FAQs of Infantile Cortical HyperostosisHow will I know if my children will be affected with Infantile Cortical Hyperostosis?
With advanced genetic techniques, it is possible to predict if your child will be affected by any genetic condition. But since Infantile Cortical Hyperostosis is a condition of unknown cause, genetic mapping is not always the answer. This together with the fact that the disease is mild and does not pose a threat to life makes this process irrelevant.
Which doctor should I see in case my child has several soft tissue swellings?
A pediatrician, orthopedic specialist or a dental surgeon are the doctors who will be able to diagnose and offer further advice about this condition
My child has been diagnosed as having Infantile Cortical Hyperostosis. Should I be worried?
No. Infantile Cortical Hyperostosis is a relatively mild condition and so far no fatalities have been reported. Therefore, there is no need to worry as such, but make sure that your child has regular check ups.
What are the complications of Infantile Cortical Hyperostosis?
Complication are extremely rare and include deformities of the involved bones, inequalities in limb-length.
What other conditions mimic Infantile Cortical Hyperostosis?
Differential diagnosis include
Importance of BreastFeeding
Infantile Cortical Hyperostosis
Insulin Delivery Devices
Internet Addiction Disorder
Irritable Bowel Syndrome
Infantile cortical hyperostosis is a disease affecting the bone and adjacent tissues of infants. The cortex of the affected bones (usually, the jawbones, collarbones, and the bones in the arms and legs) thickens and the surrounding tissue swells. The disease usually appears before the baby is six months old and disappears during childhood.
Join this online group on infantile cortical hyperstosis to contact doctors and meet other parents of children with this condition.