- Two Cases of Coccygeal Polypoid Eccrine Nevi Presenting as Skin Tags
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Park MY, Lee ES
- KMID: 2156517
- Ann Dermatol.
- 2009 Nov;21(4):440-442.
- doi: 10.5021/ad.2009.21.4.440
An eccrine nevus is a rare hamartoma characterized by an increase in the number or size of eccrine glands. Eccrine nevi usually present as localized hyperhidrosis and are not associated... -
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- Clinical Study on Neonatal Skin
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Lee SY, Oh CH, Cinn YW, Kim SN
- KMID: 2085668
- Korean J Dermatol.
- 1989 Dec;27(6):680-685.
The present study was carried out to investigate the incidence and clinical features of neonatal skin abnormalities. Six hundred eight neonates were examined in Korea University Guro Hospital from May... -
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- A Study on Tests of Skin Safety and Inhibition of Atopic Dermatitis Using a StoneTouch(R) Infrared Scanner in a Mouse Model
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Lim YY, Kim HM, Jang WS, Seo SH, Ahn HH, Kim MN, Kim BJ
- KMID: 2088178
- Korean J Dermatol.
- 2011 Mar;49(3):217-226.
BACKGROUND: Atopic dermatitis is a chronic inflammatory skin disease. It is caused by immunological abnormalities, abnormalities of the skin barrier, environmental factors and genetic factors. Atopic dermatitis destroys the skin... -
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- An autopsy case of Adams-Oliver syndrome
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Jun SY, Khang SK, Park SH
- KMID: 1730652
- J Korean Med Sci.
- 2000 Aug;15(4):482-484.
- doi: 10.3346/jkms.2000.15.4.482
We report an autopsy case of a male fetus with Adams-Oliver syndrome. His mother was a healthy, 31-year-old woman and her family and past histories were unremarkable. Therapeutic termination was... -
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- A Case of Goltz Syndrome
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Lee DH, Park CH, Park JM, Park SB, Kim HS, Ryoo YW, Lee KS, Lee HJ
- KMID: 1606829
- J Korean Pediatr Soc.
- 2003 Jun;46(6):606-609.
Goltz syndrome(focal dermal hypoplasia) is a rare disorder characterized by ectodermal and mesodermal dysplasia described in 1962 by Goltz. In Korea, one case of Goltz syndrome was reported in 1994.... -
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- Epicanthoplasty Using Y-M Plasty
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Kim DH, Yoon SW, Kim CH
- KMID: 2266931
- Arch Aesthetic Plast Surg.
- 2011 Jun;17(2):112-118.
Lots of Koreans have relatively thick skin, small palpebral fissures and unfolded eyelids with a prominent epicanthal fold. Various methods have been developed to correct epicanthal fold. However, excessive or... -
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- Two Cases of Nevus Comedonicus
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Sohn KA, Woo JS, Chi JH
- KMID: 1663961
- Korean J Dermatol.
- 1970 Jan;8(1):63-66.
Nevus comedonicus is a rare skin abnormality characterized by a unilateral and usually linear distribution of groups of comedones, Histologically, local epidermal invagination and keratin material plugging in invaginated pouch... -
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- A Case of Post-Herpetic Nevoid Comedones
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Seo JK, Jeong KH, Shin MK
- KMID: 2456672
- Ann Dermatol.
- 2019 Aug;31(Suppl):S36-S38.
- doi: 10.5021/ad.2019.31.S.S36
No abstract available. -
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- A Case of Post-Herpetic Nevoid Comedones
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Seo JK, Jeong KH, Shin MK
- KMID: 2456645
- Ann Dermatol.
- 2019 Aug;31(Suppl 1):S36-S38.
- doi: 10.5021/ad.2019.31.S.S36
No abstract available. -
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- Ehlers-Danlos Syndrome in a Newborn Mistaken for Edwards Syndrome
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Kim SK, An JW, Lee SH, Oh YK
- KMID: 2409124
- Perinatology.
- 2017 Dec;28(4):156-161.
- doi: 10.14734/PN.2017.28.4.156
The Ehlers-Danlos syndrome (EDS) is an inherited connective tissue disorder with special characteristics such as joint hypermobility, tissue fragility and skin abnormalities. The recently classification divide six subtypes. Dermatosparaxis types... -
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- A giant retroperitoneal lymphangioma in a patient with neurofibromatosis type 1
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Kim JH, Kim MO, Choi YJ, Han HY, Park KS, Cho BS, Kang DW
- KMID: 2096649
- J Korean Surg Soc.
- 2011 Jun;80(Suppl 1):S43-S46.
- doi: 10.4174/jkss.2011.80.Suppl1.S43
Neurofibromatosis type 1 (NF-1) is a genetically inherited disorder that may cause skin abnormalities and tumors that form on nerve tissues. These tumors can be small or large and can... -
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- Dermatomyositis in an Allogeneic Stem Cell Transplant Recipient with Graft-Versus-Host Disease
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Kim Y, Kang SW, Jo DY, Park CK, Song KS, Kim JM, Kim J
- KMID: 2128479
- Korean J Med.
- 2014 Apr;86(4):523-527.
Dermatomyositis (DM) is an autoimmune disease characterized by subacute-onset proximal symmetric muscle weakness, skin abnormalities, and muscle inflammation. Descriptions of DM as a complication of chronic graft-versus-host disease (cGVHD) are... -
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- A Case of Malignant Peripheral Nerve Sheath Tumor of the Neck Associated with Neurofibromatosis Type I
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Kim DH, Lee SS, Lee SH, Lee DW
- KMID: 1490041
- Korean J Otorhinolaryngol-Head Neck Surg.
- 2010 Oct;53(10):657-660.
- doi: 10.3342/kjorl-hns.2010.53.10.657
Neurofibromatosis is an autosomal dominant hereditary disorder characterized by skin abnormalities such as cafe au-lait spots, and soft tissue legion such as generalized subcutaneous neurofibroma. Malignant peripheral nerve sheath tumor... -
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- Outcome of ultrasonographic imaging in infants with sacral dimple
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Choi JH, Lee T, Kwon HH, You SK, Kang JW
- KMID: 2414248
- Korean J Pediatr.
- 2018 Jun;61(6):194-199.
- doi: 10.3345/kjp.2018.61.6.194
PURPOSE: Sacral dimples are a common cutaneous anomaly in infants. Spine ultrasonography (USG) is an effective and safe screening tool for patients with a sacral dimple. The aim of this... -
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- A Case of Visual Loss Following Injection of Poly-(L)-Lactic Acid Filler into the Right Forehead
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Cho YW, Chung IY, Park JM, Yoo JM, Kim SJ, Seo SW, Han YS
- KMID: 2338870
- J Korean Ophthalmol Soc.
- 2014 Aug;55(8):1253-1256.
PURPOSE: We report a case of visual loss after the injection of poly-L-lactic acid filler into the right forehead area for cosmetic purposes. CASE SUMMARY: A 46-year-old female patient visited our... -
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- Two Cases of Tuberous Sclerosis Patients with Renal Anomaly
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Moon SH, Choi HJ, Yun UD, Yang DK, Woo YS, Chang KY, Jee SR, Oh IH, Kim SE, Kim KH
- KMID: 2254506
- Korean J Nephrol.
- 2001 Jan;20(1):137-142.
Tuberous sclerosis is a rare disease, which occurs sporadically or hereditarily and is recognized by its neurological and dermatological manifestations and may be accompanied with renal anomalies. The classical triad... -
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