| Literature DB >> 30796325 |
Hitomi Shimizu1,2, Satoshi Watanabe1, Akira Kinoshita2, Hiroyuki Mishima2, Gen Nishimura3, Hiroyuki Moriuchi1, Koh-Ichiro Yoshiura2, Sumito Dateki4.
Abstract
Spondylocarpotarsal synostosis syndrome, a rare syndromic skeletal disorder characterized by disrupted vertebral segmentation with vertebral fusion, scoliosis, short stature, and carpal/tarsal synostosis, has been associated with biallelic truncating mutations in the filamin B gene or monoallelic mutations in the myosin heavy chain 3 gene. We herein report the case of a patient with a typical phenotype of spondylocarpotarsal synostosis syndrome who had a homozygous frameshift mutation in the refilin A gene (RFLNA) [c.241delC, p.(Leu81Cysfs*111)], which encodes one of the filamin-binding proteins. Refilins, filamins, and myosins play critical roles in forming perinuclear actin caps, which change the nuclear morphology during cell migration and differentiation. The present study implies that RFLNA is an additional causative gene for spondylocarpotarsal synostosis syndrome in humans and a defect in forming actin bundles and perinuclear actin caps may be a critical mechanism for the development of spondylocarpotarsal synostosis syndrome.Entities:
Mesh:
Substances:
Year: 2019 PMID: 30796325 DOI: 10.1038/s10038-019-0581-9
Source DB: PubMed Journal: J Hum Genet ISSN: 1434-5161 Impact factor: 3.172