Kohler disease is a rare condition that affects the foot bones in children. It is also known as navicular osteochondrosis or Kohler bone disease. It was first described by Alban Kohler, a German radiologist, in 1908. The disease occurs when the blood supply to the navicular bone is disrupted, causing the bone to become damaged and eventually collapse. In this article, we will discuss the symptoms, causes, diagnosis, and treatment options for Kohler disease.
The symptoms of Kohler disease typically appear in children between the ages of 3 and 5. The most common symptoms include:
The exact cause of Kohler disease is unknown. However, it is believed to be caused by a disruption of blood flow to the navicular bone. This disruption can be caused by a variety of factors, including:
To diagnose Kohler disease, a doctor will perform a physical exam and review the child's medical history. They may also order imaging tests, such as X-rays or an MRI, to look for signs of bone damage or collapse. Other tests that may be performed include:
The treatment for Kohler disease depends on the severity of the condition. In mild cases, the condition may resolve on its own over time. However, in more severe cases, treatment may be necessary. Treatment options include:
There are no known ways to prevent Kohler disease. However, parents can take steps to reduce their child's risk of developing the condition, such as:
Kohler disease is a rare condition that affects the foot bones in children. The symptoms include pain, swelling, and difficulty walking. The exact cause of the condition is unknown, but it is believed to be related to a disruption in blood flow to the navicular bone. Treatment options include rest, immobilization, and physical therapy. With proper treatment, most children with Kohler disease can recover fully and resume normal activities.
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