Iatrogenic Harm Caused by Diagnostic Errors in Fibrodysplasia Ossificans Progressiva
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چکیده
منابع مشابه
Iatrogenic harm caused by diagnostic errors in fibrodysplasia ossificans progressiva.
BACKGROUND Little is known about diagnostic errors for a disease worldwide. Such errors could alter the disease's natural history, especially if unwarranted interventions cause irreversible harm. Fibrodysplasia ossificans progressiva (FOP), a rare, autosomal dominant genetic disease characterized by episodes of permanent heterotopic ossification of soft tissues, occurs worldwide without racial,...
متن کاملIatrogenic Harm Caused by Diagnostic Errors in Fibrodysplasia Ossificans
Background. Little is known about diagnostic errors for a disease worldwide. Such errors could alter the disease’s natural history, especially if unwarranted interventions cause irreversible harm. Fibrodysplasia ossificans progressiva (FOP), a rare, autosomal dominant genetic disease characterized by episodes of permanent heterotopic ossification of soft tissues, occurs worldwide without racial...
متن کاملFibrodysplasia ossificans progressiva.
Fibrodysplasia ossificans progressiva (FOP) is a rare genetic disorder of the connective tissue characterized by progressive disability as a result of extensive extra skeletal enchondral bone formation and malformed big toes which are often monophalangic. Occasional features include short thumbs, fifth finger clinodactyly, malformed cervical vertebrae and mild mental retardation. Beginning duri...
متن کاملFibrodysplasia ossificans progressiva.
Fibrodysplasia (myositis) ossificans progressiva (FOP) is a rare autosomal dominant disorder in which there is a progressive ectopic ossification and skeletal malformation, mainly in the connective tissue of muscle. The diagnosis is based on the clinical findings and radiological demonstration of the skeletal malformations. We report a 5 year-old female case with FOP.
متن کاملFibrodysplasia Ossificans Progressiva.
Fibrodysplasia Ossificans Progressiva (FOP) is a rare autosomal dominant disorder characterized by postnatal progressive heterotopic ossification of connective tissue and congenital malformation of big toes. We report a 3-year male toddler with clinical and radiological features of FOP. He was born with bilateral hallux valgus and at the age of 3 years presented with hard swellings over back, s...
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ژورنال
عنوان ژورنال: PEDIATRICS
سال: 2005
ISSN: 0031-4005,1098-4275
DOI: 10.1542/peds.2005-0469