Polydactyly is a condition in which a person has more than 5 fingers per hand or 5 toes per foot.
Extra digits; Supernumerary digits
Having extra fingers or toes (6 or more) can occur on its own. There may not be any other symptoms or disease present. Polydactyly may be passed down in families. This trait involves only one gene that can cause several variations.
African Americans, more than other ethnic groups, can inherit a 6th finger. In most cases, this is not caused by a genetic disease.
Polydactyly can also occur with some genetic diseases.
Extra digits may be poorly developed and attached by a small stalk. This most often occurs on the little finger side of the hand. Poorly formed digits are usually removed. Simply tying a tight string around the stalk can cause it to fall off in time if there are no bones in the digit.
In some cases, the extra digits may be well-formed and can even function.
Larger digits may need surgery to be removed.
Causes may include:
You may need to take steps at home after surgery to remove an extra digit. These steps may include checking the area to make sure the area is healing and changing the dressing.
Most of the time, this condition is discovered at birth when the baby is still in the hospital.
The health care provider will diagnose the condition based on a family history, medical history, and a physical exam.
Medical history questions may include:
Tests used to diagnose the condition:
You may want to make a note of this condition in your personal medical record.
Extra digits may be discovered the first 3 months of pregnancy with ultrasound or a more advanced test called embryofetoscopy.
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Mauck BM, Jobe MT. Congenital anomalies of the hand. In: Azar FM, Beaty JH, Canale ST, eds. Campbell's Operative Orthopaedics. 13th ed. Philadelphia, PA: Elsevier; 2017:chap 79.
Son-Hing JP, Thompson GH. Congenital abnormalities of the upper and lower extremities and spine. In: Martin RJ, Fanaroff AA, Walsh MC, eds. Fanaroff and Martin's Neonatal-Perinatal Medicine. 11th ed. Philadelphia, PA: Elsevier; 2020:chap 99.