Congenital partial dislocation of hip, unilateral digital illustration

Congenital partial dislocation of hip, unilateral Save


ICD-10 code: Q65.3

Chapter: Congenital malformations, deformations and chromosomal abnormalities

Congenital Partial Dislocation of Hip, Unilateral: Causes, Symptoms, and Treatment

Congenital partial dislocation of hip, unilateral is a condition that affects infants at birth and causes the hip joint to be partially dislocated. The condition affects only one hip joint and can cause pain, discomfort, and difficulty in walking as the child grows.

The causes of congenital partial dislocation of hip, unilateral are not entirely clear, but some factors such as genetics, family history, and environmental factors may contribute to the development of the condition. However, the exact cause of the condition is still unknown.

Symptoms

The symptoms of congenital partial dislocation of hip, unilateral may vary from mild to severe. Some of the common symptoms of the condition include:

  1. One leg appearing shorter than the other
  2. Limited movement of the affected hip joint
  3. Difficulty in walking or limping
  4. Pain or discomfort in the affected hip or groin area
Treatment

The treatment for congenital partial dislocation of hip, unilateral depends on the severity of the condition. Mild cases may not require any treatment, but more severe cases may require medical intervention.

The most common treatment for congenital partial dislocation of hip, unilateral is the use of a Pavlik harness. This is a special device that is used to hold the hip joint in place and encourage proper alignment. The harness is usually worn for several months, and regular check-ups with a doctor are necessary to monitor the progress of the treatment.

In severe cases, surgery may be required to correct the alignment of the hip joint. Surgery is usually done before the child is 2 years old to prevent any long-term complications.

Conclusion

Congenital partial dislocation of hip, unilateral is a condition that can affect infants at birth. Early diagnosis and treatment are essential to prevent long-term complications. If you notice any symptoms of the condition in your child, it is important to seek medical attention immediately.