Park J P, Wurster-Hill D H, Andrews P A, Cooley W C, Graham J M
Department of Pathology, Dartmouth-Hitchcock Medical Center, Hanover, New Hampshire.
Clin Genet. 1987 Nov;32(5):342-8. doi: 10.1111/j.1399-0004.1987.tb03299.x.
Analysis of partial duplication of chromosome 21 suggests that band 21q22 contains determinants for the Down syndrome. We report two cases of free proximal trisomy 21 without manifestations of the Down syndrome. Phenotypic anomalies included marked microcephaly, short stature, hypoplastic nails, and mental retardation/developmental delay. Our cases are consistent with the assignment of band 21q22 as the causal duplicated segment in the Down syndrome.
对21号染色体部分重复的分析表明,21q22带含有唐氏综合征的决定因素。我们报告了两例游离近端21三体而无唐氏综合征表现的病例。表型异常包括明显小头畸形、身材矮小、指甲发育不全以及智力迟钝/发育迟缓。我们的病例与将21q22带认定为唐氏综合征中导致重复的片段一致。