Syndactaly is a congenital condition in which two or more toes remain connected because the digits did not fully separate during development. The connection is usually limited to skin (simple syndactaly), but in rare cases the bones, tendons, or blood vessels may also be fused (complex syndactaly).
Webbing occurs in approximately one out of every 2,000–2,500 births and is three times more common in males. The most typical presentation is partial webbing between the second and third toes, which is often inherited and usually harmless. Syndactaly may also appear as part of more than 300 genetic syndromes involving the skull, face, or limbs, and about half of all cases affect both feet.
Three primary types are seen in the foot: Type 1 (zygodactyly), involving the second and third toes; Type 2 (synpolydactyly), which includes both webbing and an extra toe; and Type 3, which is associated with fusion of the metatarsal bones. In some cases, the webbing extends only to the first joint, while in others it may run the full length of the toes.
Treatment is rarely necessary for simple syndactaly of the toes because it typically causes no functional problems. When surgery is performed, it is usually for cosmetic reasons. Separation requires skin grafting, and complex cases involving shared tendons or blood supply are more challenging. When an extra digit is present, removal is often recommended if the extra toe is on the inner or outer border of the foot; central polydactyly is more difficult to correct cosmetically and functionally.
Webbing of the fingers and toes is called syndactaly. It refers to the connection of two or more fingers or toes. Webbing usually only involves a skin connection between the two areas, but in rare cases may involve the fusion of bones. This is known as simple vs. complex webbing. What occurs here is a failure of two or more adjacent digits to fully segmentalize during development.
Webbing occurs once in every 2000-2500 births and is three times more common in males than females. Webbing may be discovered during an examination of an infant or child. In its most common form, it is seen as webbing between the 2nd and 3rd toes. This form is often inherited and is not unusual.
Syndactyly can also occur along with other birth defects involving the skull, face, and bones. In fact webbing of the toes may be associated with over 300 syndromes.
The web connections usually run up to the first joint of the finger or toe, but may run the entire length. Bilateral involvement is found in 50% of patients.
"Polysyndactyly" describes both webbing and the presence of an extra number of fingers or toes. The "location" of the extra digit goes a long way in determining treatment, if treatment is necessary.
In the foot three types of webbing are seen.
Type 1 (zygodactyly), partial or complete webbing of the second and third toes; hands may also be affected.
Type 2 (synpolydactyly), syndactyly of the lateral two toes and polydactaly of the fifth toe in the syndactyly web.
Type 3, associated with metatarsal fusion.
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Surgical intervention for simple syndactaly of the foot is rarely indicated as the webbing causes minimal loss of function of the toes, it is more of an issue with the fingers. Perhaps the number one reason for surgical intervention is cosmetic disapproval by the patient, rather than loss of function, at least in the foot.
Simple syndactaly involves skin grafts to separate the toes. If the two adjacent bones are fused separation becomes more difficult because many times there is only a single tendon and vascular system supplying the two toes and once separated obviously the two toes would no longer be able to share the tendon and blood supply.
In instances where you have a polydactyly (extra digit), if it occurs on the medial or lateral side of the foot, then amputation of the extra digit is the treatment of choice, assuming once again the extra digit does not share a common blood supply with the adjacent digit.
In patients that exhibit central polydactyly where the extra digit is in the middle of the foot, it becomes more difficult to determine which digit to surgically remove. However, removing the extra "inside" digit does not narrow the foot in any way and reconstruction of the middle of the foot in a cosmetically acceptable fashion can be very difficult.
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DISCLAIMER: The purpose of this site is purely informational in nature. It is not intended to diagnose, treat or cure any medical condition. This information is not a substitute for advice from a medical professional. Please consult your healthcare provider for accurate diagnosis and treatment. The information presented here may be subject to errors and omissions.
SITE LAST UPDATED: MAY 2026


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