Berry A C, Whittingham A J, Neville B G
Arch Dis Child. 1981 Nov;56(11):882-5. doi: 10.1136/adc.56.11.882.
Three children with Prader-Willi syndrome and chromosome abnormalities affecting chromosome 15 are described and the literature is reviewed. The usefulness of chromosome analysis in the investigation of the floppy infant is illustrated by two of the cases described. Twenty-three other children with similar clinical features had normal chromosomes.
本文描述了3例患有普拉德-威利综合征且染色体异常累及15号染色体的儿童,并对相关文献进行了综述。所描述的其中2例病例说明了染色体分析在松软婴儿检查中的作用。另外23例具有相似临床特征的儿童染色体正常。