Fibrodysplasia Ossificans Progressiva

 

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Definition/Description[edit | edit source]

Fibrodysplasia Ossificans Progressiva is a rare, genetic disorder than transforms ligaments, muscles and tendons into bone outside the skeleton that impairs movement.

Prevalence[edit | edit source]

  • 1 in every 2 million people are diagnosed with Fibrodysplasia Ossificans Porgressiva
  • Nearly 90% of the time it is misdiagnosed and mismanaged. (Lakkrieddy)
  • 67% undergo invasive procedures for diagnosis and treatment
  • More than 50% end up with lifelong disabilities
  • Mostly occurs in children

Characteristics/Clinical Presentation
[edit | edit source]

  • Hearing impairments in approximately 50% of patients
  • Pneumonia and right sided heart failure
  • Controversial malformations
  • Ossification of intercostal muscles
  • Kyphoscoliosis and lordosis
  • Severe weight loss
  • Torticollis
  • TMJ complications

Medications[edit | edit source]

For acute flare-ups:

  • short term high does corticosteroids
  • NSAIDS
  • Biophosphonates


  • Radiotherapy 

Diagnostic Tests/Lab Tests/Lab Values[edit | edit source]

Blood samples

  • Indicate presense of heterozygous R206H mutation of the ACVR1 gene 

Etiology/Causes[edit | edit source]

  • Genetic R206H mutation of the ACVR1 gene
  • ACVR1 gene is a bone morphogenetic protein (BMP) type1 receptor signaling endochondral ossification
  • R206H mutation leads to an increase in enhanced BMP signaling
  • Confirmation of a heterozygous gene mutation of the ACVR1 gene

Systemic Involvement[edit | edit source]

Cardiopulmonary system

  • Lungs affected caused by thoracic insufficiencies
  • Restrictive pulmonary diseases


Nervous system

  • Middle ear ossifications
  • Hearing impairments 

Medical Management (current best evidence)[edit | edit source]

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Physical Therapy Management (current best evidence)[edit | edit source]

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Differential Diagnosis[edit | edit source]

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Case Reports/ Case Studies[edit | edit source]

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Resources
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Recent Related Research (from Pubmed)[edit | edit source]

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References[edit | edit source]

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