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dc.contributor.authorSu, Ozlem
dc.contributor.authorULUSAL, Hande Arda
dc.contributor.authorOnsun, NAHİDE
dc.contributor.authorOZKAYA, Dilek Biyik
dc.date.accessioned2019-10-05T14:30:35Z
dc.date.available2019-10-05T14:30:35Z
dc.date.issued2011-09-01
dc.identifier10.1007/s00404-006-0172-9
dc.identifier.citationSu O., ULUSAL H. A. , OZKAYA D. B. , Onsun N., -Linear Nevus Sebaceous Syndrome in a Child With Ocular Choristoma and Hemimegalencephaly-, TURKDERM-ARCHIVES OF THE TURKISH DERMATOLOGY AND VENEROLOGY, cilt.45, ss.155-157, 2011
dc.identifier.urihttps://hdl.handle.net/20.500.12645/4081
dc.identifier.urihttps://www.journalagent.com/z4/vi.asp?pdir=turkderm&plng=tur&un=TURKDERM-85688
dc.description.abstractLinear nevus sebaceous syndrome (LNSS) is a phakomatosis, associated with a variety of developmental abnormalities of ocular, nervous, skeletal, cardiovascular and urogenital systems. In LNSS, choristomas and colobomas are frequently seen signs, but complex choristomas are rare. We describe a case of a 3-year-old boy with a yellow alopecic plaque on his scalp, face and neck as well as a mass in the episcleral region since birth. He also had epileptic seizures since one year old. Histopathological examination of episcleral specimen revealed choristoma. Magnetic resonance imaging of the brain identified hemimegalencephaly, hemicerebral atrophy, and lateral ventricular enlargement (Turkderm 2011; 45: 155-7)
dc.language.isoen
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectLinear Nevus Sebaceous Syndrome
dc.titleLinear Nevus Sebaceous Syndrome in a Child With Ocular Choristoma and Hemimegalencephaly
dc.typeArticle
local.avesis.response3951
local.article.journalnameArchives of gynecology and obstetrics
dc.identifier.wosWOS:000295572800009
dc.identifier.scopus80053212006
dc.identifier.doi10.4274/turkderm.85688
local.publication.isinternational1


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