出生前診断された1q部分モノソミー3q部分トリソミーの1例

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タイトル別名
  • Prenatal Diagnosis of Partial Monosomy 1q and Partial Trisomy 3q : A Case Report

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At 28 weeks' gestation, sonographic examinations revealed a fetus with overlapping fingers, enlargement of the cisterna magna and choroid plexus cysts. Chromosomal analysis of the fetal cord blood showed the presence of an abnormal chromosome 1, and his father's blood showed a balanced reciprocal translocation. The fetus therefore carried an unbalanced reciprocal translocation with the karyotype of 46, XY, der(1)t(1;3) (q44;q23)pat. At 33 weeks, a male infant, weight 1,494g and height 36cm with on Apgar score of 7/8 was spontaneously delivered. Physical examination revealed hirsutism, malformed and low set auricles, cleft palate, malformed fingers, cardiac defects, and brain anomaly.

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