Romain D R, Goldsmith J, Cairney H, Columbano-Green L M, Smythe R H, Parfitt R G
Cytogenetics Laboratory, Wellington Hospital, New Zealand.
J Med Genet. 1990 Sep;27(9):588-9. doi: 10.1136/jmg.27.9.588.
An 18 month old girl with partial monosomy for the long arm of chromosome 22 is described. The karyotype was 46,XX,del(22)(pter----q13.1::q13.33----qter). To our knowledge this is the first report of monosomy for this specific segment of chromosome 22. Clinical features include developmental delay in all areas, hypotonia, macrosomia, full cheeks, eyebrows, and eyelids, mild epicanthus, wide nasal bridge, long philtrum, and thick lower lip. Parental chromosome studies were normal.
本文描述了一名18个月大的女童,其22号染色体长臂存在部分单体性。核型为46,XX,del(22)(pter----q13.1::q13.33----qter)。据我们所知,这是22号染色体这一特定区段单体性的首例报告。临床特征包括各方面发育迟缓、肌张力减退、巨大儿、脸颊丰满、眉毛和眼睑浓密、轻度内眦赘皮、鼻梁宽、人中长以及下唇厚。父母的染色体检查正常。