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Fibrodysplasia ossificans progressiva
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نویسنده
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bari a. ,jabeen u. ,zeeshan f. ,iftikhar a. ,ahmad s. ,rathore a.w.
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منبع
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pakistan paediatric journal - 2015 - دوره : 39 - شماره : 2 - صفحه:118 -121
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چکیده
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Fibrodysplasia ossificans progressiva (fop) is a rare inherited autosomal dominant disorder characterized by congenital malformation of the big toes and progressive heterotopic ossification of the connective tissue. we report a four-year-old boy who had clinical features and radiological findings suggestive of fop. he presented with significant decreased range of neck movement and a painful swelling in the upper paraspinal region. his radiographs showed halux valgus along with heterotopic ossification in the neck and thoracic region. © 2015,pakistan pediatric journal. all rights reserved.
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کلیدواژه
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FOP; Heterotopic ossification
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آدرس
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department of pediatric medicine,the children’s hospital,institute of child health,lahore, Pakistan, department of pediatric medicine,the children’s hospital,institute of child health,lahore, Pakistan, department of pediatric medicine,the children’s hospital,institute of child health,lahore, Pakistan, department of pediatric medicine,the children’s hospital,institute of child health,lahore, Pakistan, department of radiology,shaikh zayed hospital,lahore, Pakistan, department of pediatric medicine,the children’s hospital,institute of child health,lahore, Pakistan
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Authors
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