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dc.contributor.authorUludag, S
dc.contributor.authorAksoy, F
dc.contributor.authorBarbaros, M
dc.contributor.authorOcak, V
dc.contributor.authorTuysuz, B
dc.contributor.authorMadazli, R
dc.date.accessioned2021-03-03T19:42:08Z
dc.date.available2021-03-03T19:42:08Z
dc.date.issued2002
dc.identifier.citationMadazli R., Tuysuz B., Aksoy F., Barbaros M., Uludag S., Ocak V., "Prenatal diagnosis of arthrogryposis multiplex congenita with increased nuchal translucency but without any underlying fetal neurogenic or myogenic pathology", FETAL DIAGNOSIS AND THERAPY, cilt.17, sa.1, ss.29-33, 2002
dc.identifier.issn1015-3837
dc.identifier.othervv_1032021
dc.identifier.otherav_55f9abae-1f33-42c3-b3c5-801bcf2358fa
dc.identifier.urihttp://hdl.handle.net/20.500.12627/60718
dc.identifier.urihttps://doi.org/10.1159/000048002
dc.description.abstractArthrogryposis multiplex congenita is a general term for congenital multiple joint contractures, the aetiology of which is variable. Prenatal diagnosis is usually based on the detection of diminished fetal movements and joint contractures on ultrasound. There are also reports of early diagnosis of arthrogryposis in the first and early second trimester by detection of subcutaneous oedema. We report another case of arthrogryposis multiplex congenita with increased nuchal translucency and scoliosis diagnosed by ultrasonography at 15 weeks of gestation. The pregnancy was terminated at the request of the parents. Post-mortem examination revealed that it was not associated with fetal myopathy or neuropathy. Multiple joint contractures with increased nuchal translucency without any underlying fetal neurogenic and myogenic pathology may be a distinct form of arthrogryposis multiplex congenita. Copyright (C) 2002 S. Karger AG, Basel.
dc.language.isoeng
dc.subjectSağlık Bilimleri
dc.subjectKadın Hastalıkları ve Doğum
dc.subjectCerrahi Tıp Bilimleri
dc.subjectKADIN HASTALIKLARI & DOĞUM
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectTıp
dc.titlePrenatal diagnosis of arthrogryposis multiplex congenita with increased nuchal translucency but without any underlying fetal neurogenic or myogenic pathology
dc.typeMakale
dc.relation.journalFETAL DIAGNOSIS AND THERAPY
dc.contributor.department, ,
dc.identifier.volume17
dc.identifier.issue1
dc.identifier.startpage29
dc.identifier.endpage33
dc.contributor.firstauthorID9866


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