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Andersson, K., Dahllöf, G., Lindahl, K., Kindmark, A., Grigelioniene, G., Åström, E., et al. (2017) Mutations in COL1A1 and COL1A2 and Dental Aberrations in Children and Adolescents with Osteogenesis Imperfecta—A Retrospective Cohort Study. PLOS ONE, 12, e0176466.
https://doi.org/10.1371/journal.pone.0176466

has been cited by the following article:

• TITLE: Case Report and Clinical Management of a Case of Osteogenesis Imperfecta Detected in the Prenatal Period

  AUTHORS: Amina Chaieb, Oumayma Ben Rejeb, Samar Knaz, Yasmine Ben Ali, Syrine Chelly, Safia Ernez, Mouna Derouiche

  KEYWORDS: Osteogenesis Imperfecta, Ultrasound Screening, Antenatal Diagnosis

  JOURNAL NAME: Open Journal of Obstetrics and Gynecology, Vol.14 No.7, July 10, 2024

  ABSTRACT: Osteogenesis imperfecta is a hereditary disease characterized by bone fragility due to a defect in type I collagen synthesis. The diagnosis is typically suspected based on suggestive ultrasound findings and confirmed through genetic studies. We present a case of osteogenesis imperfecta suspected during obstetrical ultrasound at 19 weeks’ gestation, which was later confirmed radiographically through computed tomography. Due to the severity of the condition, therapeutic termination of pregnancy was indicated.