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Osteogenesis Imperfecta

Osteogenesis imperfecta (OI), commonly known as brittle bone disease, is a group of genetic bone disorders. People with OI either have less collagen than normal or the quality is poorer than normal. As collagen is an important protein in bone structure this impairment causes those with the condition to have weak or fragile bones. more...

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As a genetic disorder, OI is a autosomal dominant defect. Most people with OI receive it from a parent but it can also be an individual (de novo or "sporadic") mutation.

Types

There are four types of OI, though the symptoms range from person to person. Type I is the most common and mildest form, followed by Type IV, Type III and Type II. A Type V has been proposed based on studies of Type IV.

Type I

  • OMIM 166200 - Type I
  • OMIM 166240 - Type IA

Collagen is normal but not of a high enough quantity:

  • Bones fracture easily, especially before puberty
  • Slight spinal curvature
  • Loose joints
  • Poor muscle tone
  • Discolouration of the sclera (whites of the eyes)
  • Early loss of hearing

Type II

  • OMIM 166210 - Type II

Collagen is not of a sufficient quality or quantity

  • Most cases die before adulthood
  • Severe respiratory problems due to underdeveloped lungs
  • Severe bone deformity and small stature

Type III

  • OMIM 259420 - Type III

Collagen quantity is sufficient but is not of a high enough quality

  • Bones fracture easily, sometimes even before birth
  • Bone deformity, often severe
  • Respiratory problems possible
  • Short stature, spinal curvature and barrel-shaped rib cage
  • Loose joints
  • Poor muscle tone in arms and legs
  • Discolouration of the sclera (whites of the eyes)
  • Early loss of hearing

Type IV

  • OMIM 166220 - Type IV

Collagen quantity is sufficient but is not of a high enough quality

  • Bones fracture easily, especially before puberty
  • Short stature, spinal curvature and barrel-shaped rib cage
  • Bone deformity is mild to moderate
  • Discolouration of the sclera (whites of the eyes)
  • Early loss of hearing

Treatment

At present there is no cure for OI so treatment is aimed at maintaining mobility and strengthening bones as much as possible.

Physiotherapy is used to strengthen muscles and improve motility in a gentle manner which minimises bone breakages. This often involves hydrotherapy and the use of support cushions to improve posture. Individuals are encouraged to change positions regularly throughout the day in order to balance the muscles which are being used and the bones which are under pressure. One of the biggest problems is that children often develop a fear of trying new ways of moving due to movement being associated with pain. This can make physiotherapy difficult to administer to young children.

Read more at Wikipedia.org


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C-Section Has No Impact on Fracture Risk in Infants With Osteogenesis Imperfecta
From OB/GYN News, 12/15/99 by Barbara Baker

SAN FRANCISCO -- Cesarean section does not reduce the fracture risk of infants with osteogenesis imperfecta, investigators found in a retrospective review.

Nor does an operative delivery improve survival among those with severe disease, Dr. Peter H. Byers said at the annual meeting of the American Society of Human Genetics.

"The major indication for cesarean section of infants with osteogenesis imperfecta [OI] is therefore obstetric, not genetic," said Dr. Byers of the University of Washington, Seattle.

OI is a genetic collagen disorder caused by defective biosynthesis of type I collagen. It's associated with easily fractured bones and can range in severity from mild disease to a type that causes death in the perinatal period.

To determine whether mode of delivery influences outcome, Dr. Byers and his associates reviewed data on 167 women who delivered infants with OI. The diagnosis of OI was made prenatally in 39 women, almost all by ultrasound.

Ninety of the infants were delivered by cesarean section. The reason for an operative delivery was suspected OI in only 14 cases. Forty-eight were delivered operatively because of a nonvertex presentation and the rest because of other obstetrical indications.

Forty-four of 120 (37%) infants delivered at term had a breech presentation. The frequency of a breech presentation at term in the general population is 4%.

The percentage of neonates with new fractures diagnosed at birth did not vary by mode of delivery for all types of OI. Among infants with type I, the mildest form of OI, 2 of the 13 infants delivered by cesarean section and 4 of 16 delivered vaginally had new fractures. Similar patterns were seen for those with intermediate-severity disease, types III and IV.

All 50 infants with type II OI, the lethal type of disease, had dozens of new fractures, regardless of the mode of delivery.

Infants with type II disease delivered by cesarean section were more likely to be alive at 1-3 days of life than those delivered vaginally, but mode of delivery had no impact on survival by 2 weeks of life. All infants in this group died, Dr. Edith Cheng, also of the university, said in an interview.

COPYRIGHT 1999 International Medical News Group
COPYRIGHT 2004 Gale Group

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