Osteomesopyknosis: Difference between revisions

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Latest revision as of 07:56, 4 February 2025

Alternate names[edit]

Axial osteosclerosis

Definition[edit]

Osteomesopyknosis is a bone disorder characterized by abnormal hardening of bone (osteosclerosis).

Cause[edit]

The genetic cause has not yet been identified.

Inheritance[edit]

Autosomal dominant pattern, a 50/50 chance.
  • Osteomesopyknosis is inherited in an autosomal dominant manner.
  • This means that having only one mutated copy of the responsible gene (which has not yet been identified) is enough to cause signs or symptoms of the disorder. When a person with an autosomal dominant condition has children, each child has a 50% (1 in 2) risk to be affected.
  • There have been reported cases where both parents of an affected person did not appear to have the condition.
  • The chance of having signs and symptoms when the responsible mutation is present (penetrance), and potential nature of signs and symptoms (expressivity), is not clear.

Signs and symptoms[edit]

  • Osteomesopyknosis may cause chronic, low-grade back pain in the thoracic (middle) and lumbar (lower) regions.
  • It is considered a mild form of osteosclerosis and is usually found in young adults or teenagers.
  • Height and intellect are not affected.
  • Life expectancy in affected people is normal.
  • There are cases of association with other findings such as ovarian sclerosis and lymphoma; however, it is uncertain whether they have been coincidental or features of the disorder.

Clinical presentation[edit]

For most diseases, symptoms will vary from person to person. People with the same disease may not have all the symptoms listed. 80%-99% of people have these symptoms

  • Increased bone mineral density(Increased bone density)

30%-79% of people have these symptoms

  • Abnormal form of the vertebral bodies
  • Kyphosis(Hunched back)
  • Sclerotic vertebral body
  • Scoliosis

5%-29% of people have these symptoms

  • Abnormal cortical bone morphology
  • Abnormality of metabolism/[[homeostasis](Laboratory abnormality)

Diagnosis[edit]

Treatment[edit]

NIH genetic and rare disease info[edit]

Osteomesopyknosis is a rare disease.


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