首页> 外文期刊>American journal of medical genetics, Part A >A new Ehlers-Danlos syndrome with craniofacial characteristics, multiple congenital contractures, progressive joint and skin laxity, and multisystem fragility-related manifestations.
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A new Ehlers-Danlos syndrome with craniofacial characteristics, multiple congenital contractures, progressive joint and skin laxity, and multisystem fragility-related manifestations.

机译:具有颅面特征,多发性先天性挛缩,进行性关节和皮肤松弛以及与多系统脆弱性相关的表现的新型Ehlers-Danlos综合征。

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摘要

We previously described two unrelated patients showing characteristic facial and skeletal features, overlapping with the kyphoscoliosis type Ehlers-Danlos syndrome (EDS) but without lysyl hydroxylase deficiency [Kosho et al. (2005) Am J Med Genet Part A 138A:282-287]. After observations of them over time and encounter with four additional unrelated patients, we have concluded that they represent a new clinically recognizable type of EDS with distinct craniofacial characteristics, multiple congenital contractures, progressive joint and skin laxity, and multisystem fragility-related manifestations. The patients exhibited strikingly similar features according to their age: craniofacial, large fontanelle, hypertelorism, short and downslanting palpebral fissures, blue sclerae, short nose with hypoplastic columella, low-set and rotated ears, high palate, long philtrum, thin vermilion of the upper lip, small mouth, and micro-retrognathia in infancy; slender and asymmetric face with protruding jaw from adolescence; skeletal, congenital contractures of fingers, wrists, and hips, and talipes equinovarus with anomalous insertions of flexor muscles; progressive joint laxity with recurrent dislocations; slender and/or cylindrical fingers and progressive talipes valgus and cavum or planus, with diaphyseal narrowing of phalanges, metacarpals, and metatarsals; pectus deformities; scoliosis or kyphoscoliosis with decreased physiological curvatures of thoracic spines and tall vertebrae; cutaneous, progressive hyperextensibility, bruisability, and fragility with atrophic scars; fine palmar creases in childhood to acrogeria-like prominent wrinkles in adulthood, recurrent subcutaneous infections with fistula formation; cardiovascular, cardiac valve abnormalities, recurrent large subcutaneous hematomas from childhood; gastrointestinal, constipation, diverticula perforation; respiratory, (hemo)pneumothorax; and ophthalmological, strabismus, glaucoma, refractive errors.
机译:我们之前曾描述过两名不相关的患者,这些患者表现出特征性的面部和骨骼特征,与后凸型脊柱侧弯型埃勒斯-丹洛斯综合征(EDS)重叠,但没有赖氨酰羟化酶缺乏症[Kosho等(2005)Am J Med Genet Part A 138A:282-287]。经过一段时间的观察并与另外四名不相关的患者相遇后,我们得出的结论是,它们代表了一种临床上可识别的新型EDS,具有独特的颅面特征,多发性先天性挛缩,进行性关节和皮肤松弛以及与多系统脆弱性相关的表现。根据年龄的不同,患者表现出惊人的相似特征:颅面,大font门,肥大,睑裂短而向下倾斜,巩膜蓝,鼻梁短,发育不良小柱,耳朵低落和旋转,上颚高,腓骨长,唇ver薄。婴儿时期的上唇,小口和小白粉病;细长,不对称的脸,青春期时颌骨突出;手指,手腕和臀部的骨骼,先天性挛缩,以及与屈肌异常插入的滑石裂等;进行性关节松弛,反复脱位;细长的和/或圆柱形的手指以及渐进的滑石外翻和腔或平顶,骨指,掌骨和meta骨的骨干变窄;眼睑畸形脊柱侧凸或脊柱后凸畸形,胸椎和高脊椎的生理曲度降低;皮肤,进行性过度伸展,挫伤和脆弱性伴萎缩性瘢痕;儿童期手掌细微皱纹至成年后的肩峰状皱纹,皮下反复感染并形成瘘管;心血管,心脏瓣膜异常,儿童期复发性大皮下血肿;胃肠道,便秘,憩室穿孔;呼吸性(血)气胸;和眼科,斜视,青光眼,屈光不正。

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