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A Case of Freeman-Sheldon Syndrome

Park HK, Byun YJ, Yoon JS, Lee SY

  • KMID: 2110577
  • J Korean Ophthalmol Soc.
  • 2007 Jun;48(6):845-848.
PURPOSE: To report a patient with Freeman-Sheldon syndrome with blepharophimosis. METHODS: A 4-year-old girl with congenital facial abnormalities consistent with Freeman-Sheldon syndrome presented with complaints of blepharophimosis. The characteristic features of...
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Consenital blepharophimosis with family history

Kim HO, Lee KH, Chung SM, You SJ, Kim SS

  • KMID: 1921376
  • J Korean Soc Plast Reconstr Surg.
  • 1993 Sep;20(5):1058-1063.
No abstract available.
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Surgical Correction of the Blepharophimosis Syndorome

Kim YD, Kim YS

  • KMID: 2123172
  • J Korean Ophthalmol Soc.
  • 1993 Oct;34(10):936-942.
During the past decade the syndorome of blepharoptosis, blepharophimosis, epicanthus inversus and telecanthus(blepharophimosis syndrome)have become recognized as a distinct tetrad based upon clinical and hereditary characteristics. Early surgery is recommended...
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A Case of Congenital Ptosis

Hah MC, Hong SH

  • KMID: 1902519
  • J Korean Ophthalmol Soc.
  • 1973 Mar;14(1):31-34.
A case of bilateral congenital ptosis with strong heredity. studied and treated at eye clinic in S.R.C.H. is reported. The ptosis was associated with external ophthalmoplegia and blepharophimosis in both...
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The Effects of Transnasal Wiring on the Congenital Telecanthus associated with Blepharophimosis, Blepharoptosis and Epicanthus Inversus

Lee IS, Lee TS

  • KMID: 2042571
  • J Korean Ophthalmol Soc.
  • 1986 Dec;27(6):1077-1081.
Telecanthus is abnormal widening between the medial canthi. There are two kinds of telecanthus which are congenital and acquired. Many authors have described and reported about the surgical procedures and...
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Repair of Telecanthus with Titanium Miniplate in Blepharophimosis Syndrome

Baek SH, Kim KS, Park BW, Lee TS

  • KMID: 2124744
  • J Korean Ophthalmol Soc.
  • 2000 May;41(5):1224-1228.
Telecanthus in congenital blepharophimosis has traditionally been repaired with conventional methods such as medial canthal tendon tucking and transnasal wiring.We report 2 cases of patients with telecanthus who underwent repair...
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A Case of Marden-Walker Syndrome

Cho HJ, Lee YK, Kim DU, Choi BJ, Kim JT, Lee IJ, Ji JG

  • KMID: 2335466
  • J Korean Pediatr Soc.
  • 1999 Oct;42(10):1471-1474.
Marden-Walder syndrome is characterized by a mask-like face, blepharophimosis, joint contractures, and psychometer retardation. We report a newborn infant with the clinical features of the syndrome. He was diagnosed with...
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Two case of Congenital Anophthalmos

Sohn KS, Shin IS, Kim JH, Kim SM, Shin KS

  • KMID: 1675798
  • J Korean Ophthalmol Soc.
  • 1969 Mar;10(1):11-13.
Authors observed clinically for congenital anophthalmos in two cases. One case was a boy, aged 6 years, having congenital anophthalmos of right eye with bifid uvula and another case was...
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The Effect of The Levator Resection on Congenital Blephareptesis

Jung YS, Park BK

  • KMID: 2204681
  • J Korean Ophthalmol Soc.
  • 1982 Sep;23(3):491-497.
Authors studied 73 patients(91 eyes) of the congenital blepharoptosis who were received the levator resection at Busan National University Hospital during recent 4 years and could do follow up studies...
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Romberg's Syndrome

Kim YJ, Hong YJ, Kim HB

  • KMID: 2107339
  • J Korean Ophthalmol Soc.
  • 1979 Dec;20(4):567-571.
The Romberg's syndrome is characterized by unilateral facial hemiatrophy. Romberg's syndrome becomes manifest in 10 or 20 decades, and involves skin, subcutaneous tissue, muscle, cartilage and bone of one side...
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Anesthetic managements for repair of atrial septal defect in a patient with Young-Simpson Syndrome: A case report

Kim SH, Kim TY, Jung HS, Kang JE, Oh CS, Kim DK, Yoon TG

Young-Simpson Syndrome (YSS) is a rare malformation syndrome characterized by facial dysmorphism, congenital heart abnormalities, congenital hypothyroidism and severe growth retardation. A 5-month-old girl was scheduled to undergo patch closure...
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Anesthesia of a patient with Dubowitz syndrome: A case report

Lee MK, Lee YS

Dubowitz syndrome is a rare autosomal recessive disorder that leads to growth retardation (intrauterine, postnatal), mental retardation, a peculiar face, microcephaly, behavioral problems and eczema. The peculiar face of individuals...
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Clinical Examination on the Blepharoptosis and the Resection of the Levator Muscle

Youn DY, Sung MK, Lee KH

  • KMID: 2122933
  • J Korean Ophthalmol Soc.
  • 1990 Feb;31(2):125-133.
The resection of levator aponeurosis and its muscle through the anterior approach had been performed on 50 ptotic lids of 40 patients from April, 1985 to January, 1988. Their age...
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Effect of the Simultaneous Operation of Levator Resection and Frontalis Suspension for Congenital Ptosis

Kim AR, Choi CW, Kim SD

PURPOSE: To determine retrospectively if a simultaneous frontalis suspension could change the result of undercorrection observed during levator resection in congenital ptosis patients with poor levator functions. METHODS: Eight eyes in...
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Epicanthoplasty Using Y-V Advancement Flap Method

Kim SJ, Song I, Choi JH, Lee JH, You YJ, Koh IS

  • KMID: 2120369
  • J Korean Soc Plast Reconstr Surg.
  • 2009 Mar;36(2):200-204.
PURPOSE: The epicanthal fold is a unique finding in the medial canthal area of many Asians. Various methods have been developed to eliminate this fold. However, excessive and prominent scarring...
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