首页> 外文期刊>International Journal of Otolaryngology and Head & Neck Surgery >Carotid Artery Prolapse and Myringocarotidopexy in Osteogenesis Imperfecta
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Carotid Artery Prolapse and Myringocarotidopexy in Osteogenesis Imperfecta

机译:成骨不全症中的颈动脉脱垂和Myringocarotidopexy。

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Osteogenesis Imperfecta is a rare genetic disorder of connective tissue that is caused by an error in collagen formation. The disease is characterized by abnormal bone fragility, osteopenia, blue discoloration of the sclerae and hearing loss. Chronic non-suppurative otitis media is frequent in Osteogenesis Imperfecta patients and usually attributed to Eustachian tube dysfunction due to cranial molding and deformities. In some cases of severe Osteogenesis Imperfecta, the fragile bone of the petrous carotid canal can be broken down by the pulsations of the carotid artery, this may result in prolapse of the carotid artery into the protympanum with resultant Eustachian tube obstruction and tympanic membrane retraction with adhesion to prolapsed carotid artery, a condition called myringocarotidopexy.
机译:成骨不全是一种罕见的结缔组织遗传病,由胶原蛋白形成错误引起。该疾病的特征是异常的骨骼脆弱性,骨质减少,巩膜发蓝变色和听力下降。慢性非化脓性中耳炎在成骨不全症患者中很常见,通常归因于颅骨成型和畸形引起的咽鼓管功能障碍。在某些严重的成骨不全症病例中,颈动脉搏动可破坏颈动脉的脆弱骨,这可能导致颈动脉脱垂进入鼓膜,并导致咽鼓管阻塞和鼓膜回缩黏附于脱垂的颈动脉,称为myringocarotidopexy。

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