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Acrocephalosyndactyly type 3 (ACPS 3)

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)

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Premature closure of coronal sutures
Premature closure of lambdoid sutures
Abnormal cranial development
Premature closing of skull bones
Premature closing of metopic sutures
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See full list of 43 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
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Wrongly Diagnosed with Acrocephalosyndactyly type 3 (ACPS 3)?

Misdiagnosis of Acrocephalosyndactyly type 3 (ACPS 3)

Causes of Acrocephalosyndactyly type 3 (ACPS 3)

Less Common Symptoms of Acrocephalosyndactyly type 3 (ACPS 3)

See full list of 14 occasional 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:

Arthritis & Joint Health Specialists (Rheumatology):
- Rheumatology (Joint Health)
- Pediatric Rheumatology (Child Joint Health)
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Other doctor, physician and specialist research services:

Acrocephalosyndactyly type 3 (ACPS 3): Animations

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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.

More about prognosis of Acrocephalosyndactyly type 3 (ACPS 3)

Statistics for Acrocephalosyndactyly type 3 (ACPS 3)

Acrocephalosyndactyly type 3 (ACPS 3): Broader Related Topics

Types of Acrocephalosyndactyly type 3 (ACPS 3)

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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

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