- A Possible Case of Epidermolysis Bullosa Simplex with Mottled Pigmentation
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Juhn BJ, Lee MH
- KMID: 1863735
- Korean J Dermatol.
- 2000 Mar;38(3):413-416.
Epidermolysis bullosa simplex with mottled pigmentation (EBS-MP) is a rare subtype of EBS and characterized by blistering of the skin, mottled pigmentation, and palmoplantar hyperkeratosis. We report a 3-year-old boy with mottled... -
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- A Case of Koebner Variant of Epidermolysis Bullosa Simplex
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Lim SJ, Jung SP, Lim IS, Lee DK, Yoo BH
- KMID: 1838675
- J Korean Soc Neonatol.
- 2001 May;8(1):166-170.
Epidermolysis bullosa simplex (EBS), characterized by a cleavage plane through basal keratinocytes, is caused by a mutation of the genes encoding keratin 5 and 14. It is often regarded as... -
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- A Case of Epidermolysis Bullosa Simplex ( Dowling - Meara Type )
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Chang SN, Kim SC
- KMID: 2085755
- Korean J Dermatol.
- 1994 Aug;32(4):735-739.
The Dowling-Meara type of epidermolysis bullosa simplex(EBS) is genetic disease that is transmitted as an autosomal dominant trait and is charscterized clinically by pherpetiform clustering of blisters and palmo-plantar keratoderma.... -
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- Dominant Dystrophic Epidermolysis Bullosa
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Lee HJ, Jung YJ, Kim JH, Hong H, Choi EH
- KMID: 2247681
- Korean J Dermatol.
- 2010 Oct;48(10):889-892.
Dystrophic epidermolysis bullosa is a rare, chronic non-inflammatory bullous disease with a hereditary pattern of occurrence, and this disease easily produces bullae that heal with scarring and milium formation. A... -
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- The Use of Cultured Allogenic Keratinocyte Grafting in a Patient with Epidermolysis Bullosa Simplex
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Shin KC, Park BY, Kim HK, Kim WS, Bae TH
- KMID: 2171881
- Ann Dermatol.
- 2011 Dec;23(Suppl 3):S393-S397.
- doi: 10.5021/ad.2011.23.S3.S393
Epidermolysis bullosa (EB) is a rare genetic disease that is known for continuous skin blistering caused by minor trauma. The skin blisters and bullae that develop often cause skin defects.... -
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- A Case of Weber-Cockayne Epidermolysis Bullosa Simplex - Ultrastructural Findings
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Lee IJ, Kim SC
- KMID: 2303516
- Korean J Dermatol.
- 1997 Feb;35(1):214-219.
Epidermolysis bullosa simplex (EBS) is a group of autosomal dominantly inherited genetic disorders characterized by blistering due to mechanical- stress-induced degeneration of basal epiderrnal cells. Recently, it was discovered that... -
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- Two Cases of Epidermolysis Bullosa Simplex
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Byun JH, Kook HI
- KMID: 1677788
- Korean J Dermatol.
- 1978 Dec;16(6):507-511.
Epidermolysis Bullosa Simplex is characterized by autosomal dominant rnheritance, and chronic noninflammatory conditions in which the clinical lesions, erosion, blisters usually result from relatively minor mechanical trauma to the skin,... -
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- A Case of Epidermolysis Bullosa Simplex
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Choi DY, Son SJ, Shin S
- KMID: 2085533
- Korean J Dermatol.
- 1981 Feb;19(1):117-121.
Epidermolysis bullosa aimplex is a dominantly inherited syndrome characterized by the dissolution of the basal epidermal cells with mechanical stress. A 23 year-old man developed recurrent bullous eruptions with pain... -
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- Two Cases of Epidermolysis Bullosa Simplex (Dowling-Meara Type)
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Lee HJ, Kwon SB, Lee SJ, Chung SL, Kim HM, Kim DJ
- KMID: 2303254
- Korean J Dermatol.
- 2000 Jul;38(7):955-960.
The Dowling-Meara type of epidermolysis bullosa simplex is a rare genodermatosis transmitted by autosomal dominant pattern. It starts during the first 3 months of life and is characterized by generalized... -
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- Epidermolysis bullosa simplex (Dowling-Meara type) associated with pyloric atresia and congenital urologic abnormalities
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Kim DK, Kim SC, Chang SN, Kim SY
- KMID: 711768
- Yonsei Med J.
- 2000 Jun;41(3):411-415.
- doi: 10.3349/ymj.2000.41.3.411
We report a case of epidermolysis bullosa simplex, Dowling-Meara type (EBS-DM), which was associated with congenital pyloric atresia (PA) and various urologic abnormalities, a diagnosis confirmed by immunofluorescence mapping... -
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- Incontinentia Pigmenti: Report of 4 Cases in a Family
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Cho KE, Bark WH, Oh JI, Woo TH
- KMID: 2039202
- Korean J Dermatol.
- 1970 Jul;8(2):73-77.
Four cases of incontinentia pigmenti (Bloch-Sulzberger type) in a mother and three her daughter were presented and literatures were reviewed. In all three daughters vesicles appeared on toes at three... -
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- A Case of Epidermolysis Bullosa Simplex (Other Generalized Type)
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Ko DY, Ha SM, Jeon SY, Kim DC, Song KH, Kim KH
- KMID: 2247246
- Korean J Dermatol.
- 2013 Mar;51(3):219-222.
The other generalized type of epidermolysis bullosa simplex (EBS) is a genetic blistering skin disease, caused by a mutation of the genes encoding keratin 5 and 14. EBS starts at... -
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- Weber-Cockayne Type Epidermolysis Bullosa Simplex Resulting from a Novel Mutation (c. 608T>C) in the Keratin 5 Gene
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Cho JW, Ryu HW, Kim SA, Nakano H, Lee KS
- KMID: 2264870
- Ann Dermatol.
- 2014 Dec;26(6):739-742.
- doi: 10.5021/ad.2014.26.6.739
Epidermolysis bullosa simplex (EBS), an inherited genetic disorder, is most often caused by a dominant-negative mutation in either the keratin 5 (KRT5) or the keratin 14 (KRT14) gene. These keratin... -
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