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Acrocephalosyndactyly type 3 (ACPS 3)

Acrocephalosyndactyly type 3 (ACPS 3): Introduction

Acrocephalosyndactyly type 3 (ACPS 3): A rare genetic disorder characterized by premature joining of certain skull bones during development which has an impact on the shape of the head and face. Features include brachycephaly, ear deformities as well as craniofacial, finger and bone abnormalities. More detailed information about the symptoms, causes, and treatments of Acrocephalosyndactyly type 3 (ACPS 3) is available below.

Symptoms of Acrocephalosyndactyly type 3 (ACPS 3)

Treatments for Acrocephalosyndactyly type 3 (ACPS 3)

  • Treatment varies depending on the type and severity of symptom that develop:
  • Surgery may be needed to correct defects or abnormalities e.g. undescended testes
  • Access to programs and services as required e.g. physical therapy, speech therapy, educational support, social, vocational and medical services
  • Various symptomatic and supportive measures as required
  • Genetic counseling and joining a support group is recommended
  • more treatments...»

Wrongly Diagnosed with Acrocephalosyndactyly type 3 (ACPS 3)?

Causes of Acrocephalosyndactyly type 3 (ACPS 3)

Read more about causes of Acrocephalosyndactyly type 3 (ACPS 3).

Less Common Symptoms of Acrocephalosyndactyly type 3 (ACPS 3)

Misdiagnosis and Acrocephalosyndactyly type 3 (ACPS 3)

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Acrocephalosyndactyly type 3 (ACPS 3): Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Acrocephalosyndactyly type 3 (ACPS 3): Animations

Prognosis for Acrocephalosyndactyly type 3 (ACPS 3)

Prognosis for Acrocephalosyndactyly type 3 (ACPS 3): The prognosis varies depending on the type and severity of symptoms that develop. Prompt diagnosis and appropriate treatment can improve prognosis and quality of life.

Statistics for Acrocephalosyndactyly type 3 (ACPS 3)

Acrocephalosyndactyly type 3 (ACPS 3): Broader Related Topics

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Definitions of Acrocephalosyndactyly type 3 (ACPS 3):

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Acrocephalosyndactyly type 3 (ACPS 3) as a "rare disease".
Source - Orphanet

Related Acrocephalosyndactyly type 3 (ACPS 3) Info

More information about Acrocephalosyndactyly type 3 (ACPS 3)

  1. Acrocephalosyndactyly type 3 (ACPS 3): Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Prognosis
 

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