Polydactyly | |
Right hand with mid-ray duplication | |
ICD-10 | Q69 |
ICD-9 | 755.0 |
OMIM | 603598 |
DiseasesDB | 24853 |
eMedicine | derm/692 |
WikiDoc Resources for Polydactyly |
Articles |
---|
Most recent articles on Polydactyly Most cited articles on Polydactyly |
Media |
Powerpoint slides on Polydactyly |
Evidence Based Medicine |
Clinical Trials |
Ongoing Trials on Polydactyly at Clinical Trials.gov Clinical Trials on Polydactyly at Google
|
Guidelines / Policies / Govt |
US National Guidelines Clearinghouse on Polydactyly
|
Books |
News |
Commentary |
Definitions |
Patient Resources / Community |
Patient resources on Polydactyly Discussion groups on Polydactyly Patient Handouts on Polydactyly Directions to Hospitals Treating Polydactyly Risk calculators and risk factors for Polydactyly
|
Healthcare Provider Resources |
Causes & Risk Factors for Polydactyly |
Continuing Medical Education (CME) |
International |
|
Business |
Experimental / Informatics |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor-In-Chief: Cafer Zorkun, M.D., Ph.D. [2] Kiran Singh, M.D. [3]
Polydactyly or polydactylism (from the Greek poly = "many" + daktylos = "finger"), also known as hyperdactyly, is a congenital physical anomaly consisting of supernumerary fingers or toes. When each hand or foot has six digits, it is sometimes called "sexdactyly", "hexadactyly", or "hexadactylism". Although the condition is usually not life-threatening or even particularly debilitating, most people in Western societies have the extra digits removed surgically.
The extra digit is usually a small piece of soft tissue; occasionally it may contain bone without joints; rarely it may be a complete, functioning digit. The extra digit is most common on the ulnar (little finger) side of the hand, less common on the radial (thumb) side, and very rarely within the middle three digits. The extra digit is most commonly an abnormal fork in an existing digit, or it may rarely originate at the wrist like a normal digit does.
Polydactyly can occur by itself, or more commonly, as one feature of a syndrome of congenital anomalies. When it occurs by itself, it is associated with autosomal dominant mutations in single genes, i.e. it is not a multifactorial trait. [4] But mutation in a variety of genes can give rise to polydactyly. Typically the mutated gene is involved in developmental patterning, and a syndrome of congenital anomalies results, of which polydactyly is one feature.
The condition has an incidence of 1 in every 500 live births[1] although the frequency is higher in some groups (an example is the Amish in the United States, due to the founder effect).
Rudimentary polydactyly. Adapted from Dermatology Atlas.[2]
Rudimentary polydactyly. Adapted from Dermatology Atlas.[2]
Rudimentary polydactyly. Adapted from Dermatology Atlas.[2]
Rudimentary polydactyly. Adapted from Dermatology Atlas.[2]
Rudimentary polydactyly. Adapted from Dermatology Atlas.[2]
Rudimentary polydactyly. Adapted from Dermatology Atlas.[2]
Rudimentary polydactyly. Adapted from Dermatology Atlas.[2]
Rudimentary polydactyly. Adapted from Dermatology Atlas.[2]
Rudimentary polydactyly. Adapted from Dermatology Atlas.[2]
Rudimentary polydactyly. Adapted from Dermatology Atlas.[2]
Rudimentary polydactyly. Adapted from Dermatology Atlas.[2]
Left foot with postaxial polydactyly of 5th ray
Right hand with mid-ray duplication