[刚果新生儿致死性成骨不全]。

Archives francaises de pediatrie Pub Date : 1993-12-01
G Moyen, J L Nkoua, M Pongui, A M Mafouta, S Nzingoula
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引用次数: 0

摘要

背景:几种形式的成骨不全已被描述。围产期致死形式(II型沉默)根据放射学特征被细分为A、B和C组。本报告描述一个IIA型病例。病例报告:一名刚果女婴足月出生健康,非近亲父母。妊娠期间未做超声检查。新生儿出生时患有急性呼吸窘迫。临床检查表现为骨骼异常:四肢缩短、弯曲,活动时产生震颤,颅骨柔软,胸腔狭窄。x光显示短而宽、弯曲的长骨有骨折的迹象;肋骨很细,呈珠状;在头骨中发现了虫骨。新生儿在出生5小时时死于呼吸窘迫。父母、哥哥和堂兄弟的临床和x光检查均正常。结论:这名婴儿似乎患有一种致命的成骨不全症,可能是沉默型IIA。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Lethal osteogenesis imperfecta in a Congolese newborn infant].

Background: Several forms of osteogenesis imperfecta have been described. The perinatally lethal forms (type II of Sillence) have been subclassified into groups A, B and C on the basis of radiological features. This report describes a case of type IIA.

Case report: A female Congolese baby was born at term to healthy, non-consanguineous parents. No ultrasonographic studies were done during the pregnancy. The newborn suffered from acute respiratory distress at birth. Clinical examination showed bone abnormalities: shortened and bowed limbs with crepitation at mobilization, soft calvaria and narrow rib cage. X-rays showed short, broad, bowed long bones with signs of fractures; the ribs were thin and beaded; wormian bones were seen in the skull. The newborn died from respiratory distress at the age of 5 hours. All clinical and X-rays investigations of the parents, the elder brother and cousins were normal.

Conclusion: This baby seems to have suffered from a lethal form of osteogenesis imperfecta, probably type IIA of Sillence.

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