家族性桡尺骨融合
Familial radioulnar synostosis.
作者信息
Spritz R A
出版信息
J Med Genet. 1978 Apr;15(2):160-2. doi: 10.1136/jmg.15.2.160.
Abstract
A family with proximal radioulnar synostosis segregating in three generations is described. Familial radioulnar synostosis is a rare anomaly; however, the sporadic form is a frequent feature in cases of sex chromosome abnormalities and other syndromes. This disorder has been reported in several ethnic groups, but this is apparently the first example from the black population.
摘要
本文描述了一个家系，近端桡尺关节融合在三代人中呈分离状态。家族性桡尺关节融合是一种罕见的异常情况；然而，散发型在性染色体异常和其他综合征病例中是常见特征。该疾病已在多个种族群体中报道，但这显然是来自黑人人群的首个病例。
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本文引用的文献
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Swivel for proximal radio-ulnar synostosis.用于近端桡尺关节融合的旋转装置。
J Bone Joint Surg Am. 1957 Jul;39-A(4):945-52.
2
Radioulnar synostosis, behavioral disturbance, and XYY chromosomes.桡尺骨骨性连接、行为障碍与XYY染色体
J Pediatr. 1969 Jan;74(1):103-6. doi: 10.1016/s0022-3476(69)80014-4.
3
Radioulnar synostosis. A common occurrence in sex chromosomal abnormalities.桡尺骨融合。在性染色体异常中很常见。
Am J Dis Child. 1971 Jul;122(1):10-1.
4
Congenital radio-ulnar synostosis. Report of 37 cases.先天性桡尺骨融合。37例报告。
Acta Orthop Scand. 1970;41(3):225-30. doi: 10.3109/17453677008991509.
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Radioulnar synostosis and craniosynostosis in one family.一个家族中的桡尺骨融合和颅缝早闭
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