Infrequent association of two rare diseases: amniotic band syndrome and osteogenesis imperfecta

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dc.authorid0000-0003-0903-6520en_US
dc.authorid0000-0001-5556-1866en_US
dc.authorid0000-0002-9809-0977en_US
dc.authorid0000-0001-9978-9694en_US
dc.authorid0000-0001-8093-5583en_US
dc.contributor.authorDarakci, Savaş Mert
dc.contributor.authorErtuğrul, Sabahattin
dc.contributor.authorYılmaz, Sibel Tanrıverdi
dc.contributor.authorÜnal, Edip
dc.contributor.authorYolbaş, İlyas
dc.contributor.authorDeğer, İbrahim
dc.date.accessioned2023-01-11T10:54:11Z
dc.date.available2023-01-11T10:54:11Z
dc.date.issued2021en_US
dc.departmentDicle Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Çocuk Sağlığı ve Hastalıkları Ana Bilim Dalıen_US
dc.description.abstractObjectives: Amniotic band syndrome and osteogenesis imperfecta are two distinct diseases that develop due to structural defects of the collagen protein. In our paper, we report the concurrence of these two diseases rarely seen in the newborn period. Case presentation: A female infant born at 33rd gestational week was found to have constrictive bands in her right lower extremity and flexion contractures in distal joints of lower and upper extremities due to amniotic bands in postnatal physical examination. While being treated for respiratory difficulty, she was diagnosed with osteogenesis imperfecta and treated with bisphosphonates upon being found to suffer bilateral humeral fractures on the sixth day of life. She received respiratory support with mechanical ventilation due to respiratory tract complications related to osteogenesis imperfecta and died on the 384th day of life. Conclusions: One should bear in mind that other collagen tissue diseases may accompany the amniotic band syndrome; this possibility should be definitely pursued if clinical suspicion exists.en_US
dc.identifier.citationDarakci, S.M., Ertuğrul, S., Yılmaz, S.T., Ünal, E., Yolbaş, İ. ve Değer, İ. (2021). Infrequent association of two rare diseases: amniotic band syndrome and osteogenesis imperfecta. Case Reports in Perinatal Medicine, 10(1)en_US
dc.identifier.doi10.1515/crpm-2021-0035
dc.identifier.issn2192-8932
dc.identifier.issn2192-8959
dc.identifier.issue1en_US
dc.identifier.urihttps://www.degruyter.com/document/doi/10.1515/crpm-2021-0035/html
dc.identifier.urihttps://hdl.handle.net/11468/11194
dc.identifier.volume10en_US
dc.identifier.wosWOS:000734489100005
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.institutionauthorErtuğrul, Sabahattin
dc.institutionauthorYılmaz, Sibel Tanrıverdi
dc.institutionauthorÜnal, Edip
dc.institutionauthorYolbaş, İlyas
dc.institutionauthorDeğer, İbrahim
dc.language.isoenen_US
dc.publisherWalter de Gruyter GMBHen_US
dc.relation.ispartofCase Reports in Perinatal Medicine
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAmniotic band syndromeen_US
dc.subjectCongenital clubfooten_US
dc.subjectHypotoniaen_US
dc.subjectMicrognathismen_US
dc.subjectOsteogenesis imperfectaen_US
dc.titleInfrequent association of two rare diseases: amniotic band syndrome and osteogenesis imperfectaen_US
dc.titleInfrequent association of two rare diseases: amniotic band syndrome and osteogenesis imperfecta
dc.typeArticleen_US

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