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家族性前脑无裂畸形、心脏缺陷和多指畸形。

Familial holoprosencephaly, heart defects, and polydactyly.

作者信息

Hennekam R C, van Noort G, de la Fuente A A

机构信息

Clinical Genetics Center, Utrecht, The Netherlands.

出版信息

Am J Med Genet. 1991 Nov 1;41(2):258-62. doi: 10.1002/ajmg.1320410226.

Abstract

We describe a pair of sibs with microcephaly, hypoplastic nose, cleft lip/palate, a complicated Fallot-like cardiac defect, and holoprosencephaly and polydactyly. One sib appeared to have normal chromosomes. The healthy parents were second cousins. This constellation of signs has been described before in at least 14 other patients, and was possibly present in several others. Although there is overlap with a number of similar conditions, especially hydrolethalus syndrome, this probably represents a separate entity. Three pairs of sibs and consanguinity in 3 families point to autosomal recessive pattern of inheritance.

摘要

我们描述了一对患有小头畸形、鼻发育不全、唇腭裂、复杂的法洛四联症样心脏缺陷、前脑无裂畸形和多指畸形的同胞。其中一个同胞的染色体似乎正常。健康的父母是二级表亲。至少在其他14名患者中也曾描述过这种体征组合,可能还有其他一些患者也存在。尽管与许多类似病症有重叠,尤其是水脑致死综合征,但这可能代表一种独立的病症。3个家族中有3对同胞及近亲结婚,提示为常染色体隐性遗传模式。

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