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A Case of Sturge-Weber Syndrome

Choi JS, Yi KP, Hong KY

  • KMID: 2336515
  • J Korean Ophthalmol Soc.
  • 1989 Jun;30(3):459-464.
Sturge-Weber syndrome is a congenital disorder characterized by facial nevus flammeus along the distribution of the trigeminal nerve, ipsilatal leptomeningioma, buphthalmos, and choroidal angioma. The Authors experienced a case of...
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A Case of Sturge-Weber Syndrome

Lee WH, Oh SJ, Jho HD, Yoo YR, Kim NK, Chung HY

  • KMID: 2068148
  • J Korean Neurosurg Soc.
  • 1983 Dec;12(4):715-719.
Sturge-Weber syndrome was rare. But reported from 1860. We present a typical case of Sturge-Weber syndrome in a child and discussed the symptoms, signs, and pathological finding of various examinations...
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Sturge-Weber Syndrome with Congenital Ocular Anomaly

Chung IH, Kim MH

  • KMID: 2205190
  • J Korean Ophthalmol Soc.
  • 1995 Dec;36(12):2266-2270.
Sturge-Weber syndrome is a rare congenital anomaly which includes facial port-wine stains with ipsilateral intracranial, hemangioma, ipsilateral choroidal hemangioma, and congenital glaucoma. The syndrome is thought to result from dysmorphogenesis...
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Anesthesia for a Sturge-Weber Syndrome Patient with Severe Facial Hemangioma: A case report

Chung KD, Son YS, Hong SH, Cho HS

Sturge-Weber syndrome is characterized by congenital skin angiomas throughout the facio-trigeminal region, which can cause difficulty in airway management in the case of general anesthesia. The problems with this syndrome...
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Atypical Sturge-Weber Syndrome: A case report

Kim YJ, Kim C, Ahn JK, Bang IK, Lee SM

  • KMID: 2178761
  • J Korean Acad Rehabil Med.
  • 2002 Dec;26(6):811-814.
Sturge-Weber syndrome is a congenital neurocutaneous disorder of the vessels of the face, the leptomeninges and the brain. Clinically SWS consists of symptoms and signs including a facial nevus (port-wine...
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A Case of Sturge-Weber Syndrome

Park JT, Jang GH, Lee JK, Lee KE, Oh JH

  • KMID: 1699101
  • J Korean Pediatr Soc.
  • 1983 Aug;26(8):823-828.
No abstract available.
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A Case of Sturge-Weber Syndrome

Jo JS, Chao MC, Moon DS, Cho KS, Cho CD

  • KMID: 1676557
  • J Korean Pediatr Soc.
  • 1986 Apr;29(4):103-108.
No abstract available.
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An Infantile Case of Sturge-Weber Syndrome in Association with Klippel-Trenaunay-Weber Syndrome and Phakomatosis Pigmentovascularis

Lee CW, Choi DY, Oh YG, Yoon HS, Kim JD

Sturge-Weber syndrome can be associated with facial port-wine stains and intracranial calcification, and concurrent Klippel-Trenaunay-Weber syndrome has been reported. Klippel-Trenaunay-Weber syndrome is a rare congenital mesodermal phakomatosis characterized by cutaneous...
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A Case of Acquired Cleft Lip and Nasal Deformity in a Patient with Sturge-Weber Syndrome

Yoo SA

  • KMID: 1668202
  • J Korean Pediatr Soc.
  • 1980 Nov;23(11):962-964.
A case of Sturge-Weber Syndrome is presented in a male neonate with severe gangrenous ulcerative stomatitis involving the angiomatous skin lesion and leaving sequele of cleft lip and nasal disfiguration.
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A Case of Sturge-Weber Syndrome

Kim SY, Kim HS, Kim MS, Park SY, Shin DH

  • KMID: 1668581
  • J Korean Pediatr Soc.
  • 1981 Nov;24(11):1111-1115.
No abstract available.
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Malnutrition-Related Fulminant Type 1 Diabetes in a Patient with Sturge-Weber Syndrome

