Prenatal Cases Reflect the Complexity of the <i>COL1A1/2</i> Associated Osteogenesis Imperfecta

Prenatal Cases Reflect the Complexity of the <i>COL1A1/2</i> Associated Osteogenesis Imperfecta

Introduction: Osteogenesis imperfecta (OI) is a rare mendelian skeletal dysplasia with autosomal dominant or recessive inheritance pattern, and almost the most common primary osteoporosis in prenatal settings. The diversity of clinical presentation and genetic etiology in prenatal OI cases presents...

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Bibliographic Details
Main Authors: Kai Yang, Yan Liu, Jue Wu, Jing Zhang, Hua-ying Hu, You-sheng Yan, Wen-qi Chen, Shu-fa Yang, Li-juan Sun, Yong-qing Sun, Qing-qing Wu, Cheng-hong Yin
Format: Article
Language:English
Published: MDPI AG 2022-09-01
Series:Genes
Subjects:
Osteogenesis imperfecta
<i>COL1A1</i>
<i>COL1A2</i>
<i>CANT1</i>
<i>RMRP</i>
Online Access:https://www.mdpi.com/2073-4425/13/9/1578

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https://www.mdpi.com/2073-4425/13/9/1578

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