LTBP3 and Acromicric dysplasia: The mutation of the LTBP3 gene results in structural and functional changes of the related proteins, leading to the development of 3 distinct disorders: acromicric dysplasia (OMIM 102,370), dental abnormalities and short stature (OMIM 601,216), and gelephysical dysplasia 3 (GPHYSD3) (OMIM 617,809).[8–10] The above mutation explained our patients’ range of clinical manifestations, all of whom presented with skeletal abnormalities, fetal limb shortening, maternal and elder daughter’s short stature, as well as shortened hands and fingers.