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dc.contributor.authorKose, G
dc.contributor.authorKayserili, H
dc.contributor.authorAka, N
dc.contributor.authorVural, ZT
dc.contributor.authorPeker, O
dc.contributor.authorKumru, P
dc.date.accessioned2021-03-03T15:22:10Z
dc.date.available2021-03-03T15:22:10Z
dc.date.issued2005
dc.identifier.citationKumru P., Aka N., Kose G., Vural Z., Peker O., Kayserili H., "Short rib polydactyly syndrome type 3 with absence of fibulae (Verma-Naumoff syndrome)", FETAL DIAGNOSIS AND THERAPY, cilt.20, sa.5, ss.410-414, 2005
dc.identifier.issn1015-3837
dc.identifier.otherav_3e8ef82d-e823-42bb-8ebb-2936b37a8815
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/45924
dc.identifier.urihttps://doi.org/10.1159/000086822
dc.description.abstractShort rib polydactyly syndrome (SRPS) is a group of skeletal dysplasias manifested by short-limb dwarfism, short ribs with thoracic dysplasia and polydactyly. SIRPS is an inherited autosomal-recessive disorder with different prenatal sonographic and postnatal clinical, histological and radiologic findings. SIRPS type 1 (Saidino-Noonan) and type 3 (Verma-Naumoff) are very similar and frequently get mixed. In this report, we present a case of SRPS with hydrops, thoracic hypoplasia, short limbs and postaxial polydactyly in a 27-week fetus. The visceral findings in the fetus including the central nervous system were normal. The karyotype was 46XY. The prenatal diagnosis was thought to be type 1 because of the absence of fibulae at ultrasonography. However, postmortem autopsy, histologic, and radiologic findings were reviewed and the diagnosis was type 3 SRPS because of absence of visceral anomalies, presence of fan-shaped iliac bones and short tubular bones with metaphyseal widening. We concluded that detailed ultrasonography performed in the prenatal period is very important in the diagnosis and differential diagnosis of SRPS. Copyright (c) 2005 S. Karger AG, Basel.
dc.language.isoeng
dc.subjectKadın Hastalıkları ve Doğum
dc.subjectCerrahi Tıp Bilimleri
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectKADIN HASTALIKLARI & DOĞUM
dc.titleShort rib polydactyly syndrome type 3 with absence of fibulae (Verma-Naumoff syndrome)
dc.typeMakale
dc.relation.journalFETAL DIAGNOSIS AND THERAPY
dc.contributor.department, ,
dc.identifier.volume20
dc.identifier.issue5
dc.identifier.startpage410
dc.identifier.endpage414
dc.contributor.firstauthorID173927


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