- The Laurence-Moon-Biedl Syndrome in a Family
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Choi DU, Kim YK, Lee JH
- KMID: 2107600
- J Korean Ophthalmol Soc.
- 1989 Oct;30(5):847-853.
Laurence-Moon-Biedl syndrome is a rare inherited disorder and its common findings include pigmentary retinal degeneration, obesity, hypogonadism, mental retardation and digital anomaly. Recently, the authors experienced two cases of Laurence-Moon-Biedl... -
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- A Case of Laurence-Moon-Biedl Syndrome Including Diabetic Mellitus
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Lee BH, Cho BR, Lee MI, Sohn KC, Yoo HJ
- KMID: 1682841
- J Korean Pediatr Soc.
- 1989 Jun;32(6):857-861.
No abstract available. -
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- A Case of Laurence-Moon-Biedl Syndrome
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Jeon PK, Ohn YH, Park JO, Kim CH
- KMID: 1601081
- Korean J Pediatr Gastroenterol Nutr.
- 2003 Mar;6(1):78-83.
Laurence-Moon-Biedl syndrome is an autosomal recessive disorder characterized by obesity, hypogenitalism, polydactyly, mental retardation and retinitis pigmentosa. Occasionally, this syndrome is accompanied by renal anomaly, nystagmus, cataract, syndactyly, microcephaly, oxycephaly... -
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- A Case of Laurence-Moon-Biedl Syndrome
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Kim SD, Kim YK, Kim JD
- KMID: 1949261
- J Korean Ophthalmol Soc.
- 1989 Aug;30(4):671-674.
Laurence-Moon-Biedl syndrome is a rare and autosomal recessive disorder characterized by obesity, hypogenitalism, polydactylism, mental retardation and retinitis pigmentosa. Occasionally, this syndrome is accompanied by nystagmus, cataract, syndactylism, microcephaly, oxycephaly... -
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- A Case of Laurence-Moon-Biedl Syndrome
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Chi NC
- KMID: 2122561
- J Korean Ophthalmol Soc.
- 1975 Mar;16(1):85-88.
A case of Laurence-Moon-Biedl Syndrome in 13-year-old Korean boy was reported with some clinical observation. Visual disturbance and night blindness were his chief complaints for about 3 years prior to... -
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