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Pallister-Killian综合征(PKS)是一种罕见的染色体异常疾病,基因学特点是12号染色体短臂的异常所致,由于报道病例较少临床医师对该病了解有限,现报道1例12p染色
Pallister-Killian syndrome (PKS) is a rare chromosomal abnormality characterized by an abnormality in the short arm of chromosome 12. Due to the limited number of reported cases, clinicians have limited knowledge of the disease and one case of 12p staining