Wilson M, Mulley J, Gedeon A, Robinson H, Turner G
Department of Medical Genetics, Prince of Wales Children's Hospital, Randwick, Sydney, Australia.
Am J Med Genet. 1991 Sep 15;40(4):406-13. doi: 10.1002/ajmg.1320400405.
We describe 14 males from 3 successive generations in a family who have X-linked mental retardation (XLMR), obesity, gynecomastia, speech difficulties, emotional lability, tapering fingers, and small feet. Linkage analysis using markers spread along the X chromosome demonstrated a gene localisation close to the centromere. Maximum lod scores for markers near the centromere, all at theta = 0.00, were 1.36 for DXS72, and 1.46 for DXYS1. The closest flanking markers which showed recombination were DXS84 and DXS94, defining the physical localisation within Xp21.1-q22. DXS255 was fully informative with lod-1 confidence interval for theta of 0.00-0.12. Clinical findings and linkage data in this family distinguish it from the Börjeson-Forssman-Lehmann syndrome and other previously described XLMR syndromes.
我们描述了一个家族中连续三代的14名男性,他们患有X连锁智力迟钝(XLMR)、肥胖、男性乳房发育、言语困难、情绪不稳定、手指变细和脚小。使用沿X染色体分布的标记进行连锁分析表明,有一个基因定位于靠近着丝粒的位置。着丝粒附近标记的最大对数优势分数,在θ = 0.00时,DXS72为1.36,DXYS1为1.46。显示重组的最紧密侧翼标记是DXS84和DXS94,确定了其物理定位在Xp21.1-q22内。DXS255在θ为0.00-0.12时具有完全信息性,对数优势置信区间为-1。该家族的临床发现和连锁数据将其与Börjeson-Forssman-Lehmann综合征及其他先前描述的XLMR综合征区分开来。