Ellis-van Creveld syndrome

Information, Symptoms, Treatments and Resources

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Definition

Ellis-van Creveld syndrome is a rare genetic disorder that affects bone growth. The main features include dwarfism with shortening of the parts of the limbs farthest from the middle of the body.

Alternative Names

Chondroectodermal dysplasia; EVC

Causes, incidence, and risk factors

Ellis-van Creveld is inherited as an autosomal recessive trait. It results from defects in one of two Ellis van Creveld syndrome genes (EVC and EVC2). The two genes lie next to each other on chromosome 4. It is unclear how this unusual arrangement affects the presentation of the syndrome.

The severity of the disease varies from person to person. The highest rate of the condition is seen among the Old Order Amish population of Lancaster County, Pennsylvania.

Symptoms

Signs and tests

  • Skeletal x-ray may show fusion of wrist bones, cone shaped fingertips
  • Echocardiogram
  • Urinalysis
  • Chest x-ray showing short ribs
  • Ultrasound may locate an undescended testicle
  • Genetic testing may be available for mutations in the EVC gene

Treatment

Treatment depends on which body system is affected and how severe the problem is. The condition itself is not treatable, but many of the complications can be treated.

Expectations (prognosis)

The outcome depends on which body system is involved and to what extent that body system is involved.

Complications

Calling your health care provider

Call your health care provider if your child has symptoms of this syndrome. If you have a family history of Ellis-van Creveld syndrome and your child has any of the above symptoms, a visit to your health care provider is appropriate.

Prevention

Genetic counseling is recommended for prospective parents with any family history of Ellis-van Creveld syndrome.

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Review date: June 24, 2007
Reviewed by: Chad Haldeman-Englert, MD, Division of Human Genetics, Children's Hospitalof Philadelphia, Philadelphia, PA. Review provided by VeriMed HealthcareNetwork.

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