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普拉德-威利综合征中的新生儿呼吸抑制及诊断延迟

Neonatal respiratory depression and delay in diagnosis in Prader-Willi syndrome.

作者信息

Wharton R H, Bresnan M J

机构信息

Birth Defects Service, Children's Hospital, Harvard Medical School.

出版信息

Dev Med Child Neurol. 1989 Apr;31(2):231-6. doi: 10.1111/j.1469-8749.1989.tb03983.x.

Abstract

The authors retrospectively evaluated the diagnoses at four months of age for 48 individuals with known Prader-Willi syndrome. 15 had been diagnosed as having cerebral palsy, and at four months only two of the 48 had been correctly diagnosed as Prader-Willi syndrome. 11 (23 per cent) had had birth asphyxia, compared with an expected rate of 1 per cent. Other perinatal features which occurred more frequently than expected included breech presentation, decreased fetal movements and prolonged gestation. Failure to make an early diagnosis of Prader-Willi syndrome often results in later disability being blamed on the birth process, when instead the child's neonatal problems are secondary to a prenatal condition.

摘要

作者对48例已知普拉德-威利综合征患者在4个月大时的诊断情况进行了回顾性评估。15例曾被诊断为脑瘫,在4个月大时,48例中只有2例被正确诊断为普拉德-威利综合征。11例(23%)有出生时窒息,而预期发生率为1%。其他比预期更频繁出现的围产期特征包括臀位产、胎动减少和孕期延长。未能早期诊断普拉德-威利综合征常常导致后来的残疾被归咎于出生过程,而实际上孩子的新生儿问题是由产前状况引起的继发性问题。

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