Osteosarcoma occurring in osteogenesis imperfecta tarda
نویسندگان
چکیده
منابع مشابه
Osteogenesis imperfecta tarda (a case report).
The case of type IA of osteogenesis imperfecta tarda was described. Following results were presented: anamnesy, physical, ophthalmic and ORL examinations, laboratory findings, radiological and densitometric data. Clinical characteristic and mentioned above examinations allowed to take the definitive diagnosis. Family data showed features of this disease in the next generations and should be a b...
متن کاملOsteogenesis imperfecta tarda treated with sodium fluoride.
Osteogenesis imperfecta is a disorder of connective tissue, existing in a severe form (congenita) and a milder form (tarda) both being inherited as an autosomal dominant (McKusick, 1966). Recently Aeschlimann, Grunt, and Crigler (1966) and Bilginturan and Ozsoylu (1966) reported three infants with osteogenesis imperfecta congenita who improved, as regards survival and frequency of spontaneous f...
متن کاملOsteogenesis Imperfecta Tarda. A Review with Case Reports
S. |NIYOGI, m.b. (Cal.) Surgical Registrar,"Nilratan Sarkar Medical College Hospitals, Calcutta Osteogenesis imperfecta tarda is one variety a clinical syndrome which has been given various names such as fragilitas ossium, idiopathic osteopsathyrosis, periosteal dysplasia, etc. Thomson (1921) divided it into two broad clinical types?preand post-natal. Pre-natal cases are more severe and often t...
متن کاملOsteogenesis imperfecta
Keywords Disease name and synonyms Definition/Diagnosis criteria Differential diagnosis Frequency Clinical description Etiology Diagnostic methods Management Treatment Genetic counselling References Abstract Osteogenesis imperfecta (OI) is a group of inherited diseases responsible for varying degrees of skeletal fragility. Minimal trauma is sufficient to cause fractures and bone deformities. A ...
متن کاملOsteogenesis imperfecta.
Our clinical files on osteogenesis imperfecta are brought up-to-date reviewing a total of 33,555 cases admitted between 4/XII/48 and 31/VIII/76. From these, 5 clinical cases were found. The extreme rareness of this regional pathology in our Cátedra y Sericio de Pediatría, which is the largest concentration center in Paraguay had led us to make this publication. From our casuistics, we may singl...
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ژورنال
عنوان ژورنال: International Orthopaedics
سال: 2002
ISSN: 0341-2695,1432-5195
DOI: 10.1007/s00264-001-0323-3