Osteogenesis Imperfecta
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Transcript of Osteogenesis Imperfecta
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Osteogenesis Imperfecta
Dr Osama Farouk Abdulaziz
M.B.B.Ch ,MSc, EBOT
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Osteogenesis Imperfacta
Hereditary condition resulting from a decrease in the amount of normal Type I collagen
Type I collagen ( important for )BoneLigamentsTeethWhite ScleraSkin
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Type I collagen deficiency can result from decreased collagen secretion production of abnormal collagen
Manifest by increase bone fragility low bone mass ( Osteopenia )
Both Autosomal dominant and Autosomal recessive forms
Can be severe or mild (Tarda )
Osteogenesis Imperfecta
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Orthopaedic manifestations Bone fragility and fractures
fractures heal in normal fashion initially but the bone is does not remodelcan lead to progressive bowing
ligamentous laxityShort statureScoliosisCodfish vertebrae (compression fx)
Basilar invagination Olecranon apophyseal avulsion fx
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Non-Orthopaedic manifestations
Blue sclera
Hearing loss less frequent than generally suspected
Dentinogenesis imperfecta brownish opalescent teeth
Wormian skull bones (puzzle piece intrasutural skull bones)
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Symptoms
Mild casesmultiple fractures during childhood
Severe cases present with fractures at birth and can be fatal
Number of fractures typically decreases as patient ages and usually stops after puberty But deformity persist.
Basilar invagination Brain Stem dysfunction apnea, altered consciousness, ataxia, or myelopathyusually in third or fourth decade of life, but can be as early as teenage years
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Physical exam
Multiple fractures leads to
Saber shin appearance of tibia
Bowing of long bones
Scoliosis
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Sillence Classification of Osteogenes Imperfecta (simplified)
Type IMildest form. Presents at preschool age (Tarda).
Autosomal dominant
blue scleraHearing deficit in 50%.
Divided into type A and B based on tooth involvement
Type IIAutosomal recessiveBlue scleraLethal in perinatal period
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Type IIIAutosomal recessive Normal sclereaFractures at birth. Progressively short stature. Most severe survivable form
Type IVAutosomal dominant normal Moderate severity. Bowing bones and vertebral fractures are common.Hearing normal. Divided into type A and B based on tooth involvement
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Type V Hypertrophic callus after fracture. Ossification of IOM ( radius/ulna and tibia/fibula )
Type VI Moderate severity. Similar to type IV
Type VII Associated with rhizomelia and coxa vara
Type V, VI, VII Added to the original classification system .No Type I collagen mutation But have abnormal bone on microscopy and a similar phenotype
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Radiographs
Thin cortices
Generalized osteopenia
Long bone thin and bowed
Pelvis may show acetabular protrusion
Fractures that are at different stages of healing
The vertebra maybe biconcave.
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Diagnosis Diagnosis is based on family history associated
with typical radiographic and clinical features No commercially available diagnostic test( variety of genetic
mutations )
laboratory values are typically within normal range
Possible methods include Fibroblast culturing to analyze type I collagen (positive in 80%
of type IV) can be used for confirmation of diagnosis in equivocal cases
Collagen analysis of a punch biopsyIliac crest biopsy which shows a decrease in cortical widths
and cancellous bone volume, with increased bone remodeling.
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Treatment
Fracture
Bone Deformity
Scoliosis
Prevention
Teratment
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Treatment of Fractures
Fracture prevention
Early bracing Decrease deformity.Stabilize lax joints.Decrease fractures incidence.
Bisphosphonates
Growth hormone Clinical studies showed no increase in bone mass
Bone marrow transplantation
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BisphosphonatesPrevent bone mass loss and decrease bone resorption by suppressing the
activity of osteoclasts. Indications
OsteoporosisMetastatic bone diseaseMultiple myelomaPaget's diseasePolyostotic fibrous dysplasiaTotal joint arthroplasty to prevent osteolysis Early stage avascular necrosis Osteogenesis imperfecta
ContraindicationsSevere renal diseaseLumbar fusion decreased spinal fusion rates Hypersensitivity.Pregnancy.
Side Effects & ComplicationsJaw osteonecrosis Atypical subtrochanteric and femoral stress fractures Radiographic changes consistent with osteopetrosis
Bisphosphonates in O I
Indicated in most cases of OI to reduces fracture rate and pain
Combined with calcium and vitamin D
Increase cortical thickness by inhibiting osteoclasts
Does not affect development of scoliosis
Treatment is less effective after completion of growth.
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Pamidronate Injectable bisphosphonate (Cyclic Intravenous )
Increases cortical bone thickness Increase bone mass and density. Decreases the incidence of fractures. Relieves chronic bone pain. Increases activity levels. Decreases the reliance on mobility
aids. Increases the height of the collapsed vertebral bodies.
BUT
Not decrease the incidence of scoliosis. Zebra lines
Radiographically Pamidronate therapy creates growth lines in the bone
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Bone marrow transplantation Used with some success Introduces normal marrow stem cells that
could potentially differentiate into normal
osteoblasts, Problems of graft rejection and graft versus
host reactions limit this approach.
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Fracture treatment Nonoperative child is less than 2 years
treat as child without OI
OperativeFixation with Telescoping rodes patients > 2 years
allow continued growth
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Treatment of Long Bone Deformities
Realignment Osteotomy with rod fixation (Sofield-Miller procedure)
Indicated in severe deformity to Correct the deformityReduce fracture rates
Techniques include Nontelescopic devicesTelescopic devices
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Treatment of Scoliosis
Observation Curve less than 45 ° Bracing is ineffective
Operativeposterior spinal fusion
Indications for curves > 45 ° in mild forms and > 35 ° in severe forms
TechniqueChallenging due to fragility of bonesUse allograft instead of iliac crest autograftLarge blood loss
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Thank You