- A Case of Piebaldism Associated with Strabismus and Torticollis
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Nam KS, Lee HJ, Whang KU, Kim YK
- KMID: 2230724
- Korean J Dermatol.
- 1996 Feb;34(1):151-154.
Piebaldism is a rare autosomal dominant genetic disorder characterized by localized and stationary hypomelanosis of skin and hair secondary to an absence of melanocytes in the involved skin. Depigmentation in... -
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- Piebaldism: a case report
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Hwang SM, Ahn SK, Lee WS, Yoo MS, Choi EH
- KMID: 644965
- J Korean Med Sci.
- 1996 Jun;11(3):285-288.
- doi: 10.3346/jkms.1996.11.3.285
We report a familial case of piebaldism affecting a 33-year-old man and his 3-month-old son. Typical skin findings, white forelock and amelanotic white macules containing hyperpigmented macules, were characteristically presented... -
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- Four Generations of Piebaldism
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Park HS, Jang SJ, Lee YS, Chun DK
- KMID: 2086605
- Korean J Dermatol.
- 2002 Oct;40(10):1273-1276.
Piebaldism is an uncommon autosomal dominant genetic disorder. It is characterized by amelanotic macules or patches, usually containing some hyperpigmented or normopigmented macules, of the central portion of the forehead,... -
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- Piebaldism Associated with Café-au-lait Macules and Intertriginous Freckling: A Case Report and Review of the Literature
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Akarsu S, İlknur T, Avcı C, Fetil E
- KMID: 2456236
- Ann Dermatol.
- 2019 Oct;31(5):567-570.
- doi: 10.5021/ad.2019.31.5.567
We present 9-year-old fraternal twins from a family with piebaldism, having congenital depigmented macules and meeting the diagnostic criteria for neurofibromatosis type 1 (NF1) due to the multiple café-au-lait macules... -
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- A Case of Piebaldism Treated by Combination Therapy with Suction Blister Epidermal Graft and the Alexandrite Laser
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Choe HC, Kim MY, Park HJ, Byun DG, Park CJ
- KMID: 2303061
- Korean J Dermatol.
- 2002 Nov;40(11):1389-1392.
Piebaldism is a rare, autosomal dominant inherited disorder, characterized by inborn hypopigmented skin and hair. It is characterized by stable leukoderma with white forelock and vitiligo like amelanotic macules usually... -
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- Piebaldism with Neurofibromatosis Type I: A Familial Case
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Park SY, Kim HJ, Ahn SK
- KMID: 2171670
- Ann Dermatol.
- 2014 Apr;26(2):264-266.
- doi: 10.5021/ad.2014.26.2.264
No abstract available. -
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- Novel KIT Missense Mutation P665S in a Chinese Piebaldism Family
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Zheng Y, Liu F, Yang Y, Liang Y
- KMID: 2395195
- Ann Dermatol.
- 2017 Dec;29(6):801-803.
- doi: 10.5021/ad.2017.29.6.801
No abstract available. -
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- Congenital Deafness associated with Piebaldism
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Kim SM, Lee SM, Kim EK
- KMID: 1891573
- Korean J Dermatol.
- 1996 Apr;34(2):304-308.
Woolf syndrome is characterized by piebaldism and congenital deafness. Facial features of Waardenburg syndrome are absent and the parents and siblings are unaffected. We report herein a case of Woolf... -
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- Clinical Study of 11 Cases of Piebaldism in Koreans
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Whang SW, Kim SM, Hann SK
- KMID: 1568183
- Korean J Dermatol.
- 2000 Jun;38(6):721-728.
BACKGROUND: Piebaldism is an uncommon congenital disease inherited in autosomal dominant pattern. It is characterized by stable leukoderma with white forelock and vitiligo-like amelanotic macules usually containing a few normally... -
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- Poliosis Circumscripta Associated with Halo Nevus of the Scalp
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Jang HC, Kim HJ, Hyun DN, Lee SW, Chung H
- KMID: 1891788
- Korean J Dermatol.
- 2006 Oct;44(10):1250-1252.
Poliosis circumscripta describes a localized patch of white hair due to deficiency of melanin in the hair follicles. It is a feature of various conditions such as piebaldism, Vogt-Koyanagi-Harada syndrome,... -
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- The Features of Tyrosinase Expressions in Pigmentary Disorders Using TTA
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Lee YK, Kim YH, Kim KH
- KMID: 2302073
- Korean J Dermatol.
- 2008 Mar;46(3):325-333.
BACKGROUND: Tyrosinase is the critical enzyme in melanin synthesis. DOPA staining has been used as a standard assay for detecting tyrosinase activity, but it exhibits several limitations. Tyramide based tyrosinase... -
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- A Case of Chediak-Higashi Syndrome
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Han HK, Koo HM, Chung SK
- KMID: 2123361
- J Korean Ophthalmol Soc.
- 1995 May;36(5):879-884.
Chediak-Higashi syndrome is a rare autosomal recessive disease characterized by partial oculocutaneous albinism, photophobia, nystagmus, immunodeficiency with increased susceptibility to bacterial and viral infection. We experienced a 2-year old boy... -
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