- Two Cases of Oculopharyngeal Muscular Dystrophy in One Family
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Suh MW, Lee KH, Rho JK, Myong HJ
- KMID: 2044096
- J Korean Neurol Assoc.
- 1984 Dec;2(2):208-216.
The authors encountered 2 siblings who showed progressive ophthalmoplegia and bulbar palsy. The patients were studied with various laboratory aids and thought to be as oculopharyngeal muscular dystrophy. The oculopharyngeal... -
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- A Case of Oculopharyngeal Muscular Dystrophy
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Kim MH, Chung SK, Park C
- KMID: 1949601
- J Korean Ophthalmol Soc.
- 1991 Dec;32(12):1153-1158.
Oculopharyngeal muscular dystrophy, one of the variants of chronic progressive external ophthalmoplegia, is a disorder characterized by progressive bilateral ptosis, immobility of the eyes and dysphagia. We have experienced a... -
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- A Family of Oculopharyngeal Muscular Dystrophy and it's HLA Typing
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Yi SD, Park YC, Chung TH
- KMID: 1662008
- J Korean Neurol Assoc.
- 1986 Dec;4(2):266-272.
The authors presented a family whose 4 siblings had been suffered from oculopharyngeal muscular dystrophy of autoscmal recessive trend, with symptoms of progressive ptosis, external ophthalmoplegia, dysarthria, dysphagia and facial... -
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- A case of oculopharyngeal muscular dystrophy: electrophysiological review
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Kang SY, Yang SH, Song DH, Nam SH
- KMID: 1688120
- J Korean Acad Rehabil Med.
- 1991 Sep;15(3):377-383.
No abstract available. -
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- A Case of the Oculopharyngeal Muscular Dystrophy
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Lee JB, Kim KC, Bum SG
- KMID: 2336426
- J Korean Ophthalmol Soc.
- 1987 Apr;28(2):489-494.
The oculopharyngeal muscular dystrophy is a distinct, clinically well-defined myopathy of later life inherited in an autosomal dominant fashion with complete penetrance. Blepharoptosis, dysphagia, lower leg weakness are the most... -
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- Correction of blepharoptosis in oculopharyngeal muscular dystrophy: cases in one family
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No authors listed
- KMID: 2204118
- J Korean Soc Plast Reconstr Surg.
- 1998 Oct;25(7):1353-1358.
Oculopharyngeal muscular dystrophy is a hereditary, autosomal dominant, slowly progressive disorder with middle age onset, major symptoms are ptosis and dysphagia mainly due to selectively involved levator palpebrae and the... -
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- A Case of Oculopharyngeal Muscular Dystrophy Due to a Novel Mutation of the PABPN1 Gene
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Bae JS, Kim MK, Ki CS, Kim JW, Kim BJ
- KMID: 2343154
- J Korean Neurol Assoc.
- 2005 Apr;23(2):278-281.
We recently encountered a Korean patient with oculopharyngeal muscular dystrophy (OPMD). His major clinical manifestations were late onset bilateral ptosis, dysarthria, and dysphagia. Direct sequencing analysis of the PABPN1 gene... -
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- Frontalis Suspension Using a Silicone Rod in Blepharoptosis Patients with Poor Ocular Motility
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Choi YJ, Kim YD
- KMID: 2211483
- J Korean Ophthalmol Soc.
- 2008 Apr;49(4):548-554.
- doi: 10.3341/jkos.2008.49.4.548
PURPOSE: To determine the efficacy of frontalis sling operation with silicone rods in patients with compromised corneal protective mechanisms. METHODS: The authors retrospectively studied 6 consecutive patients (7 eyelids) with severe... -
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