Craniodiaphyseal dysplasia, autosomal dominant

Craniodiaphyseal dysplasia, autosomal dominant: Introduction

Craniodiaphyseal dysplasia, autosomal dominant: A rare inherited syndrome characterized mainly by bone overgrowth and sclerosis or hardening which affects mainly the skull but other bones are often involved as well. Craniotubular dysplasia is a similar condition but involves more severe hyperostosis and sclerosis. More detailed information about the symptoms, causes, and treatments of Craniodiaphyseal dysplasia, autosomal dominant is available below.

Symptoms of Craniodiaphyseal dysplasia, autosomal dominant

• Severe hearing loss
• Facial diplegia
• Sclerosis of diaphyses
• Asymmetric hyperostosis of long bones
• Metaphyseal modeling defects
• more symptoms...»

See full list of 16 symptoms of Craniodiaphyseal dysplasia, autosomal dominant

Causes of Craniodiaphyseal dysplasia, autosomal dominant

Read more about causes of Craniodiaphyseal dysplasia, autosomal dominant.

Craniodiaphyseal dysplasia, autosomal dominant: Broader Related Topics

• Head conditions
• Musculoskeletal conditions
• Bone or skeletal conditions
• more types...»

Types of Craniodiaphyseal dysplasia, autosomal dominant

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