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患有少汗性外胚层发育不良及新发(X;9)易位的女性。AnLy细胞系病例的临床记录。

Female with hypohidrotic ectodermal dysplasia and de novo (X;9) translocation. Clinical documentation of the AnLy cell line case.

作者信息

MacDermot K D, Hultén M

机构信息

Children's Hospital, Ladywood Middleway, Birmingham, UK.

出版信息

Hum Genet. 1990 May;84(6):577-9. doi: 10.1007/BF00210814.

Abstract

We present here a historical documentation of a female with X-linked hypohidrotic ectodermal dysplasia (XHED) and a de novo X/9 chromosome translocation. The patient was verbally reported by Dr. P.L. J. Cook to the HGM conference in 1973, but was subsequently lost to follow up. We have since traced her and confirmed the diagnosis of XHED with moderately severe mental retardation. According to Dr. P. L. J. Cook's records, fibroblast cell line AnLy GMO 705, was derived from this patient. Another female with a de novo X/12 chromosome translocation and hypohidrotic ectodermal dysplasia was recently reported. In both cases, the X chromosome breakpoint appears to be at Xq13.1.

摘要

我们在此展示一名患有X连锁少汗性外胚层发育不良(XHED)并伴有新发X/9染色体易位的女性的历史记录。1973年,P.L.J.库克医生在人类基因定位会议上口头报告了该患者,但随后失去了随访。此后我们追踪到了她,并确诊其患有XHED且伴有中度严重智力障碍。根据P.L.J.库克医生的记录,成纤维细胞系AnLy GMO 705源自该患者。最近有报道称另一名患有新发X/12染色体易位和少汗性外胚层发育不良的女性。在这两个病例中,X染色体断点似乎都在Xq13.1处。

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