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dc.contributor.authorMunira S. Mahmudova, Surayyo M. Shukurdjanova, Nigora B. Nuritdinova-
dc.date.accessioned2022-12-27T18:43:54Z-
dc.date.available2022-12-27T18:43:54Z-
dc.date.issued2022-
dc.identifier.issn2689-1026-
dc.identifier.urihttp://repository.tma.uz/xmlui/handle/1/5572-
dc.description.abstractThe article presents a clinical case of congenital arteriovenous dysplasia – Parkes Weber syndrome of the lower extremities. The features of its clinical picture and the difficulties of diagnosis are described. It is emphasized that Parkes Weber syndrome is a rare congenital disease of the vascular system, in some cases with the absence of its typical clinical manifestations and combined with other pathologies of the veinsen_US
dc.language.isoenen_US
dc.publisherThe American Journal of Medical Sciences and Pharmaceutical Researchen_US
dc.relation.ispartofseriesVolume 04 Issue 12-2022;-
dc.subjectParkes Weber syndrome, venous angiodysplasiaen_US
dc.titleCOMPLICATIONS OF PARKES WEBER SYNDROMEen_US
dc.typeArticleen_US
Appears in Collections:Thesis, Articles

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