| Literature DB >> 34144233 |
John L Fowlkes1, Kathryn M Thrailkill2, R Clay Bunn2.
Abstract
The RASopathies comprise an ever-growing number of clinical syndromes resulting from germline mutations in components of the RAS/MAPK signaling pathway. While multiple organs and tissues may be affected by these mutations, this review will focus on how these mutations specifically impact the musculoskeletal system. Herein, we review the genetics and musculoskeletal phenotypes of these syndromes in humans. We discuss how mutations in the RASopathy syndromes have been studied in translational mouse models. Finally, we discuss how signaling molecules within the RAS/MAPK pathway are involved in normal and abnormal bone biology in the context of osteoblasts, osteoclasts and chondrocytes.Entities:
Keywords: Capillary malformation-arteriovenous malformation syndrome; Cardio-facio-cutaneous syndrome; Costello syndrome; Legius syndrome; Neurofibromatosis type 1; Noonan syndrome; RAS/MAPK pathway
Year: 2021 PMID: 34144233 DOI: 10.1016/j.bone.2021.116060
Source DB: PubMed Journal: Bone ISSN: 1873-2763 Impact factor: 4.398