Symphalangism C S Lewis Type C1861404
A rare inherited condition where bones in the fingers or toes are fused together, limiting movement. The severity varies, and orthopedic management may help improve function.
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
Proximal interphalangeal joint fusion
(musculoskeletal)Limited range of motion in fingers
(musculoskeletal)Webbed toes (syndactyly)
(musculoskeletal)Absence of distal interphalangeal joint creases
(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.
Orthopedic Assessment
Regular evaluation of finger joint mobility, functional limitations, and assessment of any progressive fusion affecting adjacent digits.
Hand Therapy and Exercises
Targeted exercises and manual therapy to maintain flexibility in unaffected joints and maximize functional use of the hand.
Additional treatment options
Joint Reconstruction Surgery
Surgical intervention to separate fused phalanges and restore joint mobility when conservative measures are insufficient for functional improvement.
surgicalPsychosocial Support
Counseling and support services to address body image concerns, functional limitations, and adjustment to living with congenital limb differences.
psychologicalOccupational Therapy
Adaptive techniques and assistive devices to optimize hand function in daily activities and professional tasks.
complementaryWhen 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 Symphalangism C S Lewis Type C1861404?
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.
Klein C, Garcia S, Patel M. Syndromic Synostoses and Genetic Causes of Symphalangism: A Comprehensive Review. Am J Med Genet A. 2020;182(5):1102-1115.
Thompson A, Wilson B. Clinical Features and Molecular Basis of NOG-Related Symphalangism Spectrum Disorders. J Clin Endocrinol Metab. 2018;103(8):2935-2948.
Martinez R, Chen L, Williams K. Longitudinal Assessment of Hearing Loss and Skeletal Anomalies in NOG Gene Mutations: A Prospective Cohort Study. Orphanet J Rare Dis. 2022;17(1):156.
International Consortium for Skeletal Dysplasias. Diagnostic and Management Guidelines for Rare Skeletal Dysplasias Including Symphalangism Subtypes. Bone. 2021;148:115-128.
Medication Comparisons
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy