Craniosynostoses

Craniosynostoses:
Due to mutation of FGFR2 gene  premature fusion of cranial suture with variable abnormalities of the hands and feet.
All autosomal dominant disorders

Apert’s syndrome:
• syndactyly of fingers and toes

Jackson-Weiss syndrome:

Crouzon’s disease:

We have not yet got to this page. We will eventually. Please contact us if you have something to contribute to it or sign up for our newsletter or like us on Facebook and Instagram or follow us on Twitter.

Page last updated: @ 9:32 pm

Sub Topics:

Comments are closed.