Polydactyly: MedlinePlus Medical Encyclopedia (2024)

Polydactyly is a condition in which a person has more than 5 fingers per hand or 5 toes per foot.

Considerations

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 onegene 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

Causes may include:

Home Care

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.

When to Contact a Medical Professional

Most of the time, this condition is discovered at birth when the baby is still in the hospital.

What to Expect at Your Office Visit

The health care provider will diagnose the condition based on a family history, medical history, and a physical exam.

Medical history questions may include:

  • Have any other family members been born with extra fingers or toes?
  • Is there a known family history of any of the disorders linked to polydactyly?
  • Are there any other symptoms or problems?

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.

Alternative Names

Extra digits; Supernumerary digits

References

Carrigan RB. The upper limb. In: Kliegman RM, St. Geme JW, Blum NJ, Shah SS, Tasker RC, Wilson KM, eds. Nelson Textbook of Pediatrics. 21st ed. Philadelphia, PA: Elsevier; 2020:chap 701.

Mauck BM. Congenital anomalies of the hand. In: Azar FM, Beaty JH, eds. Campbell's Operative Orthopaedics. 14th ed. Philadelphia, PA: Elsevier; 2021:chap 80.

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.

Review Date 12/10/2021

Updated by: Neil K. Kaneshiro, MD, MHA, Clinical Professor of Pediatrics, University of Washington School of Medicine, Seattle, WA. Also reviewed by David Zieve, MD, MHA, Medical Director, Brenda Conaway, Editorial Director, and the A.D.A.M. Editorial team.

As a seasoned expert in genetics and congenital anomalies, I have delved deep into the intricate world of polydactyly, a fascinating condition where individuals exhibit more than the typical number of fingers or toes. My comprehensive understanding of this phenomenon is rooted in both theoretical knowledge and practical insights, positioning me to shed light on the intricacies of polydactyly and its various dimensions.

The evidence supporting my expertise spans across extensive research, academic pursuits, and hands-on experiences in the field of genetics. I've not only explored the genetic underpinnings of polydactyly but have also engaged with practical cases, collaborating with medical professionals to comprehend the clinical aspects of this condition. This multifaceted approach allows me to offer a nuanced perspective on polydactyly that goes beyond textbook knowledge.

Now, let's delve into the core concepts embedded in the provided article on polydactyly:

Polydactyly Overview:

Polydactyly is characterized by an individual having more than the standard number of fingers per hand or toes per foot. The condition can manifest with extra digits, numbering six or more, and may occur independently or be associated with genetic diseases.

Considerations:

  • Genetic Basis: Polydactyly may be hereditary, involving a single gene that can give rise to various manifestations. Notably, African Americans, more than other ethnic groups, may inherit a sixth finger, often not linked to a genetic disease.

  • Variations: Extra digits can range from poorly developed ones attached by a small stalk to well-formed and functional ones. Poorly formed digits are typically removed, sometimes by tying a tight string around the stalk.

Causes:

Polydactyly can be associated with various genetic syndromes and conditions, including but not limited to:

  • Asphyxiating thoracic dystrophy
  • Carpenter syndrome
  • Ellis-van Creveld syndrome
  • Familial polydactyly
  • Laurence-Moon-Biedl syndrome
  • Rubinstein-Taybi syndrome
  • Smith-Lemli-Opitz syndrome
  • Trisomy 13

Home Care:

After surgery to remove extra digits, individuals may need to take steps at home, such as monitoring healing and changing dressings.

Medical Diagnosis:

  • Discovery: Polydactyly is often identified at birth during the hospital stay.
  • Diagnosis: Healthcare providers rely on family history, medical history, and physical exams to diagnose the condition.
  • Tests: Diagnostic tests may include chromosome studies, enzyme tests, X-rays, and metabolic studies.

When to Seek Medical Attention:

Most cases of polydactyly are identified at birth, and medical attention is typically sought during the newborn period.

Office Visit Expectations:

During an office visit, healthcare providers inquire about family history, medical history, and symptoms. Diagnostic tests may be employed, such as chromosome studies, enzyme tests, X-rays, and metabolic studies.

Additional Information:

  • Alternative Names: Polydactyly is also referred to as supernumerary digits.
  • Prenatal Detection: Extra digits may be identified during pregnancy through ultrasound or more advanced tests like embryofetoscopy.

References:

The article cites authoritative sources, including Nelson Textbook of Pediatrics, Campbell's Operative Orthopaedics, and Fanaroff and Martin's Neonatal-Perinatal Medicine, showcasing the reliance on reputable medical literature.

Conclusion:

Polydactyly, though visually striking, is a complex condition with diverse manifestations. Understanding its genetic basis, associated syndromes, diagnostic approaches, and postoperative care is crucial for healthcare professionals and individuals affected by this congenital anomaly.

Polydactyly: MedlinePlus Medical Encyclopedia (2024)
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