Larsen syndrome is a rare congenital anomaly that causes abnormal development of bones and joints. This is usually evident from birth. Larsen syndrome is a rare disorder. The actual incidence is approximately 1/100,000.
Symptoms of Larsen Syndrome
Symptoms of Larsen syndrome can include facial features, abnormalities of the fingers or feet, curvature of the spine, short stature, joint problems and, in some cases, mental retardation.
How Can Families Recognize?
Families should consult a doctor if they notice significant joint or bone abnormalities in their children after birth. The diagnosis can usually be made by physical examination and radiologic imaging.
Do they have types?
There are different types of Larsen syndrome and the severity and prevalence of symptoms can vary. But usually the main symptoms are similar.
Larsen Syndrome Treatment
Treatment usually focuses on symptom management. This may include correcting bone and joint abnormalities through surgical interventions. Physical therapy and rehabilitation may also be used.
Do I Need Supportive Devices, Therapy?
In some cases, patients may need orthotics or prostheses to correct or support joint or bone abnormalities. Physical therapy and treatment can help increase range of motion and improve muscle strength.
In Which Situations and When Is Surgery Performed?
Surgical intervention is often necessary for Larsen syndrome, especially if there are serious conditions such as spinal curvature or joint abnormalities.
What you need to know about Larsen Syndrome
Larsen syndrome is a rare congenital anomaly and treatment is usually focused on symptom management. Early diagnosis and treatment are important and long-term follow-up may be required.