{Reference Type}: Case Reports
{Title}: Identification of two novel MYH3 variants causing different phenotypes in prenatal diagnosis.
{Author}: Yang Y;Zhang W;Wang H;
{Journal}: Prenat Diagn
{Volume}: 43
{Issue}: 11
{Year}: 2023 10 13
{Factor}: 3.242
{DOI}: 10.1002/pd.6440
{Abstract}: The MYH3 gene encodes the embryonic myosin heavy chain, which is crucial for the skeletal and muscular development. The MYH3 variants are associated with distal arthrogryposis type 2A (Freeman-Sheldon syndrome), distal arthrogryposis type 2B3 (Sheldon-Hall syndrome), CPSFS1A (Contractures, pterygia, and spondylocarpostarsal fusion syndrome 1A) and CPSFS1B, which have some shared characteristics and great variability of clinical phenotypes. In this study, we report two novel MYH3 missense variants c.1024T>G (p.Phe342Val) and c.3872A>C (p.Gln1291Pro), demonstrating different phenotypes in the prenatal setting. This study expands the spectrum of MYH3 variants and supports the domain-specific genotype-phenotype correlation of MYH3.