Searchable abstracts of presentations at key conferences in endocrinology

ea0077p115 | Reproductive Endocrinology | SFEBES2021

Disentangling Turner syndrome and Leri-Weill Dyschondrosteosis; the importance of genetic assessment in the management of Turner Syndrome

Hanington Lucy , Shears Debbie , Turner Helen

Leri-Weill Dyschondrosteosis (LWD) is a skeletal dysplasia resulting in short stature and mesomelic limb-shortening; Madelung deformity of the wrist is often present. Mutation or deletion of the SHOX gene is the underlying cause of LWD. SHOX plays a role in regulating proliferation and maturation of chondrocytes. It is located in the pseudoautosomal region of the sex chromosomes (Xp22.3/Yp11.3); males and females usually have 2 functioning copies. Turner synd...