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dc.contributor.authorYagi, Hiroko
dc.contributor.authorNishimura, Gen
dc.contributor.authorTakagi, Masaki
dc.contributor.authorHasegawa, Yukihiro
dc.contributor.authorKayserili, Hulya
dc.date.accessioned2021-03-04T18:13:54Z
dc.date.available2021-03-04T18:13:54Z
dc.date.issued2015
dc.identifier.citationYagi H., Takagi M., Hasegawa Y., Kayserili H., Nishimura G., "Sclerosteosis (craniotubular hyperostosis-syndactyly) with complex hyperphalangy of the index finger", PEDIATRIC RADIOLOGY, cilt.45, ss.1239-1243, 2015
dc.identifier.issn0301-0449
dc.identifier.otherav_899ec969-b8c8-4a70-8823-dfe2d39ef747
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/93322
dc.identifier.urihttps://doi.org/10.1007/s00247-015-3292-1
dc.description.abstractWe report a 4-year-old boy with sclerosteosis associated with severe digital dysostosis. The initial medical consultation was prompted by bilateral, asymmetrical syndactyly of the index and middle fingers. The left index finger had complicated phalangeal anomalies: hyperphalangy (supernumerary phalanx distal to the middle phalanx) and hypoplasia with bracket epiphyses of the proximal and middle phalanges. Development of facial nerve palsy, hearing impairment and generalized osteosclerosis had occurred between 3 years and 4 years of age, with the subsequent identification of a homozygous SOST mutation. Bilateral second and third fingers syndactyly associated with abnormal patterning of the same fingers should be considered prodromal signs of sclerosteosis.
dc.language.isoeng
dc.subjectNükleer Tıp
dc.subjectTıp
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectRADYOLOJİ, NÜKLEER TIP ve MEDİKAL GÖRÜNTÜLEME
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectPEDİATRİ
dc.titleSclerosteosis (craniotubular hyperostosis-syndactyly) with complex hyperphalangy of the index finger
dc.typeMakale
dc.relation.journalPEDIATRIC RADIOLOGY
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume45
dc.identifier.issue8
dc.identifier.startpage1239
dc.identifier.endpage1243
dc.contributor.firstauthorID223187


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