Wertelecki W, Smith L T, Byers P
Department of Medical Genetics, University of South Alabama, Mobile 36688.
J Pediatr. 1992 Oct;121(4):558-64. doi: 10.1016/s0022-3476(05)81144-8.
We describe initial observations of an infant with dermatosparaxis (another form of Ehlers-Danlos syndrome, designated as type VIIC), an autosomal recessive disorder characterized by skin fragility and described in several species of domesticated animals. Electron microscopic examination of the skin shows collagen sheets rather than fibrils, and characteristic distortions resembling hieroglyphs. In addition to skin fragility, the disorder is characterized by redundant skin folds and edema, healing with minimal scar formation, large fontanels and wide sagittal and metopic sutures, blue sclerae, micrognathia, and umbilical hernia; after the neonatal period there are joint laxity, growth failure, short limbs, and normal mineralization of the skeleton except for the cranial vault. This disorder may also be a cause of premature rupture of placental membranes and myopia.
我们描述了一名患有皮肤松垂症(埃勒斯-当洛综合征的另一种形式,命名为VII C型)婴儿的初步观察结果,这是一种常染色体隐性疾病,其特征为皮肤脆弱,在几种家养动物中也有描述。对皮肤进行电子显微镜检查显示为胶原片而非纤维,以及类似象形文字的特征性扭曲。除皮肤脆弱外,该疾病的特征还包括多余的皮肤褶皱和水肿、愈合时瘢痕形成极少、囟门大以及矢状缝和额缝宽、巩膜呈蓝色、小颌畸形和脐疝;新生儿期过后会出现关节松弛、生长发育迟缓、四肢短小以及除颅顶外骨骼矿化正常。这种疾病也可能是胎膜早破和近视的一个原因。