Lagerström-Fermér M, Sundvall M, Johnsen E, Warne G L, Forrest S M, Zajac J D, Rickards A, Ravine D, Landegren U, Pettersson U
Department of Medical Genetics, Biomedical Center, University of Uppsala, Sweden.
Am J Hum Genet. 1997 Apr;60(4):910-6.
We present a linkage analysis and a clinical update on a previously reported family with X-linked recessive panhypopituitarism, now in its fourth generation. Affected members exhibit variable degrees of hypopituitarism and mental retardation. The markers DXS737 and DXS1187 in the q25-q26 region of the X chromosome showed evidence for linkage with a peak LOD score (Zmax) of 4.12 at zero recombination fraction (theta(max) = 0). An apparent extra copy of the marker DXS102, observed in the region of the disease gene in affected males and heterozygous carrier females, suggests that a segment including this marker is duplicated. The gene causing this disorder appears to code for a dosage-sensitive protein central to development of the pituitary.
我们报告了一个先前报道过的患有X连锁隐性全垂体功能减退症的家族的连锁分析及临床最新情况,该家族现已传至第四代。患病成员表现出不同程度的垂体功能减退和智力发育迟缓。位于X染色体q25 - q26区域的标记DXS737和DXS1187显示出与疾病连锁的证据,在零重组率(θ(max) = 0)时最大对数优势分数(Zmax)为4.12。在患病男性和杂合子携带者女性的疾病基因区域观察到标记DXS102明显有一个额外拷贝,这表明包含该标记的一段区域发生了重复。导致这种疾病的基因似乎编码一种对垂体发育至关重要的剂量敏感蛋白。