نمایش مختصر رکورد

dc.contributor.authorNasimi, Maryamen_US
dc.contributor.authorAzizpour, Arghavanen_US
dc.contributor.authorAbedini, Robabehen_US
dc.contributor.authorGhanadan, Alirezaen_US
dc.date.accessioned1399-07-09T06:22:44Zfa_IR
dc.date.accessioned2020-09-30T06:22:44Z
dc.date.available1399-07-09T06:22:44Zfa_IR
dc.date.available2020-09-30T06:22:44Z
dc.date.issued2017-04-01en_US
dc.date.issued1396-01-12fa_IR
dc.date.submitted2019-12-22en_US
dc.date.submitted1398-10-01fa_IR
dc.identifier.citationNasimi, Maryam, Azizpour, Arghavan, Abedini, Robabeh, Ghanadan, Alireza. (2017). Unilateral generalized morphea: A case report and literature review. Iranian Journal of Dermatology, 20(2), 59-62.en_US
dc.identifier.issn2717-0721
dc.identifier.urihttp://iranjd.ir/article_99391.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/301118
dc.description.abstractMorphea is an autoimmune connective tissue disease of the dermis and subcutaneous fat characterized by sclerosis due to excessive collagen deposition. Morphea is classified into different subtypes based on clinical and histological characteristics of cutaneous lesions. An extremely rare subtype of morphea is termed unilateral generalized morphea (UGM). UGM is characterized by indurated plaques on dermatomes of the trunk or back with a sharp midline demarcation line. Ipsilateral limbs may also be affected. There is still debate on whether this type of morphea should be considered as a distinct type or a presentation of linear morphea. Here we report the case of an 8-year-old boy with this type of morphea.en_US
dc.format.extent632
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoen_US
dc.publisherIranian Society of Dermatologyen_US
dc.relation.ispartofIranian Journal of Dermatologyen_US
dc.titleUnilateral generalized morphea: A case report and literature reviewen_US
dc.typeTexten_US
dc.typeCase Reporten_US
dc.citation.volume20
dc.citation.issue2
dc.citation.spage59
dc.citation.epage62


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