta, type 2

What are the symptoms of Osteogenesis imperfecta, type 2?

Symptoms of Osteogenesis imperfecta, type 2: see symptoms of Osteogenesis imperfecta, type 2

Complications of Osteogenesis imperfecta, type 2: see complications of Osteogenesis imperfecta, type 2

Can anyone else get Osteogenesis imperfecta, type 2?

More information: see contagiousness of Osteogenesis imperfecta, type 2
Inheritance: see inheritance of Osteogenesis imperfecta, type 2

Osteogenesis imperfecta, type 2: Testing

Diagnostic testing: see tests for Osteogenesis imperfecta, type 2.

Misdiagnosis: see misdiagnosis and Osteogenesis imperfecta, type 2.

How is it treated?

Doctors and Medical Specialists for Osteogenesis imperfecta, type 2: Medical Geneticist ; see also doctors and medical specialists for Osteogenesis imperfecta, type 2.
Treatments for Osteogenesis imperfecta, type 2: see treatments for Osteogenesis imperfecta, type 2

Name and Aliases of Osteogenesis imperfecta, type 2

Main name of condition: Osteogenesis imperfecta, type 2

Other names or spellings for Osteogenesis imperfecta, type 2:

OI congenital [perinatal, lethal form]

Osteogenesis imperfecta, type 2: Related Conditions

Research the causes of these diseases that are similar to, or related to, Osteogenesis imperfecta, type 2:

  • Rare disorder
  • Heritable disorder
  • Weak bones
  • Collagen syntheisisdwarfism
  • Van der Hoeve's syndrome
 

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