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Leg lengthening and shortening | University of Maryland Medical Center

Leg lengthening and shortening | University of Maryland Medical Center

Leg lengthening and shorteningToggle: English / Spanish


Leg lengthening and shortening are types of surgery to treat some children who have legs of unequal lengths.

These procedures may:
Lengthen an abnormally short legShorten an abnormally long legLimit growth of a normal leg to allow a short leg to grow to a matching length
Alternative Names

Epiphysiodesis; Epiphyseal arrest; Correction of unequal bone length; Bone lengthening; Bone shortening; Femoral lengthening; Femoral shortening



This series of treatments involves several surgeries, a long recovery period, and a number of risks. However,? it can add up to 6 inches of length to a leg.

The child will be under general anesthesia. This means the child is asleep and pain-free during surgery.
The bone to be lengthened is cut.Metal pins or screws are placed through the skin and into the bone. Pins are placed above and below the cut in the bone. Stitches are used to close the wound.? A metal device? is attached to the pins in the bone. It will be used later to very slowly (over months) pull the cut bone apart. This creates a space between the ends of the cut bone that will fill in with new bone.
When? the leg has reached the desired length and has healed, another surgery is? done to remove the pins.


This is a complicated surgery that can produce a very precise degree of correction.

While the child is under general anesthesia:
The bone to be shortened is cut. A section of bone is removed.The ends of the cut bone will be joined. A metal plate with screws or a nail down the center of the bone is placed across the bone to hold it in place during healing.

Bone growth takes place at the growth plates (physes) at each end of long bones.

The? child is under general anesthesia. The? surgeon makes a cut over the growth plate at the end of the bone in the longer leg.
The growth plate may be destroyed by scraping or drilling it? to stop further growth at that growth plate.Another method is to insert staples on each side of the bony growth plate. These can be removed when both legs are close to the same length.

Metal pins, screws, staples, or plates may be used to hold the bone in place during healing. Most orthopedic surgeons prefer to wait several months to a year before removing any large metal implants. Removal of implanted devices requires another surgery using general anesthesia.

Why the Procedure Is Performed

Leg lengthening is considered if? person has large differences in leg length (more than 5 cm or 2 inches). Leg lengthening is more likely to be recommended:
For children whose bones are still growingFor patients who were short to begin with
Leg shortening or restricting is considered for smaller differences in leg length? (usually less than 5 cm or 2 inches). Shortening a longer leg may be recommended for children whose bones are no longer growing.

Bone growth restriction is recommended for children whose bones are still growing. It is used to restrict the growth of a longer bone, while the shorter bone continues to grow to match its length. Proper timing of this treatment is important to ensure good results.

Certain health conditions can lead to severely unequal leg lengths. They include:
PoliomyelitisCerebral palsySmall, weak? muscles or short, tight (spastic) muscles, which may cause? problems and prevent normal leg growthHip diseases such as Legg-Perthes diseasePrevious injuries or? broken bonesBirth defects (congenital deformities) of bones, joints, muscles, tendons, or ligaments

Risks for any anesthesia include:
Reactions to medicationsProblems breathing
Risks for any surgery include:
Additional risks include:
Bone growth restriction (epiphysiodesis), which may cause short heightBone infection (osteomyelitis)Injury to blood vesselsPoor bone healingNerve damage
After the Procedure

After bone growth restriction:
It is common for children to spend up to a week in the hospital. Sometimes a cast is placed on the leg for 3 to 4 weeks.Healing is complete in 8 to 12 weeks, at which time the child can restart full activities.
After bone shortening:
It is common for children to spend 2 to 3 weeks in the hospital. Sometimes a cast is placed on the leg for 3 to 4 weeks.Muscle weakness is common, and muscle strengthening exercises are started soon after surgery.Crutches are used for 6 to 8 weeks.Some children take 6 to 12 weeks to regain normal knee control and function.A metal rod placed inside the bone is removed at 1 year.
After bone lengthening:
The child will spend a week or longer in the hospital.Frequent visits to the doctor are needed to adjust the lengthening device. How long the lengthening device is used depends on the amount of lengthening needed. Physical therapy is needed to maintain normal range of motion.Special care of the pins or screws holding the device is needed to prevent infection.How long it takes the bone to heal depends on the amount of lengthening. Each centimeter of lengthening takes 36 days of healing.
Because the blood vessels, muscles, and skin are involved, careful and frequent checking of the skin color, temperature, and sensation of the foot and toes is important. This will help identify any damage to blood vessels, muscles, or nerves as early as possible.

Outlook (Prognosis)

Bone growth restriction (epiphysiodesis) is usually successful when it is done at the correct time in the growth period. However, it may cause short stature.

Bone shortening may be more exact than bone restriction, but it requires a much longer recovery period.

Bone lengthening is completely successful about 40% of the time. It has a much higher rate of complications.


Beaty H. Congenital anomalies of the lower extremity. In: Canale ST, Beaty JH, eds. Campbell's Operative Orthopaedics. 11th ed. Philadelphia, Pa: Mosby Elsevier;2007:chap 26.

Friedman JE, Davidson RS. Leg-length discrepancy.? In: Kliegman RM, Behrman RE, Jenson HB, Stanton BF, eds. Nelson Textbook of Pediatrics. 19th ed. Philadelphia, Pa: Saunders Elsevier; 2011:chap 668.

Version InfoLast Reviewed on 11/12/2012Neil K. Kaneshiro, MD, MHA, Clinical Assistant Professor of Pediatrics, University of Washington School of Medicine. Also reviewed by A.D.A.M. Health Solutions, Ebix, Inc., Editorial Team: David Zieve, MD, MHA, David R. Eltz, Stephanie Slon, and Nissi Wang.
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This page was last updated: May 31, 2013
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