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Syndactyly 

Syndactyly
Classification and external resources
New born baby hand showing complete complex syndactyly of two fingers.
ICD-10 Q70.
ICD-9 755.1
OMIM 185900 186100 186200 186300
DiseasesDB 29330
MedlinePlus 003289
eMedicine orthoped/563 
MeSH D013576

Syndactyly (from Greek συν- = "together" plus δακτυλος = "finger") is a condition where two or more digits are fused together. It occurs normally in some mammals, such as the siamang but is an unusual condition in humans.

Contents

Classification

Syndactyly can be simple or complex.

  • In simple syndactyly, adjacent fingers or toes are joined by soft tissue.
  • In complex syndactyly, the bones of adjacent digits are fused. The kangaroo exhibits complex syndactyly.

Syndactyly can be complete or incomplete.

  • In complete syndactyly, the skin is joined all the way to the tip of the finger
  • In incomplete syndactyly, the skin is only joined part of the distance to the fingertip.

Complicated syndactyly occurs as part of a syndrome (such as Apert's syndrome) and typically involves more digits and with complex syndactyly.

Fenestrated syndactyly means the skin is joined for most of the digit but in a proximal area there is gap in the syndactyly with normal skin. This type of syndactyly is found in amniotic band syndrome.

Simple syndactyly can be full or partial, and is present at birth (congenital). In early human fetal development, webbing (syndactyly) of the toes and fingers is normal. At about 16 weeks of gestation, apoptosis takes place and an enzyme dissolves the tissue between the fingers and toes, and the webbing disappears. In some fetuses, this process does not occur completely between all fingers or toes and some residual webbing remains.


Genetics

Five types[1] of syndactyly have been identified in humans. The corresponding loci associated with these types and their common phenotypical expression are as follows:

  • type I - 2q34-q36;[2] webbing occurs between middle and ring fingers and/or second and third toes.
  • type II - 2q31;[3] also involves long and ring fingers, but has a sixth finger merged inbetween.
  • type III - 6q21-q23; small finger is merged into the ring finger.
  • type IV - 7q36;[4] involves all fingers and/or toes

See also

Treatment

  • Timing- Syndactyly of the border digits (thumb/ index finger or ring/ small fingers) is treated at early age to prevent the larger digit from curving towards the smaller digit with growth. Typically, syndactyly of these digits is treated at 6 months of age. The treatment of syndactyly of the other digits is elective and is more commonly performed when the digits have grown, at 18- 24 months of age.
  • Techniques- Because the circumference of the conjoined fingers is smaller than the circumference of the 2 separated fingers, there is not enough skin to cover both digits once they are separated at the time of surgery. Therefore, the surgeon must bring new skin into the area at the time of surgery. This is most commonly done with a skin graft (from groin or anterior elbow). Skin can also be utilized from the back of the hand by mobilizing it (called a "graftless" syndactyly correction).
  • Complications- The most common problem with syndactyly correction is creeping of the skin towards the fingertip over time. This is likely due to tension at the site of the repair between the digits. Additional surgery may be required to correct this. One critique of using skin grafts is that the grafts darken in the years after surgery and become more noticeable. Also, if the skin grafts are harvested from the groin area, the skin may grow hair. Finally, the fingers may deviate after surgery. This is most commonly seen in complex syndactyly (when there has been a bony joining of the fingers).

References

  1. ^ Flatt A (2005). "webbed fingers". PMID 16200145. 
  2. ^ Bosse K, Betz RC, Lee YA, et al (2000). "Localization of a gene for syndactyly type 1 to chromosome 2q34-q36". Am. J. Hum. Genet. 67 (2): 492–7. doi:10.1086/303028. PMID 10877983. 
  3. ^ Sarfarazi, Akarsu, et al (1995). "Localization of the syndactyly type II (synpolydactyly) locus to 2q31 region and identification of tight linkage to HOXD8 intragenic marker". Hum. Mol. Genet. 4: 1453. doi:10.1093/hmg/4.8.1453. PMID 7581388. 
  4. ^ Sato D, Liang D, Wu L, et al (2007). "A syndactyly type IV locus maps to 7q36". Journal of Human Genetics 52 (6): 561–4. doi:10.1007/s10038-007-0150-5. PMID 17476456. 
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