Ogata T, Goodfellow P, Petit C, Aya M, Matsuo N
Human Molecular Genetics Laboratory, Imperial Cancer Research Fund, London.
J Med Genet. 1992 Jul;29(7):455-9.
This report describes a Japanese girl with short stature and a rearranged X chromosome. Her height remained below the 3rd centile growth curve for Japanese girls, and her predicted adult height (148.5 cm) was below her target height (163 cm) and target range (155 to 171 cm). Cytogenetic studies showed that the rearranged X chromosome was formed by a breakage at q26 and a transfer of the Xq fragment onto the tip of Xp. The abnormal X was always late replicating. No mosaicism was detected. Molecular analysis showed an Xp terminal deletion distal to DXYS15. Biochemical and radiological studies for short stature disclosed no abnormality. On the basis of height analysis of previous reports and a genotype-phenotype correlation of this patient, we propose that a growth gene(s) is present in the distal part of the pseudoautosomal region.
本报告描述了一名身材矮小且X染色体重排的日本女孩。她的身高一直低于日本女孩第3百分位生长曲线,其预测成年身高(148.5厘米)低于目标身高(163厘米)及目标范围(155至171厘米)。细胞遗传学研究表明,重排的X染色体是由q26处断裂以及Xq片段转移至Xp末端形成的。异常的X染色体总是复制延迟。未检测到嵌合体。分子分析显示DXYS15远端的Xp末端缺失。针对身材矮小的生化及放射学研究未发现异常。基于既往报告的身高分析及该患者的基因型-表型相关性,我们提出假常染色体区域远端存在生长基因。