Diastematomyelia digital illustration

Diastematomyelia Save


ICD-10 code: Q06.2

Disease category: Q06: Other congenital malformations of spinal cord

Understanding Diastematomyelia

Diastematomyelia is a rare congenital disorder that affects the spinal cord. It occurs when the spinal cord splits into two separate parts, resulting in a condition where the spinal cord is divided into two halves. This division often occurs in the lower back region, and it is typically accompanied by a bony or fibrous septum that further separates the two halves of the spinal cord.

Diastematomyelia is more commonly found in females than males, and it is often associated with other spinal abnormalities. These additional abnormalities may include spinal cord tethering, spinal curvature (scoliosis), or the presence of extra bony structures called spurs. The exact cause of diastematomyelia is still unknown, but researchers believe that it may be related to disruptions in embryonic development during the early stages of pregnancy.

Diastematomyelia can lead to various symptoms, depending on the severity and location of the split. Some individuals may experience no noticeable symptoms, while others may develop neurological problems such as muscle weakness, numbness, or difficulty walking. In severe cases, it can even lead to paralysis or loss of bladder and bowel control.

  1. Types of Diastematomyelia:
    • Complete Diastematomyelia: In this type, the spinal cord is completely split into two distinct halves.
    • Incomplete Diastematomyelia: Here, the split may be partial, with the two halves partially fused together.

Diagnosis of diastematomyelia typically involves a combination of physical examination, medical history review, and imaging tests such as X-rays, magnetic resonance imaging (MRI), or computed tomography (CT) scans. Early detection is crucial to prevent potential complications and allow for appropriate management.

Although there is no specific treatment for diastematomyelia itself, individuals with this condition may require medical intervention to manage associated symptoms or complications. This may involve physical therapy to improve muscle strength and mobility, pain management strategies, or surgical procedures to address spinal abnormalities or relieve pressure on the spinal cord.

In conclusion, diastematomyelia is a rare spinal cord disorder that involves the splitting of the spinal cord into two halves. It can cause various neurological symptoms and often coexists with other spinal abnormalities. Early diagnosis and appropriate management are essential for optimizing outcomes for individuals with this condition.

Treatment of Diastematomyelia:

Treatment Options for Diastematomyelia

Diastematomyelia is a rare congenital spinal cord anomaly that affects the development of the spinal cord. It is characterized by the presence of a split in the spinal cord, which can lead to various neurological symptoms. While there is currently no cure for diastematomyelia, there are several treatment options available to manage symptoms an...

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