Fibular hemimelia is the complete absence of the fibula. Sometimes there is a shortening of it. Being rare (0.3 per 10,000 live births) it is the most common of the congenital absences that can affect the long bones of the extremities.
Its cause is not known with certainty, and it is probably due to a vascular disorder that affects the development of the fibula. No hereditary or toxic factors have been identified. It can be accompanied by other malformations or bone absences in the same or in the other limb.
A series of signs can indicate that we are facing a fibular hemimelia:
Broadly speaking, we have three options:
Treatment will depend on the degree of involvement and can be orthopedic or surgical.
The most important thing is that the treatment be as early as possible and appropriate because these children have problems standing or walking and we must ensure that they do so when it corresponds to them in their evolutionary development.
The treatment must be multidisciplinary, that is, with different specialists:
This medical team will develop a plan to help your child get up and stay up, walk, and play like other children. We must seek the maximum normality possible.
The affectation is partial and unimportant, there is not much difference in the length of both legs. In those cases, it is enough for the children to use a special shoe or an insole . But most children need surgery.
Basically we have two technical options:
Only in very extreme cases is there no choice but to partially amputate the leg and fit a prosthesis.
Essential of course:
With this name we refer to the complete congenital absence of the fibula. Sometimes there is a shortening of it.
The treatment must be multidisciplinary, that is, with different specialists: child orthopedic surgeon, physiotherapist and orthopedic technician.
Treatment will depend on the degree of involvement and can be orthopedic or surgical. Only in very extreme cases is there no choice but to partially amputate the leg and fit a prosthesis.
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