[Pierre Marie-Sainton cleidocranial dysplasia].

Abstract excerpt

The paper presents a family with hereditary transmitted Marie-Sainton dysplasia affecting the father and his both children. This is a rare syndrome presenting an autosomal pattern of inheritance, characterized by a generalized defect in both membranous and endochondral bone formation resulting in clavicular aplasia, delayed ossification of the fontanelles and the sutures of the skull and prolonged retention of...

Topics

Share this publication in a Topic to start or enrich a Post.

• Share to Cleidocranial Dysplasia
• Share to Core Binding Factor Alpha 1 Subunit