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锥体先天性缺失及其在遗传性疾病中的意义。

Congenital absence of pyramids and its significance in genetic diseases.

作者信息

Chow C W, Halliday J L, Anderson R M, Danks D M, Fortune D W

出版信息

Acta Neuropathol. 1985;65(3-4):313-7. doi: 10.1007/BF00687014.

Abstract

Bilateral absence of the pyramids, best assessed in transverse sections of the medulla oblongata, was found in 0.7% of 2,850 autopsies performed at the Royal Children's Hospital, Melbourne (Australia). A strong association with some forms of congenital aqueductal stenosis was observed and evaluated in further cases ascertained through other hospitals. The very strong association observed with X-linked congenital aqueduct stenosis may be useful diagnostically but must be evaluated in other centres. At least, the presence of pyramids seems strong evidence against this diagnosis. Absence of the pyramids was also observed in several known or new genetic syndromes - Meckel's syndrome, the HARD syndrome, two sisters with congenital aqueductal stenosis and polydactyly and two families with microcephaly and arthrogryposis.

摘要

在澳大利亚墨尔本皇家儿童医院进行的2850例尸检中,0.7%的病例发现双侧锥体缺如,这在延髓横断面上评估最为准确。观察到与某些形式的先天性导水管狭窄有很强的关联,并在通过其他医院确诊的更多病例中进行了评估。观察到与X连锁先天性导水管狭窄有极强的关联,这在诊断上可能有用,但必须在其他中心进行评估。至少,锥体的存在似乎是反对这一诊断的有力证据。在几种已知或新的遗传综合征中也观察到锥体缺如,如梅克尔综合征、HARD综合征、两名患有先天性导水管狭窄和多指畸形的姐妹,以及两个患有小头畸形和关节挛缩的家族。

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