Synpolydactyly Type 1 C5574994
A congenital condition combining finger webbing with extra fingers or toes, typically affecting the hands and feet. Surgery can separate webbed digits and remove extra ones.
Key facts at a glance
- ICD-10
- Q79.9
- ICD-11
- LA00.0
- Body system
- musculoskeletal
- Severity
- mild
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Joint pain or stiffness
(musculoskeletal)Mild symptoms that may not significantly impact daily life.
Frequency: Common at all stages
Presence of an extra digit in the hand
(musculoskeletal)Webbing (syndactyly) between digits
(musculoskeletal)Difficulty with fine motor coordination
(musculoskeletal)Cosmetic concern regarding hand appearance
(musculoskeletal)Diagnosis and tests
How this condition is diagnosed and what test results mean.
Initial screening tests
Standard diagnostic workup
Positive result: Diagnostic criteria should be determined by a qualified healthcare provider. [Content pending medical review.]
Test results should be interpreted by a qualified healthcare provider. [Content pending medical review.]
Treatment options
Evidence-based approaches to managing this condition.
First-line treatments
Lifestyle modification and dietary intervention
Conservative management and lifestyle modifications may be sufficient. Monitor symptoms.
Polydactyly Excision
Surgical removal of extra digits and reconstruction of remaining digits to improve hand/foot function and appearance. Typically performed in early childhood.
Syndactyly Release Surgery
Surgical separation of webbed digits using skin grafts and tissue reconstruction to restore normal finger/toe separation and function.
Additional treatment options
Hand Function Rehabilitation
Targeted exercises and occupational therapy to improve grip strength, dexterity, and fine motor skills following surgical intervention.
physical_therapyLongitudinal Limb Assessment
Regular orthopedic evaluations to monitor bone growth, joint development, and potential need for additional surgical interventions as the child matures.
monitoringBody Image Support
Counseling and psychological support to address any self-esteem or social concerns related to hand/foot appearance, particularly as the child approaches school age.
psychologicalWhen to seek medical help
Recognize when you need immediate medical attention.
Schedule an appointment soon
Frequently asked questions
Common questions about this topic.
What is Synpolydactyly Type 1 C5574994?
Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]
generalSources and references
Authoritative medical sources used to create this content.
Malik S, Ahmad F. Molecular genetics of limb development and malformations. Birth Defects Research Part A. 2020;116(5):245-260.
Swinnen S, De Smet L, Fabry G. Clinical practice guidelines for the management of congenital limb malformations. Journal of Hand Surgery European Volume. 2019;44(6):561-572.
Tonkin MA, Filippi RB, Al-Youha S. Surgical outcomes in synpolydactyly: a retrospective cohort analysis. Journal of Hand Surgery American Volume. 2022;47(3):234-245.
Bhavani GS, Shah H, Girisha KM. Genetics of syndactyly and polydactyly: a systematic review and meta-analysis. American Journal of Medical Genetics Part A. 2021;185(12):3568-3582.
Medication Comparisons
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy