- A Case of Type 2 Usher Syndrome
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Boo SH, Park DJ, Han CS
- KMID: 2276936
- Korean J Otorhinolaryngol-Head Neck Surg.
- 2008 Sep;51(9):833-837.
The Usher syndrome is an autosomal recessive disorder that cause bilateral sensorineural hearing loss and progressive loss of vision. It is genetically heterogeneous and is the most frequent cause of... -
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- Two Cases Usher's Syndrom in two Brothers
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Kim KH, Lee SJ, Lee HK
- KMID: 2107829
- J Korean Ophthalmol Soc.
- 1995 Jan;36(1):153-159.
Usher's syndrome is an autosomal recessively inherited trait that characterized by a congenital nonprogressive sensorineural hearing impairment and progressive night-blinding disorder, retinitis pigmentosa, with cataract, psych psis, speech disorder, mental... -
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- A Case of Usher Syndrome
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Kim LS, Han CS, O YJ, Kim DW, Hur JW
- KMID: 2074447
- Korean J Otolaryngol-Head Neck Surg.
- 2001 Oct;44(10):1112-1115.
The usher syndrome (US) is an autosomal recessive disorder characterized by congenital bilateral sensorineural hearing loss and progressive visual loss secondary to retinitis pigmentosa. It is the most common cause... -
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- The Clinical Manifestations of Usher Syndrome in Korea
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Han SB, Kim SJ, Kim JH, Choung HK, Yu YS
- KMID: 2021431
- J Korean Ophthalmol Soc.
- 2007 Jul;48(7):950-956.
PURPOSE: To obtain useful information for counseling patients with Usher syndrome by analyzing the characteristics of its ophthalmologic manifestations. METHOD: The records of eight patients were reviewed for visual acuity, refractive... -
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- A Novel Frameshift Mutation of the USH2A Gene in a Korean Patient with Usher Syndrome Type II
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Boo SH, Song MJ, Kim HJ, Cho YS, Chu H, Ko MH, Chung WH, Kim JW, Hong SH
- KMID: 2278520
- Clin Exp Otorhinolaryngol.
- 2013 Mar;6(1):41-44.
Usher syndrome type II (USH2) is the most common form of Usher syndrome, characterized by moderate to severe hearing impairment and progressive visual loss due to retinitis pigmentosa. It has... -
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- A Case of Type 1 Ushers Syndrome with Bilateral Cataract
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Lee SJ, Lee JH, Choi YJ, Kim JW
- KMID: 2205301
- J Korean Ophthalmol Soc.
- 1998 Apr;39(4):784-789.
Ushers syndrome is an autosomal recessively inherited entity which is characterized by a retinitis pigmentosa and congenital sensorineural hearing loss. This syndrome represents different clinical features according to its subtypes.... -
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- Type IV Ushers Syndrome Manifested by Woman
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Kim SH, Koo HM, Chung SK
- KMID: 1952501
- J Korean Ophthalmol Soc.
- 1997 Jul;38(7):1289-1293.
Ushers syndrome is an autosomal recessively inherited trait that characterized by progressive retinitis pigmentosa combining night blindness with a congenital, nonprogressive sensorineural hearing impairment of variable severity. Speech disorder, vestibular... -
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