Trevor disease
(Redirected from Dysplasia epiphysealis hemimelica)
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| Trevor disease | |
|---|---|
| Synonyms | Dysplasia epiphysealis hemimelica, Fairbank's disease |
| Pronounce | N/A |
| Specialty | Orthopedic surgery |
| Symptoms | Limb deformity, joint pain, limping |
| Complications | N/A |
| Onset | Childhood |
| Duration | Chronic |
| Types | N/A |
| Causes | Unknown |
| Risks | |
| Diagnosis | X-ray, MRI |
| Differential diagnosis | Osteochondroma, Multiple hereditary exostoses |
| Prevention | N/A |
| Treatment | Surgery |
| Medication | Pain management |
| Prognosis | Variable |
| Frequency | Rare |
| Deaths | N/A |
Trevor disease, also known as dysplasia epiphysealis hemimelica (DEH), is a rare congenital disorder characterized by the abnormal growth of cartilage on one side of the epiphysis of long bones. This condition typically affects the lower extremities, particularly the ankle and knee joints, and is often diagnosed in children and adolescents.
Presentation
Trevor disease manifests as an asymmetrical overgrowth of cartilage, leading to deformities and functional impairments. Common symptoms include:
- Pain and swelling in the affected joint
- Limited range of motion
- Limb length discrepancy
- Joint deformity
Diagnosis
The diagnosis of Trevor disease is primarily based on clinical examination and imaging studies. X-ray imaging is commonly used to identify the characteristic cartilaginous overgrowth. In some cases, MRI or CT scan may be employed to provide a more detailed assessment of the extent of the lesion.
Treatment
Treatment options for Trevor disease depend on the severity of the condition and the symptoms presented. They may include:
- Observation and regular monitoring for mild cases
- Surgical intervention to remove the abnormal cartilage and correct deformities
- Physical therapy to improve joint function and mobility
Prognosis
The prognosis for individuals with Trevor disease varies. Early diagnosis and appropriate treatment can lead to significant improvements in joint function and quality of life. However, some individuals may experience persistent symptoms or require multiple surgical procedures.
See also
This congenital disorder related article is a stub. You can help WikiMD by expanding it.
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Contributors: Prab R. Tumpati, MD