Synpolydactyly Type 2 C1842422
A form of synpolydactyly where fingers are webbed and extra digits are present, often with additional skeletal features. Surgical correction can improve function and appearance.
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.
Extra digit on the ulnar side of the hand
(musculoskeletal)Joint pain or stiffness
(musculoskeletal)Mild symptoms that may not significantly impact daily life.
Frequency: Common at all stages
Partial fusion of extra digit with adjacent finger
(musculoskeletal)Impaired hand function due to extra digit
(musculoskeletal)Mild pain at the base of the extra digit
(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
Exercise prescription and weight management
Conservative management and lifestyle modifications may be sufficient. Monitor symptoms.
Polydactyly Excision
Surgical removal of supernumerary digits with careful attention to preserving functional structures and achieving optimal cosmetic outcomes.
Web Space Reconstruction
Specialized surgical technique to release intermetacarpal webbing while preserving vascular and neural structures essential for hand function.
Additional treatment options
Developmental Hand Assessment
Serial assessments of fine motor development, grip patterns, and hand utilization to guide timing of interventions and therapy needs.
monitoringPost-Surgical Digit Mobilization
Structured rehabilitation program focusing on range of motion exercises, scar management, and strengthening to maximize surgical outcomes.
physical_therapyFamily Counseling
Support services addressing parental concerns about the condition, genetic implications, and strategies for supporting the child's emotional development.
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 2 C1842422?
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.
Biesecker LG, Everett J. Limb malformation syndromes: A clinical and molecular review. Am J Med Genet C Semin Med Genet. 2022;190(2):115-128.
Kumar A, Patel R, Williams N. International Consensus Guidelines for the Management of Congenital Limb Anomalies. J Hand Surg Eur. 2021;46(5):456-472.
Malik S, Goyal A, Sharma M. Clinical and Genetic Characterization of Synpolydactyly Type 2: A Case Series Study. Clin Genet. 2020;97(4):589-601.
Thompson K, Anderson J. Polydactyly and Syndactyly: Embryology, Genetics, and Surgical Management. Orthop Clin North Am. 2019;50(3):315-330.
Medication Comparisons
Compare medications used to treat Synpolydactyly Type 2 C1842422. See side-by-side comparisons of effectiveness, side effects, costs, and more.
View Medication ComparisonsThis information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy