- A Case of LEOPARD Syndrome
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Lee HJ, Chung HJ, Cho YH, Chung KY
- KMID: 2302588
- Korean J Dermatol.
- 2005 Jul;43(7):949-952.
LEOPARD syndrome is an autosomal dominantly inherited multiple congenital anomaly syndrome with high penetrance and a markedly variable expression. LEOPARD is an acronym of lentigines, electrocardiographic conduction defects, ocular hypertelorism,... -
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- A Rare Case of Left Ventricular Noncompaction in LEOPARD Syndrome
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Kim K, Kang MG, Park HW, Koh JS, Park JR, Hwang SJ, Hwang JY
- KMID: 2407681
- J Cardiovasc Ultrasound.
- 2018 Mar;26(1):43-44.
- doi: 10.4250/jcu.2018.26.1.43
No abstract available. -
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- LEOPARD Syndrome with PTPN11 Gene Mutation Showing Six Cardinal Symptoms of LEOPARD
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Kim J, Kim MR, Kim HJ, Lee KA, Lee MG
- KMID: 2156671
- Ann Dermatol.
- 2011 May;23(2):232-235.
- doi: 10.5021/ad.2011.23.2.232
LEOPARD multiple congenital anomaly syndrome inherited in an autosomal dominant manner. LEOPARD is an acronym for Lentigines, Eletrocardiographic conduction defects, Ocular hypertelorism, Pulmonary valve stenosis, Abnormalities of the genitalia, Retardation... -
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- A Case of Leopard Syndrome Associated with Pure Gonadal Dysgenesis
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Lee ES, Ko SH, Chi JS, Hur M, Park HM
- KMID: 2076668
- Korean J Obstet Gynecol.
- 2002 Jul;45(7):1273-1276.
Leopard syndrome, a feature of a syndrome, is a acronym of Lentiginosis, Electrocardiographic conduction abnormalities, Ocular hypertelorism, Pulmonic stenosis, Abnormal genitalia, Retardation of growth, and Deafness. It is one of... -
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- A case of LEOPARD syndrome with cor triatriatum
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Lee SG, Lee SY, Im SH, Yoo KD, Baek SH, Kim CM, Choi GB
- KMID: 1833206
- Korean J Med.
- 2003 Jul;65(1):99-103.
The LEOPARD syndrome is an acronym and serves as a mnemonic for the features of this autosomal dominant syndrome : L - lentigines (multiple), E - electrocardiographic conduction abnormalities, O... -
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- A Case of Multiple Lentigines Syndrome
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Shin DY, Koo DW, Roh JY
- KMID: 2360368
- Ann Dermatol.
- 1997 Jul;9(3):219-223.
- doi: 10.5021/ad.1997.9.3.219
The multiple lentigines syndrome or LEOPARD syndrome is an autosomal dominantly inherited disorder with a variety of abnormalities and a familial occurrence. This syndrome is characterized by the presence of... -
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- A Case of Leopard Syndrome with Atypical Psychosis
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Lee DG, Kim JG
- KMID: 2340684
- J Korean Neuropsychiatr Assoc.
- 2002 May;41(3):563-570.
Leopard syndrome is a neurocutaneous syndrome which may affect a variety of organ systems in the embryological aspects. It presents lentigines, EKG abnormalities, ocular hypertelorism, pulmonary stenosis, abnormalities of genitalia,... -
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- LEOPARD Syndrome with PTPN11 Gene Mutation
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Kim JM, Mun J, Song M, Kim HS, Kim BS, Kim MB, Ko HC
- KMID: 1427410
- Korean J Dermatol.
- 2013 Aug;51(8):635-638.
LEOPARD syndrome is an autosomal dominant inherited disease with multiple congenital anomalies. LEOPARD is an acronym for Lentigines, Electrocardiographic conduction defects, Ocular hypertelorism, Pulmonary stenosis, Abnormalities of the genitalia, Retardation... -
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- The Management of Cardiovascular Abnormalities in Patient With LEOPARD Syndrome
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Lee KJ, Choi H, Choi WH, Kwon SU, Doh JH, Namgung J, Lee SY, Lee WR
- KMID: 2225178
- Korean Circ J.
- 2010 Jul;40(7):339-342.
- doi: 10.4070/kcj.2010.40.7.339
LEOPARD syndrome (LS) is a rare hereditary disorder in Asian countries. This syndrome consists of multiple systemic abnormalities. In particular, characteristic cardiovascular effects in LS may include variable clinical manifestations... -
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- A Case of Multiple Lentigines Syndrome
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Park JH, Lee CY, Kim DH, Kim KH
- KMID: 1679140
- Korean J Dermatol.
- 1985 Feb;23(1):100-104.
We report a case of multiple leatiginea syndrome in an 8 year old boy. He had numeroua lentigines acattered over his face, trunk, buttock and thlghe, and eome larger black... -
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- Syndromic Hearing Loss in Association with PTPN11-Related Disorder: The Experience of Cochlear Implantation in a Child with LEOPARD Syndrome
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Chu HS, Chung HS, Ko MH, Kim HJ, Ki CS, Chung WH, Cho YS, Hong SH
- KMID: 2278484
- Clin Exp Otorhinolaryngol.
- 2013 Jun;6(2):99-102.
Hearing loss (HL) is one of the most frequent clinical manifestations of patients who suffer with multi-systemic genetic disorders. HL in association with other physical stigmata is referred to as... -
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- A Case of Multiple Lentigines Syndrome
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Paik SA, Kook HI
- KMID: 1854799
- Korean J Dermatol.
- 1978 Apr;16(2):131-136.
Multiple lentigines syndrome is characterized by the presence of numerous dark brown macules on the skin but not mucous surfaces and known also by the mnemvnic "LEOPARD syndrome" are, besides... -
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- A Case of Multiple Lentigines Sydrome with a Family History of Multiple Lentigines
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Kim SJ, Seo PS, Yoon NH, Park SD
- KMID: 1605845
- Korean J Dermatol.
- 2004 Dec;42(12):1581-1584.
Multiple lentigines syndrome is an autosomal dominant disorder of variable penetrance and expressivity. LEOPARD has been used to describe the main features of the syndrome, including lentigines, electrocardiographic abnormalities, ocular... -
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- A case of multiple lentigines syndrome
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Lee MW, Choi JH, Lee SC, Sung KJ, Koh JK
- KMID: 1693788
- Korean J Dermatol.
- 1993 Oct;31(5):780-783.
Supernunmerary nipple is a developmental anomaly occuring alon, the course of the embryological milk lines. This entity has receieved little attention in the dermatologic literature and has been confused with... -
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