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弯肢侏儒症

Campomelic dysplasia.

作者信息

Jain Vineet, Sen Biswaroop

机构信息

aSports Injury Centre, Safdarjang Hospital bDepartment of Orthopaedics, St Stephen's Hospital, Delhi, India.

出版信息

J Pediatr Orthop B. 2014 Sep;23(5):485-8. doi: 10.1097/BPB.0000000000000058.

Abstract

Campomelic dysplasia is a rare hereditary congenital osteochondral dysplasia characterized by abnormal bowing of the lower limbs, sex reversal in males, and other skeletal and extraskeletal abnormalities. It is usually fatal in the neonatal period because of respiratory insufficiency. The diagnosis is usually difficult because of its rare presentation and the prognosis is poor. We present such a case in a 1-month-old child with typical skeletal abnormalities, whose presentation was unusual because of later presentation of respiratory distress and lack of genitourinary abnormalities.

摘要

弯肢侏儒症是一种罕见的遗传性先天性骨软骨发育不良,其特征为下肢异常弯曲、男性性别反转以及其他骨骼和骨骼外异常。由于呼吸功能不全,该病在新生儿期通常是致命的。由于其罕见的表现,诊断通常很困难,且预后不良。我们报告了一名1个月大患有典型骨骼异常的患儿病例,该病例的表现不寻常,因为呼吸窘迫出现较晚且无泌尿生殖系统异常。

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