Alternative surgical methods for ptosis in patients with 18p deletion syndrome.
作者信息
Han Sang Beom
机构信息
Department of Ophthalmology, Kangwon National University Hospital, Kangwon National University Graduate School of Medicine, Chuncheon, South Korea.
出版信息
Int Med Case Rep J. 2017 Mar 22;10:97-98. doi: 10.2147/IMCRJ.S133748. eCollection 2017.
Abstract
摘要
相似文献
1
Alternative surgical methods for ptosis in patients with 18p deletion syndrome.18p缺失综合征患者上睑下垂的替代手术方法。
Int Med Case Rep J. 2017 Mar 22;10:97-98. doi: 10.2147/IMCRJ.S133748. eCollection 2017.
2
A case of de novo 18p deletion syndrome with panhypopituitarism.一例新发18p缺失综合征伴全垂体功能减退症。
Ann Pediatr Endocrinol Metab. 2019 Mar;24(1):60-63. doi: 10.6065/apem.2019.24.1.60. Epub 2019 Mar 31.
3
Monosomy 18p is a risk factor for facioscapulohumeral dystrophy.单体型 18p 是面肩肱型肌营养不良症的一个风险因素。
J Med Genet. 2018 Jul;55(7):469-478. doi: 10.1136/jmedgenet-2017-105153. Epub 2018 Mar 21.
4
Towards mapping phenotypical traits in 18p- syndrome by array-based comparative genomic hybridisation and fluorescent in situ hybridisation.通过基于阵列的比较基因组杂交和荧光原位杂交绘制18p-综合征的表型特征图谱。
Eur J Hum Genet. 2007 Jan;15(1):35-44. doi: 10.1038/sj.ejhg.5201718. Epub 2006 Oct 4.
5
A case of 18p deletion syndrome after blepharoplasty.一例眼睑成形术后发生的18号染色体短臂缺失综合征。
Int Med Case Rep J. 2017 Jan 12;10:15-18. doi: 10.2147/IMCRJ.S123938. eCollection 2017.
6
Characteristics of dystonia in the 18p deletion syndrome, including a new case.18p缺失综合征中肌张力障碍的特征，包括1例新病例。
Clin Neurol Neurosurg. 2009 Dec;111(10):880-2. doi: 10.1016/j.clineuro.2009.07.013. Epub 2009 Aug 20.
7
A rare case of de novo mosaicism: Deletion 18p and isochromosome 18q syndrome.一例罕见的新发嵌合体病例：18号染色体短臂缺失和18号染色体长臂等臂染色体综合征。
J Pediatr Genet. 2013 Sep;2(3):141-6. doi: 10.3233/PGE-13058.
8
Optic disk and white matter abnormalities in a patient with a de novo 18p partial monosomy.一名新发18p部分单体患者的视盘和白质异常
Ophthalmic Genet. 2010 Sep;31(3):147-54. doi: 10.3109/13816810.2010.492817.
9
Dental caries history in nine children with chromosome 18p deletion syndrome.9名18号染色体短臂缺失综合征患儿的龋齿病史。
Spec Care Dentist. 2000 Mar-Apr;20(2):53-5. doi: 10.1111/j.1754-4505.2000.tb01143.x.
10
Midline defects in deletion 18p syndrome: clinical and molecular characterization of three patients.18p缺失综合征的中线缺陷：三例患者的临床和分子特征
Clin Dysmorphol. 2007 Oct;16(4):247-52. doi: 10.1097/MCD.0b013e328235a572.
本文引用的文献
1
A case of 18p deletion syndrome after blepharoplasty.一例眼睑成形术后发生的18号染色体短臂缺失综合征。
Int Med Case Rep J. 2017 Jan 12;10:15-18. doi: 10.2147/IMCRJ.S123938. eCollection 2017.
2
Maximal levator resection in unilateral congenital ptosis with poor levator function.提上睑肌功能不良的单侧先天性上睑下垂的最大提上睑肌切除术
Br J Ophthalmol. 2017 Jun;101(6):740-746. doi: 10.1136/bjophthalmol-2016-309163. Epub 2016 Sep 6.
3
Treatment of unilateral congenital ptosis: putting the debate to rest.单侧先天性上睑下垂的治疗：终结争议。
Curr Opin Ophthalmol. 2013 Sep;24(5):484-7. doi: 10.1097/ICU.0b013e328363861a.
Zotero 插件