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先天性倒转型内眦赘皮、睑裂狭小、上睑下垂及双眼内眦距离增宽综合征,Bergin等已将其正式命名为Komoto综合征.此病符合常染色体显性遗传规律.作者采取手术治疗,既解决美容,又达到治疗的目的,现报告如下.宋×,女,8岁,住院号363312,思儿出生后即有双眼上睑下垂,睑裂狭小,皱眉视物.父母非近亲婚配,家族中父亲及弟弟有类似眼病.全身检查无特殊发现.眼部检查:双眼视力0.6,不能矫正.双眼上睑下垂,睑裂长16mm,平视睑裂宽2mm,向上注视宽3mm,向下注视1.5mm.双眼倒转型内眦赘皮.双眼内毗距离40mm.上睑提肌无力.双眼球大小、运动及眼位正常,鼻梁低平.
Congenital inverted epicanthus, palpebral fissure narrowing, ptosis and binocular broadenation syndrome, Bergin, etc. It has been officially named Komoto syndrome. The disease consistent with autosomal dominant genetic law. The authors take Surgical treatment, both to solve the cosmetic, but also to achieve the purpose of treatment, are as follows.SONG ×, female, 8 years old, hospital number 363312, thinking children after birth, there are double-sided ptosis, palpebral fissure narrow, frowning material. Inbred marriage, the family father and brother have similar eye disease .Special body examinationNo special discovery.Ophthalmoscopy: binocular vision 0.6, can not be corrected.Plain ptosis, palpebral fissure length 16mm, flat palpebral fissure width 2mm, upwards wide 3mm, Eyes down 1.5mm. Eyes inverted epicanthus epidermis. Eyes within the adjacent distance 40mm. Levator levator muscle weakness. Double eyeball size, movement and eye position normal, low nose.