Craniosynostosis autosomal dominant

Overview

Craniosynostosis autosomal dominant: A dominantly inherited defect involving the fusion of one or more bones in the skull before it has finished growing which affects the head size and shape and can affect the growth of the brain. The defect is often associated with other conditions. Symptoms are determined by which skull bones are prematurely fused.

Symptoms

The list of signs and symptoms mentioned in various sources for Craniosynostosis autosomal dominant includes the 2 symptoms listed below: * Abnormal head shape * Dysmorphic facial features

Diagnosis

The phrase "signs of Craniosynostosis autosomal dominant" should, strictly speaking, refer only to those signs and symptoms of Craniosynostosis autosomal dominant that are not readily apparent to the patient. The word "symptoms of Craniosynostosis autosomal dominant" is the more general meaning; see symptoms of Craniosynostosis autosomal dominant. The signs and symptom information on this page attempts to provide a list of some possible signs and symptoms of Craniosynostosis autosomal dominant. This medical information about signs and symptoms for Craniosynostosis autosomal dominant has been gathered from various sources, may not be fully accurate, and may not be the full list of Craniosynostosis autosomal dominant signs or Craniosynostosis autosomal dominant symptoms. Furthermore, signs and symptoms of Craniosynostosis autosomal dominant may vary on an individual basis for each patient. Only your doctor can provide adequate diagnosis of any signs or symptoms and whether they are indeed Craniosynostosis autosomal dominant symptoms.