Bosley Thomas M, Alorainy Ibrahim A, Salih Mustafa A, Aldhalaan Hesham M, Abu-Amero Khaled K, Oystreck Darren T, Tischfield Max A, Engle Elizabeth C, Erickson Robert P
The Neuro-ophthalmology Division, King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia.
Am J Med Genet A. 2008 May 15;146A(10):1235-40. doi: 10.1002/ajmg.a.32262.
We describe nine previously unreported individuals from six families who have homozygous mutations of HOXA1 and either the Bosley-Salih-Alorainy syndrome (BSAS) or the Athabascan brainstem dysgenesis syndrome (ABDS). Congenital heart disease was present in four BSAS patients, two of whom had neither deafness nor horizontal gaze restriction, thus raising the possibility that cardiovascular malformations might be a clinically isolated, or relatively isolated, manifestation of homozygous HOXA1 mutations. Two ABDS probands had relatively mild mental retardation. These individuals blur the clinical distinctions between the BSAS and ABDS HOXA1 variants and broaden the phenotype and genotype of the homozygous HOXA1 mutation clinical spectrum.
我们描述了来自六个家庭的九名此前未报告的个体,他们患有HOXA1纯合突变,且患有博斯利 - 萨利赫 - 阿洛拉尼综合征(BSAS)或阿萨巴斯卡脑干发育不全综合征(ABDS)。四名BSAS患者患有先天性心脏病,其中两名既无耳聋也无水平凝视受限,因此增加了心血管畸形可能是HOXA1纯合突变的临床孤立或相对孤立表现的可能性。两名ABDS先证者有相对轻度的智力障碍。这些个体模糊了BSAS和ABDS的HOXA1变体之间的临床区别,并拓宽了HOXA1纯合突变临床谱的表型和基因型。