College of Medicine, University of Oklahoma, Oklahoma City, Oklahoma, USA.
Am J Med Genet A. 2012 Nov;158A(11):2935-40. doi: 10.1002/ajmg.a.35613. Epub 2012 Sep 14.
We report on a 16-year-old female originally diagnosed with Marden-Walker syndrome due to features such as facial dysmorphism, several musculoskeletal anomalies, and atrial septal defect in addition to hypoplasia of the inferior vermis with normal-sized cerebellum and absence of the septum pellucidum. However, an SNP array performed at age 15 years detected a total of 142 Mb of long runs of homozygosity (ROH), and put the diagnosis in doubt. Using the Genomic Oligoarray and SNP array evaluation tool (http://www.ccs.miami.edu/ROH), CHST14 provided a "hit" as a gene mapping to the largest ROH region associated with a phenotype matching our patient's (if mutated). At that time, she was a cognitively intact, thin female with growth parameters below the 3rd percentile. Craniofacial features included microcephaly, midface hypoplasia, blepharophimosis, entropion, myopia, microretrognathia, and dental malocclusion. Musculoskeletal features included kyphoscoliosis, arachnodactyly, camptodactyly, and rocker-bottom feet with interphalangeal contractures. Her skin displayed large ecchymoses and poorly healed atrophic scars. Sequencing of CHST14 revealed a complex homozygous frameshift mutation involving a 7-bp deletion and an 11-bp insertion predicted to produce a truncated protein. This mutation was not seen in 100 controls of various ethnicities. Thus, our patient represents not only a novel (homozygous) mutation in CHST14, but is also the first patient with dermatan 4-O-sulfotransferase 1-deficient Ehlers-Danlos syndrome (adducted thumb-clubfoot syndrome) (DD-EDS ATCS) documented in the Western Hemisphere. Furthermore, our patient's central nervous system anomalies have not before been described in DD-EDS (ATCS).
我们报告了一例 16 岁女性病例,最初因面部畸形、多种骨骼肌肉异常和房间隔缺损,以及小脑正常大小的下蚓部发育不良和透明隔缺失而被诊断为 Marden-Walker 综合征。然而,15 岁时进行的 SNP 微阵列检测发现总共存在 142Mb 的长片段纯合性(ROH),这使诊断受到质疑。使用基因组寡核苷酸微阵列和 SNP 微阵列评估工具(http://www.ccs.miami.edu/ROH),CHST14 作为一个基因提供了“命中”,该基因映射到与我们患者表型匹配的最大 ROH 区域(如果发生突变)。当时,她是一个认知正常、消瘦的女性,生长参数低于第 3 百分位。颅面特征包括小头畸形、中面部发育不全、睑裂狭小、内翻、近视、小下颌和牙列不齐。骨骼肌肉特征包括脊柱侧凸后凸、蜘蛛指(趾)、指(趾)屈曲畸形和跗跖部 rocker 畸形,伴有指间关节挛缩。她的皮肤有大块瘀斑,愈合不良,有萎缩性瘢痕。CHST14 的测序显示存在一种复杂的纯合移码突变,涉及 7bp 缺失和 11bp 插入,预计会产生截短的蛋白。这种突变在 100 名来自不同种族的对照中均未发现。因此,我们的患者不仅代表了 CHST14 中的一种新(纯合)突变,而且也是第一个在西半球记录的缺乏 4-O-硫酸软骨素转移酶 1 的埃勒斯-当洛斯综合征(内收拇指-爪形足综合征)(DD-EDS ATCS)患者。此外,我们患者的中枢神经系统异常以前在 DD-EDS(ATCS)中没有描述过。