What is Acrocephalosyndactyly Syndrome type 5?
What is Acrocephalosyndactyly Syndrome type 5?
- Acrocephalosyndactyly Syndrome type 5: A rare genetic disorder where some of the skull bones fuse too early which affects the size and shape of the skull and face. Thumb and toe abnormalities are also present. There are three types of Pfeiffer syndrome with varying degrees of severity.
Acrocephalosyndactyly Syndrome type 5: Introduction
Types of Acrocephalosyndactyly Syndrome type 5:
Broader types of Acrocephalosyndactyly Syndrome type 5:
How serious is Acrocephalosyndactyly Syndrome type 5?
Complications of Acrocephalosyndactyly Syndrome type 5:
see complications of Acrocephalosyndactyly Syndrome type 5
What causes Acrocephalosyndactyly Syndrome type 5?
Causes of Acrocephalosyndactyly Syndrome type 5: see causes of Acrocephalosyndactyly Syndrome type 5
What are the symptoms of Acrocephalosyndactyly Syndrome type 5?
Symptoms of Acrocephalosyndactyly Syndrome type 5:
see symptoms of Acrocephalosyndactyly Syndrome type 5
Complications of Acrocephalosyndactyly Syndrome type 5:
see complications of Acrocephalosyndactyly Syndrome type 5
Acrocephalosyndactyly Syndrome type 5: Testing
Diagnostic testing: see tests for Acrocephalosyndactyly Syndrome type 5.
Misdiagnosis: see misdiagnosis and Acrocephalosyndactyly Syndrome type 5.
How is it treated?
Treatments for Acrocephalosyndactyly Syndrome type 5:
see treatments for Acrocephalosyndactyly Syndrome type 5
Name and Aliases of Acrocephalosyndactyly Syndrome type 5
Main name of condition: Acrocephalosyndactyly Syndrome type 5
Other names or spellings for Acrocephalosyndactyly Syndrome type 5:
Noack's syndrome, Pfeiffer syndrome
Source - Diseases Database