Article
The third case of TNFRSF11A-associated dysosteosclerosis with a mutation producing elongating proteins.
Journal of human genetics - 1 Apr 2021
Xue Jing-Yi, Wang Zheng, Smithson Sarah F, Burren Christine P, Matsumoto Naomichi, Nishimura Gen, Ikegawa Shiro, Guo Long
Abstract excerpt
Dysosteosclerosis (DOS) is a distinct form of sclerosing bone disease characterized by platyspondyly and progressive osteosclerosis. DOS is genetically heterogeneous. Three causal genes, SLC29A3, CSF1R, and TNFRSF11A are reported. TNFRSF11A-associated DOS has been identified in two patients; however, TNFRSF11A is also a causal gene for osteopetrosis, autosomal recessive 7 (OP-AR7). Whole-exome sequencing in a...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
