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Two rare cases of 6p partial deletion.

作者信息

Jalal S M, Macias V R, Roop H, Morgan F, King P

机构信息

Genetic Screening and Counseling Service, Denton, Texas.

出版信息

Clin Genet. 1989 Sep;36(3):196-9. doi: 10.1111/j.1399-0004.1989.tb03188.x.

Abstract

Two rare cases of 6p partial deletion (6p23----pter) are described. Both patients are at or past the adolescent stage, with severe mental retardation and severe to moderate developmental retardation. Physical dysmorphic features that stand out are: short forehead, borderline microcephaly, low-set malformed ears, hyperplastic nares, dental anomalies and short terminal phalanges. The diversity of the phenotypic features has considerable variations in patients with ring of 6, apparently reflecting the relative loss of p and q arms. A case of a larger terminal deletion and a report of an interstitial deletion is also reviewed.

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