Oh JS, Yu J

Fulminant type 1 diabetes is a subtype of idiopathic type 1 diabetes and is characterized by a short duration of symptom onset and an absence of anti-islet autoantibodies. It has...
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MR Imaging in sturge-weber syndrome: one case report

Hong HS, Kim DH, Chung MC, Kwon KH, Kim KJ

One 6-month-old of Sturge-Weber syndrome examined with MR imaging and CT scan was reported. Both techniques well demonstrated unilateral cortical atrophy. In the region of parenchymal volume loss, MR better...
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MR Findings of Sturge-Weber Syndrome Without Facial Nevus: Two Cases Report

Juhng SK, Choi SS, Noh BS, Kim CG, Won JJ

  • KMID: 2102251
  • J Korean Radiol Soc.
  • 1994 Mar;30(3):417-420.
PURPOSE: We reported the CT and MR findings of 2 cases with Sturge-Weber syndrome which were not accompanied by facial nevi. MATERIALS AND METHODS: They were examined with both CT and MR...
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Clinical Features and Surgical Outcomes of Sturge-Weber Syndrome with Glaucoma

Park JH, Lim SH, Cha SC

PURPOSE: To report clinical manifestations including neurocutaneous and ocular findings and to evaluate outcomes of trabeculectomy in patients with Sturge-Weber syndrome. METHODS: The medical records of 10 eyes of 8 glaucoma...
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Sturge-Weber Syndrome

Chen L, Wu J, Xu M, Chen N, Yang Y

  • KMID: 2383266
  • Ann Dermatol.
  • 2011 Nov;23(4):551-553.
Sturge-Weber syndrome (SWS) is a neurocutaneous syndrome, characterized by the association of facial port-wine hemangiomas in the trigeminal nerve distribution area, with vascular malformation(s) of the brain (leptomeningeal angioma) with...
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Clinical Experience of Treatment in a Case of Sturge-Weber Syndrome with Bilateral Glaucoma

Kim JW, Park CH, Lee CH

  • KMID: 2123467
  • J Korean Ophthalmol Soc.
  • 1996 May;37(5):908-912.
Sturge-Weber syndrome is a rare congenital anomaly characterized by angiomatosis of face, eye and leptomeninges and nevus flammeus is distributed along the trigminal nerve in face, often accompanying congenital glaucoma....
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A Case of Sturge-Weber Syndrome

Chung I, Jang SG, Lew HM

  • KMID: 2204801
  • J Korean Ophthalmol Soc.
  • 1986 Aug;27(4):723-728.
Sturge- Weber syndrome is a congenital disorder and marked by cutaneous angiomatosis along the distribution of the trigeminal nerve, ipsilateral leptomeningeal angiomatosis, bupthalmos and choroidal angioma. A 22 year old...
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A Case of Klippel-Trenaunay Syndrome Combinded with Sturge-Weber Syndrome

Kim MY, Lee SY, Kim NY, Lee SJ, Kim WD, Cho SM, Lee DS, Kim DK, Choi SM

  • KMID: 1607045
  • J Korean Pediatr Soc.
  • 2003 Sep;46(9):909-912.
Klippel-Trenaunay syndrome is a rare mesodermal phakomatosis characterized by cutaneous haemangiomata(usually unilateral and involving an extremity), venous varicosities and osseous and soft tissue hypertrophy, of the affected limb. Sturge-Weber syndrome,...
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A case of glaucoma associated with Sturge-Weber syndrome and Nevus of Ota

Lee H, Choi SS, Kim SS, Hong YJ

The Sturge-Weber syndrome consists of a unilateral port-wine hemangioma of the skin along the trigeminal distribution and is accompanied by an ipsilateral leptomeningeal angioma. Glaucoma is present in approximately half...
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A Case of Incomplete form cf Sturge-Weber Syndrome

Nam SH, Rim CS, Lee KC, Kim HY, Chi JG

  • KMID: 2138542
  • J Korean Neurosurg Soc.
  • 1985 Jun;14(2):451-456.
Sturge-Weber syndrome is a neurocutaneous syndrome characterized by portwine nevus of the face with angiomatosis of the ipsilateral cerebral leptomeninges and extensive calcification in the underlying cerebral cortex. Associated features...
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