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一例患有并指(趾)畸形家族中的异常遗传。

Anomalous inheritance in a kindred with split hand, split foot malformation.

作者信息

Spranger M, Schapera J

机构信息

Department of Human Genetics, Medical School, University of Cape Town, Observatory, South Africa.

出版信息

Eur J Pediatr. 1988 Feb;147(2):202-5. doi: 10.1007/BF00442225.

Abstract

A South African family with autosomal dominant split hand, split foot (SHSF) malformation has been studied. The pedigree was unusual in that three unaffected siblings with normal parents had each produced affected offspring. New mutation, germinal mosaicism and autosomal recessive inheritance are unlikely. Possible explanations of this contentious situation may be an unstable premutation or non-penetrance due to an inhibiting factor associated with the gene responsible for SHSF. Pregnancy monitoring by ultrasound of unaffected close relatives of a person with SHSF is recommended.

摘要

对一个患有常染色体显性遗传的裂手裂足(SHSF)畸形的南非家庭进行了研究。该家系不同寻常之处在于,父母正常的三个未患病的同胞各自都生育了患病后代。新发突变、生殖腺嵌合体和常染色体隐性遗传不太可能。对于这种有争议的情况,可能的解释是由于与导致SHSF的基因相关的抑制因子,存在不稳定的前突变或基因非外显。建议对SHSF患者的未患病近亲进行超声孕期监测。

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