dysostosis

The same can said for individuals with Cleidocranial dysostosis.

The term mandibulofacial dysostosis is used to describe the clinical features.

When synostosis is abnormal it is a type of dysostosis.

First called "craniofacial dysostosis", the disorder was characterized by a number of clinical features.

Clinically, different features of the dysostosis are significant.

The collarbones are sometimes partly or completely absent in cleidocranial dysostosis.

Early and late surgery in craniofacial dysostosis - A longitudinal cephalometric study.

A dysostosis is a disorder of the development of bone, in particular affecting ossification.

This gait may be caused by cleidocranial dysostosis.

Spondylocostal dysostosis is a rare, heritable axial skeleton growth disorder.

Mutations in Cbfa1/Runx2 are associated with the disease Cleidocranial dysostosis.

Maxillofacial dysostosis is inherited as an autosomal dominant trait.

Mutations in this gene cause autosomal recessive spondylocostal dysostosis 1.

A second (distinct) form of maxillofacial dysostosis is believed to be inherited as an X-linked recessive trait.

Nager acrofacial dysostosis is a congenital anomaly syndrome.

Some cases resemble Jarcho-Levin syndrome or spondylocostal dysostosis.

They specified their condition as spondylocostal dysplasia, which has since become known as spondylocostal dysostosis.

Cleidocranial dysostosis is found among the South African Muslim population due to a Chinese man who was affected by this disease.

In the congenital disorder cleidocranial dysostosis, the anterior fontanelle never closes to form the bregma.

Crouzon disease (craniofacial dysostosis)

Cleidocranial dysostosis is a general skeletal condition named for the collarbone (cleido-) and cranium deformities which people with it often have.

In 1949, Adolphe Franceschetti and David Klein described the same condition on their own observations as mandibulofacial dysostosis.

Crouzon was the first to describe a condition he called "craniofacial dysostosis", which is a genetic branchial arch disorder that results in abnormal facial features.

Marie is also credited as the first to describe pulmonary hypertrophic osteoarthropathy, cleidocranial dysostosis and rhizomelic spondylosis.

Mutations in the MESP2 gene cause autosomal recessive Spondylocostal dysostosis type 2.