osteogenesis imperfecta in pregnancy: case report
نویسندگان
چکیده
osteogenesis imperfecta is a rare inherited connective tissue disorder with an expression that varies from mild to severe disease affecting bone, sclera and middle ear. fertility is preserved, especially in those patients with type 1. we present hereby a pregnant woman with osteogenesis imperfecta that had over 30 fractures in long bones and vertebrae. the object of this report was to determine choice of delivery method, maternal and neonatal complications and prenatal diagnosis.
منابع مشابه
Osteogenesis imperfecta in pregnancy. Case report.
BACKGROUND AND OBJECTIVES Osteogenesis Imperfecta is a rare condition, especially in obstetric patients. It has an estimated prevalence of 1/10,000 in the general population, and 1/25,000 to 30,000 in obstetric patients. The objective of this report was to present a rare case of a pregnant woman with Osteogenesis Imperfecta undergoing cesarean section. CASE REPORT This is a 23 years old gravi...
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Paraplegia occurred in an adolescent girl with osteogenesis imperfecta after chiropractic manipulation. The child had been able to walk freely out of doors. Complete motor paralysis with sensory sparing resulted due to anterior compression of the cord by spondyloptotic cervical vertebrae. Reconstructed computerised tomography was very helpful in demonstrating the abnormality. Anterior and then ...
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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...
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A 15-year-old male patient was admitted to hospital having experienced repeated fractures over the previous three years, predominantly due to falling down or overexertion. The clinical signs and radiological features, such as recurrent fractures, blue sclera and low bone mineral density (BMD) level, all led to the diagnosis of a mild form of osteogenesis imperfecta (OI) type I. The patient bega...
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BACKGROUND AND OBJECTIVES Osteogenesis Imperfecta is an uncommon genetic connective tissue disease with prevalence of 1/10000, primarily involving endochondral ossification, resulting in brittle bones, multiple fractures and skeletal deformities. This article aimed at reporting a case of Osteogenesis Imperfecta patient submitted to total intravenous anesthesia for fractured femur surgical repai...
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عنوان ژورنال:
journal of family and reproductive healthجلد ۵، شماره ۱، صفحات ۳۱-۳۳
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