下颌大造口综合征深皮移植后上、下眼睑轮廓及位置的改变。

IF 0.9 Q4 OPHTHALMOLOGY
Tatiana Boza, Doris Quiroz, Mariana Nadais Aidar, Denny M Garcia, Antônio Augusto Velasco E Cruz
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引用次数: 0

摘要

巨口畸形综合征是一种罕见的先天性疾病,由常染色体显性TWIST2突变引起。这种情况的特点是皮肤多余,耳朵位置低,大口畸形,生殖器模糊,上下眼睑发育不全。短的前板,隔膜和提肌腱膜导致严重的角膜暴露在生命的最初几个小时。自1977年McCarthy和West首次报告以来,已有21例AMS病例被记录在案。我们报告一个新的AMS病例,定量分析眼睑裂的变化后,皮肤移植物在上和下平滑跗骨肌和外侧跗骨愈合。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Upper and lower eyelid contour and positional changes after deep skin grafts in ablepharon macrostomia syndrome.

Ablepharon macrostomia syndrome is a rare congenital disorder caused by autosomal-dominant TWIST2 mutations. This condition is characterized by redundant skin, low-set ears, macrostomia, ambiguous genitalia, and underdevelopment of the both upper and lower eyelids. The shortening of the anterior lamella, septum and levator aponeurosis lead to a severe corneal exposure within the first hours of life. Since McCarthy and West's first report in 1977, 21 AMS cases have been documented. We report a new AMS case with a quantitative analysis of palpebral fissure changes following skin grafts over the upper and lower smooth tarsal muscles and lateral tarsorrhaphy.

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来源期刊
CiteScore
2.40
自引率
9.10%
发文量
136
期刊介绍: Orbit is the international medium covering developments and results from the variety of medical disciplines that overlap and converge in the field of orbital disorders: ophthalmology, otolaryngology, reconstructive and maxillofacial surgery, medicine and endocrinology, radiology, radiotherapy and oncology, neurology, neuroophthalmology and neurosurgery, pathology and immunology, haematology.
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