De Novo Heterozygous Mutation in FGFR2 Causing Type II Pfeiffer Syndrome

<div>(a) CT scan of the head showing marked cloverleaf deformity with lateral ventricle dilatation. (b) Three-dimensional craniofacial reconstruct computed tomography of the skull (AP and lateral) demonstrating early closure and overlapping of all the cranial sutures with cloverleaf deformation.</div>

Case Reports in Genetics

fig3

Figure 3

Figure 3: De Novo Heterozygous Mutation in FGFR2 Causing Type II Pfeiffer Syndrome 