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What is Acrocephalosyndactyly II?

What is Acrocephalosyndactyly II?

  • Acrocephalosyndactyly II: A rare inherited disorder characterized primarily by premature closure of skull bones, fusion of fingers and toes and eye and face abnormalities.

Acrocephalosyndactyly II: Introduction

Types of Acrocephalosyndactyly II:

Broader types of Acrocephalosyndactyly II:

How serious is Acrocephalosyndactyly II?

Complications of Acrocephalosyndactyly II: see complications of Acrocephalosyndactyly II

What causes Acrocephalosyndactyly II?

Causes of Acrocephalosyndactyly II: see causes of Acrocephalosyndactyly II

What are the symptoms of Acrocephalosyndactyly II?

Symptoms of Acrocephalosyndactyly II: see symptoms of Acrocephalosyndactyly II

Complications of Acrocephalosyndactyly II: see complications of Acrocephalosyndactyly II

Acrocephalosyndactyly II: Testing

Misdiagnosis: see misdiagnosis and Acrocephalosyndactyly II.

How is it treated?

Doctors and Medical Specialists for Acrocephalosyndactyly II: Medical Geneticist ; see also doctors and medical specialists for Acrocephalosyndactyly II.
Treatments for Acrocephalosyndactyly II: see treatments for Acrocephalosyndactyly II

Name and Aliases of Acrocephalosyndactyly II

Main name of condition: Acrocephalosyndactyly II

Other names or spellings for Acrocephalosyndactyly II:

ACS II, Apert-Crouzon syndrome, Apert atypical, cephalosyndactyly, Vogt cephalodactyly

Acrocephalosyndactyly II: Related Conditions

Research the causes of these diseases that are similar to, or related to, Acrocephalosyndactyly II:

 

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