Achondroplasia - Treatments

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What can be done for patients with achondroplasia?

Children and adults with achondroplasia can lead normal lives provided they receive attentive, informed care by their physicians and parents. Considerations in monitoring children with achondroplasia include careful measurements of growth (length/height and weight) and head circumference using curves specially standardized for those with achondroplasia. Knowledgeable pediatric care and periodic orthopedic and neurologic examinations are critical.

When special problems complicate achondroplasia, prompt and expert intervention is important. For example:

  • The foramen magnum (the large opening under the skull) may need to be surgically enlarged in cases of severe narrowing (stenosis) and compression of the spinal cord. When this opening is too narrow, the blood vessels and nerves are compressed, which can lead to central apnea (loss of breathing control). This is responsible for the risk of sudden death in infants (SIDS) with achondroplasia. The risk of sudden death for infants with achondroplasia is 2% to 5%.
  • The back of individuals with achondroplasia can develop a marked sway (lordosis) to the lower back while abnormalities in the mid-back may cause a small hump (kyphosis) in infancy and compression of the spinal cord in adolescence. The spinal cord compression can require surgery to decompress it. Spinal stenosis is the most common medical complication of achondroplasia seen in adulthood.
  • Orthopedic procedures may be performed for lengthening of the limb bones and correction of bowed legs (usually after full growth has been achieved).
  • Surgery (lumbar laminectomy) is also indicated when spinal stenosis (narrowing) causes symptoms, which tends to be evident in young adults.
  • Disproportion between the brain and the base of the skull can sometimes result in hydrocephalus ("water on the brain") which needs to be promptly detected and treated by placement of a shunt to drain the excess fluid.
  • The large head with achondroplasia increases the chance of bleeding within the baby's head during vaginal delivery. This should be taken into account in planning the birth and postnatal care, and Cesarean delivery (C-section) may be recommended for a fetus with achondroplasia. The brainstem (which contains a center for controlling respiration) may be compressed in achondroplasia and contribute to abnormal breathing.
  • Pregnant women with achondroplasia should have their babies delivered by cesarean section, due to their characteristically small pelvis, and high risk of birth related trauma.
  • Middle ear infections (otitis media) are frequent and can lead to mild to moderate hearing loss. Therefore, ear infections should be readily suspected and promptly and fully treated with antibiotics and/or ear tubes.
  • Dental crowding is also common. Teeth should be straightened and, if necessary, removed to alleviate this problem.
  • Control of obesity is essential, and obesity can be a significant problem in people with achondroplasia. The excessive weight gain usually occurs during childhood. When obesity is present, the back and joint problems that are characteristic of this condition worsen in severity. The child with achondroplasia must not be allowed to become overweight. Adults with achondroplasia should also monitor and control their weight.
  • Treatment with human growth hormone, which is still considered experimental, has been preliminarily reported to increase the growth rate after treatment, but studies have not yet demonstrated that adult height is increased by this treatment.
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Comment from: s rehan, 19-24 Male (Caregiver) Published: May 06

According to my experience growth hormone is responsible for achieving maximum height. I have some relatives who are suffering from this disease (achondroplasia) and they achieved their maximum height as they had growth hormone injections every month, 6 doses.

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