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Pallister Killian--mosaic tetrasomy 12 p syndrome. Another prenatally diagnosed case.

作者信息

Bresson J L, Arbez-Gindre F, Peltie J, Gouget A

机构信息

Laboratoire de Cytogénétique, CHRU de Besancon, France.

出版信息

Prenat Diagn. 1991 Apr;11(4):271-5. doi: 10.1002/pd.1970110409.

DOI:10.1002/pd.1970110409
PMID:1896413
Abstract

A new case of mosaic tetrasomy 12 p (46,XY/47,XY, +i12 p), diagnosed during pregnancy from ultrasonographic signs, is reported. We emphasize the peculiar position of the diaphragmatic hernia in this syndrome. Its presence or absence determines the vital prognosis and the age of diagnosis. The knowledge of its possible association with tetrasomy 12 p can contribute considerably to the neonatal diagnosis by directing the work of the cytogeneticist to tissue cultures which enable him to detect the presence of the tetrasomy.

摘要

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Pallister Killian--mosaic tetrasomy 12 p syndrome. Another prenatally diagnosed case.
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引用本文的文献

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Genetic considerations in the prenatal diagnosis of overgrowth syndromes.过度生长综合征产前诊断中的遗传学考量
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Pallister-Killian syndrome: normal karyotype in prenatal chorionic villi, in postnatal lymphocytes, and in slowly growing epidermal cells, but mosaic tetrasomy 12p in skin fibroblasts.帕利斯特-基利安综合征:产前绒毛膜绒毛、产后淋巴细胞及生长缓慢的表皮细胞的核型正常,但皮肤成纤维细胞存在12号染色体短臂的嵌合性四体。
J Med Genet. 1995 Jan;32(1):68-71. doi: 10.1136/jmg.32.1.68.